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Project Coordinator, Clinical Research Administration In collaboration with the Senior Manager of Operations and Finance, Assistant General Counsel and management staff of Clinical Research Administration, the Project Coordinator assists in coordinating various aspects of assigned research and operations projects. Initiates workflows, collects data, manages contract assignments, presents findings and recommendations, disseminates information, and manages projects and project timelines. Responds to inquiries and acts as liaison to internal and external contacts. You Will:- Database and Information Management- Project Coordination- Administrative Coordination and LiaisonYou need:- A minimum of an Associate’s degree in Sciences, Liberal Arts, Health Administration, or other relevant programs- Bachelor’s degree with at least 2 years experience in a healthcare setting or supporting senior management preferred- Project coordination experience- At least 2 years administrative experience- Data management experience- Excellent verbal and written communication skills- Demonstrated ability to effectively manage multiple projects in order to meet deadlines- Proficient in MS Office package (including Outlook, PowerPoint and Excel) - Paralegal experience strongly preferred- Contract management experience strongly preferred#LI-Post
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ATTENTION INFUSION RN's!! Memorial Sloan Kettering Cancer Center Monmouth is seeking RN's to join our growing Chemotherapy team. You are:- An experienced Registered Nurse (RN) with recent/related oncology experience required including chemotherapy/biotherapy/immunotherapy administration.- Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.- A good decision-maker, with proven success at making timely decisions that maintain high standards of nursing care within the organization.- Actively seeking new ways to grow and be challenged, using both formal and informal development channels.- Approachable and comfortable with diverse groups of people and able to make others comfortable with you.- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.- Capable of building strong customer relationships and delivering customer-centric solutions. You will:- Manage a select caseload of patients receiving chemotherapy/biotherapy/immunotherapy on an outpatient basis.- Administer various therapies, perform patient assessments, provide symptom management and patient and family education.- Act as part of a multidisciplinary team provide continuity of care throughout various stages of treatment and follow-up.- Participate in the implementation of clinical support programs and quality assurance activities to ensure optimal care throughout the healthcare continuum. You need:- New Jersey Nursing Certification- BSN degree- 2 years of related chemotherapy/biotherapy/immunotherapy experience required- Chemotherapy certification highly preferred- Outpatient Oncology experience highly preferred Hours:- 12 hour shifts flexed 7:00a - 10:00p Monday - Friday. Weekend hours and (Float to all NJ Sites)
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We are seeking a Finance Manager to help manage digital and technology finances at MSK as we expand our digital capabilities. Situated within the Digital Informatics and Technology Solutions (DigITs) division you will be responsible for both internal divisional financial activities as well as tracking and reporting on IT spend outside of the division. This role offers tremendous growth opportunities and professional advancement. If you're looking to break into the technology field and have financial experience, apply now!You will!- Responsible for working with personnel throughout Memorial Sloan Kettering to budget and track IT program and project spending.- Act as a knowledge resource to guide appropriate budgeting of IT projects, ensure necessary information is captured, and prepare YOY baseline analysis of programs and projects.- Lead monthly financial review with all DigITs managers and obtain all related spend and forecast information.- Prepare and analyze monthly, quarterly, and annual divisional spend against budgets to identify problems, trends, and issues that require further review.- Responsible for cost analysis of IT products and services and providing recommendations on cost optimization opportunities.- Participate in system rationalization initiatives by providing cost breakdown for existing solutions.- Assist in developing IT finance training material, lead training sessions and educate DigITs managers on budget, forecast, and finance related topics.- Responsible for managing and coordinating resources to further improve the financial dashboard built on Tableau, as well as automating the current manual budgeting and cost tracking activities.- Assist in annual budget planning and preparation activities.You are!- Currently working as a financial manager or have relevant experience with financial management and analysis.- Great at working with financial data, budgets, reports, and analysis tools.- Independent worker who can prioritize work to meet established quarterly objectives and deadlines.- Highly detail and analytical thinker with an ability to conduct research, data analysis, and resolve complex problems with creativity and innovation in mind.- Familiar with or eager to learn new visualization and data analytic tools and techniques.- A great teammate with the ability able to build relationships and communicate effectively at all levels throughout MSK.- A Microsoft Excel expert You have!- A minimum of a Bachelor’s degree in Finance or Accounting or 8+ years minimum experience within accounting or financial management in lieu of a degree.- 6+ years of related experience in financial management- Experience with cost accounting, financial reporting, and budgeting.- Experience with IT costs and services performance analysis preferred but not required.- Significant experience with Microsoft Excel including working with advanced functions. Coding and writing macros not required.- Strong technical skillset, time management, multitasking, and organizational skills required.- Experience with data warehouse querying and data visualization tools such as Tableau, Cognos, or others is preferred.#LI-POST
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At MSK, we’re running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. We are seeking a Research Regulatory Associate (RRA) to join our Solid Tumor Thoracic service within the Department of Medicine. In this role, you will ensure the proper conduct of clinical research by developing, revising and maintaining accurate protocol tools at all times. - Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development.- Assist in protocol submission, drafting of consents, reviewing protocol logistics.- Assist in audits- reviewing and collecting regulatory documents for a high volume and fast-paced service.- House & maintain all CVs, medical licenses, certifications to ensure they are always current.- Participate in special projects and task forces as determined by management.- Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol.- Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed.- Assist in handling departmental data. Communicate with staff at all levels (principal investigators, clinical and research support staff).- Ensure that all appropriate regulations are followed throughout the course of a research project, database, or protocol. - Ensure that research protocols are approved by the Institutional Review Board and followed as written.- Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met.- Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested.- Provide leadership, organizational, creative, or clerical support to established and new research initiatives.- Provide support and report directly to Regulatory Research Manager - Exhibit excellent organizational skills and able to multi-task in order to meet deadlinesYou Are:- A good decision-maker, with proven success at making timely decisions that keep the organization moving forward. - Able to hold yourself and others accountable in order to achieve goals and live up to commitments.- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances. - Knowledgeable of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA).You Have:- A minimum of a High School Diploma with experience in clinical research or applicable experience.- A Bachelor’s degree is preferred.- At least 1 year of experience working in clinical research, preferably with experience in the regulatory spaceNote: - There will be some weekend work expectations to cover potential Serious Adverse Events (SAE) reporting. #LI-POST
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We are seeking a CT Technologist for our Breast & Imaging Center located at 300 E. 66th Street in Manhattan. This is a phenomenal opportunity to join a dynamic Radiology team.You are:• Committed to high standards of productivity.• Motivated to provide exceptional customer service.• Action-oriented and eager to take on new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.• Adaptable in your approach and demeanor in real time to match the shifting demands of different situations.• A good decision maker, with proven success of making timely decisions that keep the organization moving forward.• Adept at planning and prioritizing work to meet commitments aligned with organizational goals.• Able to use specialized knowledge and job-related experience to handle complex work assignments and/or provide guidance to other less experienced staff. You will:• Perform a variety of C.T. imaging procedures that require independent judgment and ingenuity with minimal supervision, on patients of all age groups.• Operate CT scanners and associated equipment safely and in accordance with established policies and practices.• Explain procedures to patients, monitoring for patient safety and comfort, administering contrast (IV and/or Oral).• Conduct imaging in accordance to established protocols and quality standards.• Enter complete and accurate documentation into all MSK/Radiology systems. You need:• Associate’s Degree / Certified Vocational Training or Graduate of a 2 yr AMA approved Radiology school.• ARRT in Radiography and C.T.• NYS Department of Health License in Diagnostic Radiography, IV Certification.• BLS Certification Hours:• M-F, 10 am to 6 pm#LI-POST
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Start your career at Memorial Sloan Kettering and you’ll find yourself quickly making a difference in the lives of our patients. When you join us as a Care Coordinator I at our new Nassau facility, you will find meaningful work and become part of a team where everyone plays an important role in the fight against cancer. Are you ready to make a difference in the lives of others? This is a life’s calling.YOU ARE:- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding- Adept at building partnerships and working collaboratively with a team to meet shared objectives and goals- Actively seeking new ways to grow and challenge yourself, using both formal and informal development- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances- Passionate about working in a healthcare setting and committed to delivering a best-in-class patient experience YOU WILL:- Work as a member of practice staff team of session assistants to ensure that each physician practice session is well-prepared, organized, and fully utilized and that each patient visit occurs with satisfaction- Serve as a liaison between the patient, family, and clinical team during the clinic visit- Greet/check-in and orient patients to the outpatient visit and to the environment, as well as complete the patient visit by scheduling and coordinating all appropriate tests, procedures, visits, treatments and consultations in accordance with the physicians’ ordersYOU HAVE:- An associate’s or 2 years college (required); bachelor’s degree (preferred). A high school diploma/GED and 2 years relevant experience (frontline, patient-facing role in healthcare) in lieu of the associate’s degree.- A proven dedication to healthcare through work, internship, or volunteer experience.- Excellent computer skills- Ability to handle acutely ill patients in stressful situations with a positive demeanor- Ability to provide at least a 2 year commitmentHours vary between 6:15am and 10:00 pm (Monday-Friday, occasional Saturdays). Schedules are provided a week in advance. Must be flexible to work anytime during this timeframe. The initial three week training period for the Care Coordinator role will take place in Manhattan. After completing our quick online application form, you will complete a profile assessment on our partner site, Pymetrics. It should take you about 25-30 minutes to complete. IMPORTANT - Please make sure you click on the return to application button after completing the assessment to complete your application. Note; If you already have a Pymetrics account under this email for a different application, login with your existing account. Please do not make a new account. If you are on mobile, download the Pymetrics mobile app (pymetrics.com/downloads). #LI-POST
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Do you want to be a part of something bigger than yourself? At MSK, we’re running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. Spend some time with us and explore how you can find your life's calling as a Clinical Research Coordinator at MSK. Wednesday, March 25th from 4:30 pm – 7pm in New York City During the Information Session you will:- Meet with members of our Clinical Research team and learn why they've built their careers at MSK- Connect with Clinical Research Managers and discover what they look for in their new team members- Learn about what makes MSK one of Glassdoor's "Best Places to Work", including resources and training to help our staff advance their careersWe are seeking experience Clinical Research Professionals for a variety of roles within our team! As a Clinical Research Supervisor, you will: - Staff Management and Development - Participate in the orientation, training and supervision of CRCs; participate in facilitating departmental trainings; align staff and resources with appropriate protocols and research needs; and maintain workflow consistency among staff with standardized processes.- Operation Management - Ensure that workflow is managed and monitored to meet departmental and service needs; assist the Clinical Research Manager (CRM) with protocol activation, especially with start-up activities; monitor research portfolio for workload by appropriately managing and identifying service needs.- Quality Assurance - Perform regular audits to ensure that the data collected is complete and accurate, and that the research project is carried out as planned.- Regulatory Compliance - Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Also, you will ensure that research protocols are approved by the Institutional Review Board/Privacy Board (IRB/PB) and followed as written.- Data collection - Utilize appropriate methodologies to collect patient/human subject information for research projects, databases, and/or protocols.- Data reporting - Generate reports to all necessary parties (institutional and federal) on the progress. You will prepare data for analysis, monitoring visits and audits.- Clinical Research Billing Management - Implement Principal Investigator's decisions regarding Patient-Care Costs (both billable and non-billable), and ensures that research non-billable services are not billed to patients/human subjects or insurers. Also, you will assist manager with billing reconciliation.- Special Projects - Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. You will provide leadership, organizational, creative, or clerical support to established and new research initiatives.As a Research Regulatory Associate, you will: - Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development.- Partners with Clinical Research Associate to be made aware of protocol amendments and amends protocol tools as required.- Assist in audits- reviewing and collecting regulatory documents.- Maintains comprehensive, GCP/FDA compliant, regulatory files/binders for protocols. This includes, but is not limited to, collection and maintenance of the FDA Form 1572, Financial Disclosure Forms, Delegation of Authority logs, training logs, laboratory reference ranges and CLIA documentation, CVs and Licenses, Investigator Brochures, and Safety reports.- Participate in special projects and task forces as determined by management.- Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol.- Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed.- Ensure that all appropriate regulations are followed throughout the course of a research project, database, or protocol. - Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested.- Provide leadership, organizational, creative, or clerical support to established and new research initiatives.As a Research Project Associate, you will: - Participate in special projects and task forces as determined by management.- Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol.- REDCap database set-up; quality control; transfer to dataset for analysis.- Basic descriptive data analysis via SPSS, SAS, STATA, or other computer package; work with research team members on more complex data analyses.- Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed.- Assist with high-level departmental projects requiring data management support; provide data entry solutions as needed.- Communicate with staff at all levels (principal investigators, clinical and research support staff).- Perform regular audits to ensure that the data collected is complete and accurate and to ensure that the research project was carried out as outlined.- Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol.- Ensure that research protocols are approved by the Institutional Review Board and followed as written.- Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and creates processes to ensure that goals are met.- Participate or coordinate on both interdepartmental and intradepartmental organization-wide research projects as requested.- Provide leadership, organizational, creative, or clerical support to established and new research initiatives.As a Clinical Research Associate, you will:- Serve as the main point of contact for all research portfolio activities, and maintain real-time knowledge of every aspect of all research protocols. - Be the critical facilitator for a multidisciplinary team encompassing data and patient management, as well as regulatory oversight. - Effectively communicate the overall study progress to various internal and/or external stakeholders, and identify study trends and create/implement solutions. - Perform diverse research-related functions using sound judgment and exceptional organizational skills.- Anticipate and prioritize work to meet commitments of multiple stakeholders.- Be responsible fort building partnerships and working collaboratively to influence others to meet shared objectives and goals.- Serve as someone who improves processes and proactively, independently identifies solutions that anticipate stakeholder needs.To qualify to attend this event, you need: - A Bachelor’s degree OR a high school diploma and 2 years of research experience- Effective communication, excellent attention to detail, strong information and time management, and administrative / computer Skills- Flexibility in your approach and demeanor to align with the shifting demands of evolving circumstances Pre-register for this event by clicking 'Apply' now. Please note, space is limited and guests attendance will be confirmed by March 18th, 2020. Registration begins at 4pm. There is no need to arrive early. #LI-POST https://youtu.be/9R7QoNfmm0w
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The aim of the Flow Cytometry Core Facility is to help advance the scope and quality of Cancer Research at MSK by providing investigators advanced instrumentation and high-level technical and scientific expertise in multi-dimensional Flow Cytometry and Cell Sorting. We are currently seeking a Scientific Research Lead. The Scientific Research Lead's main responsibility is to act as the Scientific Manager by promoting, coordinating, and overseeing all scientific aspects involving the Core Facility. The role involves a close collaboration with the Operational Core Manager with overlapping duties and concerted strategies to manage the Core Facility. The Scientific Research Lead will be instrumental in maintaining high scientific standards in the Core Facility, by interacting with researchers as well as laboratory staff to establish collaborative projects across a range of scientific and technical disciplines. You will: - Consult with investigators, technicians, and students to suggest techniques and protocols relevant to the experimental questions and to ensure that experiments are optimally planned- Provide technical and scientific support in flow cytometry from experimental troubleshooting to data analysis- Assist with interpretation of data, assurance of data validity, and assurance that publications and presentations using data acquired in the core facility are accurate and appropriate- Assist and supervise core staff to ensure best experimental practices, as well as keeping the lab abreast of new technologies and flow cytometry applications - Assist in Education & Training of researchers and core staff, including development of new material- Develop, design, and conduct projects or experiments within the core’s scope. Coordinate data collection and analysis. Review progress and evaluate results- Maintain and establish new collaborations with other laboratories and core facilities, which may result in co-authoring publications and co-presenting results with other groups, as well as in national or international meetingsYou have: - Doctorate with 2-4 years of sound research experience; - Solid experience in Flow Cytometry, including strong expertise in multicolor panel design and implementation (good knowledge in best practices, instrument setup, and multiparameter data analysis)- Prior experience in Cancer Biology preferred. #LI-POST
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The aim of the Flow Cytometry Core Facility is to facilitate and help advance the scope and quality of Cancer Research at MSK by providing investigators advanced instrumentation and high-level technical and scientific expertise in multi-dimensional Flow Cytometry and Cell Sorting. We are currently seeking a Flow Cytometry Specialist with advanced Flow Cytometry experience to integrate an exciting team of scientific and technologically-driven staff. As a Flow Cytometry Specialist you will:- Operate cell sorters and perform simple troubleshooting and repairs of Flow Cytometry equipment- Provide technical and scientific support to researchers in operating analyzers and Flow Analysis software- Perform daily startup and shutdown of flow instrumentation- Perform daily cleaning and maintenance of flow instrumentation- Perform Quality Control in all Cell Sorters, Analyzers and other required instrumentation- Perform some Administrative duties- Assist in Research and Development programs coordinated by senior staff, and learn how to coordinate these programs independently- Learn Experimental Design and Execution in Flow CytometryAs a contributor to the Research and Development programs, you will have the opportunity to present your results in the Core Lab meetings, in Regional and/or International meetings, as well as co-authoring any publications resulting from your contributions. Requirements:- Bachelor’s Degree with 4-7 years experience operating in a Flow Core Facility or demonstrated experience in using Flow Cytometry. Master’s degree preferred. ##LI-POST
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We Are:MSK conducts one of the world’s largest clinical cancer research programs with patients and researchers typically involved in more than 900 total clinical trials at any given time. Teams of scientists and clinicians are united in a common pursuit: to transform our understanding of cancer and how we care for those affected by the disease.Clinical Trials Nurses (CTNs) integrate their expertise into the care of clinical trial participants, ensuring compliance with protocol procedures, assessments, and symptom management. Most importantly, the CTN acts as patient advocate, ensuring adherence to ethical practices during the conduct of clinical trials to protect the rights and well-being of patients and the collection and reporting of quality data. We contribute scientific knowledge, critical thinking skills, and care coordination to the interdisciplinary team and support early phase clinical trials where timely translation of research evidence into practice is an integral part of the MSK research mission.Our highly skilled, Magnet® recognized nursing team at Memorial Sloan Kettering (MSK) is comprised of over 4,000 nursing professionals. We are dedicated to delivering excellence in the art and science of professional nursing, consistent with our Mission, Vision and Values: MSK Nursing MissionWe provide compassionate, evidence-based nursing care to patients and families living with cancer in a healing and innovative environmentMSK Nursing VisionWe strive for excellence and leadership in patient care, education and researchMSK Nursing ValuesCompassion, Advocacy, Relationships, ExcellenceAre you ready to join our world renowned Nursing Team?You Are:- A progressive Nurse Leader who applies knowledge of the clinical nursing research landscape to advance the goals of MSK Nursing - An innovative, creative thinker who paints a compelling picture of the vision and strategy that motivates others to action - A motivator who creates a climate where people are empowered to do their best to help the organization achieve its objectives - A coach that can develop others to meet both their career goals and that of the Center - A builder of strong teams that apply their diverse skills and perspectives to achieve a common goalYou Will:As the Director of Clinical Trials Nursing at MSK, you will manage a team of Research Nurse Leaders responsible for operations and management of the Memorial Sloan Kettering Clinical Trials Nursing team. This team collectively provides study management and support to principal investigators overseeing clinical trials. As an integral member of executive nursing leadership and hospital, departmental and disease management research teams, you will work to refine and enhance the actualization of clinical trial nursing roles, and to communicate and achieve clinical research nursing goals and milestones in support of our expanding research portfolio. This position will work within multi-disciplinary teams across MSK to ensure that the requisite organizational clinical trials nursing infrastructure and resources are in place and optimally managed to achieve research protocol objectives. Responsibilities include, but are not limited to: - In alignment with a hospital and nursing strategic goal to continually improve Quality of Care and Patient Experience, work to facilitate integration of clinical trials research nursing into protocol study teams- Interact with Principal Investigators and clinical research teams to ensure study management needs are being met and consistently holding patients, families and staff as highest priorities- Develop policies, procedures, standards and systems to improve efficiency, quality and ensure compliance with clinical trial design and human subjects protection- Lead all aspects of clinical trials research nursing staff workloads, assure accuracy of study budgets with regard to inclusion of clinical research nursing time and effort, and develop quality improvements metrics for clinical trials nursing conduct and practice to enhance efficiency and clinical compliance- Interprets changes to the regulations and/or issuing of new guidance by the federal agencies as it relates to clinical research nursing across the Center. Evaluates and applies the changes as required. Alerts appropriate individuals if new/amended guidance and regulations will impact on current practice and procedures; assists with modifications as required- Foster an environment of continuous learning and scientific inquiry. Ensure that clinical research nurses are highly competent and possess in-depth knowledge related to research conduct and coordination. Motivate and support career progression and organizational citizenship consistent with the nursing professional practice model and the organizational mission of excellence in clinical research. You Need:This role requires a NYS RN License, Graduate Degree in Nursing, and a minimum of ten (10) years progressive leadership experience and clinical research experience required. Doctorate degree and oncology background are highly preferred. Clinical research-related certification and/or Oncology nursing certification required. #LI-JR1
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We are:At Memorial Sloan Kettering, we take a team approach to caring for children, adolescents, and young adults with cancer. Our experts share the goal of curing child and returning him or her to a life focused on family, friends, and the future. We care for young people with all types of cancer, from the most common to the rarest, and at any stage, including a cancer recurrence. You are:- Capable of building strong customer relationships and delivering customer-centric solutions.- Adept at creating partnerships and working collaboratively with others to meet shared objectives and goals.- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.You will:- Provide Child Life services to pediatric patients based on an understanding of child development and the impact that illness, injury, disability and hospitalization have on this process.- Develop and execute group activity programs- Plan interventions specific to the impact of the health care- Provide guidance for the family in understanding and dealing with hospital regulations and procedures, while facilitating opportunities for parents for actively continue their parenting role.- Maintain records, statistics, activity calendars, schedules, and other appropriate documentationYou have:- Bachelor’s degree in Child Life, Recreation Therapy, Art Therapy, or Special Education; Master’s preferred- 1-2 years of related experience- Child Life Specialist Certification OR completed requirements with plans to take exam within one year of hire Hours will vary between 8:00am-7:00pm and include a weekend rotation, as well as some holidays #LI-POST
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Clinical Nurse Specialist (CNS)-Inpatient Acute Care12 hour nights with a varied work schedule Are you an accomplished and proud Clinical Nurse Specialist? The expertise, creativity, commitment, and generosity of spirit of the men and women of Memorial Sloan Kettering are at the heart of our success. We are encouraged by one another’s dedication and compassion, and recognize the work being done in the service of our patients and our mission.New programs and state-of-the-art facilities are essential to our continued growth and achievement. But it is the people who work within our hospital, clinics and laboratories who truly ensure the future of MSK. And it is our patients who provide the inspiration for everything we do. WE ARE:At Memorial Sloan Kettering Cancer Center (MSK), we recognize and champion the role of the Clinical Nurse Specialist and the value it adds to our organization in meeting the specialized needs of our patients with cancer.Our amazing nursing team includes over 40 Clinical Nurse Specialists and we are growing the team. Are you ready to find your calling and make MSK your next career move? Our CNS’s are dedicated to ensuring quality and excellence in the art and science of professional nursing practice. This is consistent with our mission to provide compassionate, evidence-based nursing care to patients and families living with cancer in a healing and innovative environment.YOU WILL:- Utilize the tenets of primary nursing: knowledge, accountability, and continuity to foster a culture and structure supportive of caring and therapeutic relationships between nurses and patients and families- Inspire a culture of excellence and accountability by setting clear goals, expectations and benchmarks for performance- Contribute to the design, development and implementation of strategic and operational initiatives.- Lead and support staff during periods of transition; communicate purpose and empower staff to embrace change.- Demonstrate understanding and ensure the specific needs and care requirements of patient population are met.YOU ARE:- A good decision-maker, with known to work at making timely decisions that keep the organization moving forward- Able to work effectively in an environment notable for complex, sometimes contradictory information- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances- Effective at gaining the support and dedication of others by engaging them around your point of view and priorities Requirements:- Current New York State RN license with CNS qualification required- MSN- 3+ years of related experience- Experience in an advanced nursing role strongly preferred- Self-direction and strong interpersonal skills are essential Memorial Sloan Kettering’s (MSK) benefits program acknowledges the care that our employees put into their jobs every day. The program provides benefits, tools, resources and services to help employees at work, and in their lives outside of work. MSK is committed to providing a comprehensive benefits package to its employees. #LI
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We are: The Exercise Oncology Service (Ex-Onc) conducts clinical trials to study the efficacy of structured exercise training interventions on cardiovascular outcomes in individuals before and during cancer treatment, as well as following the completion of therapy, across a broad range of cancer diagnoses.The second major focus of our program is investigating whether exercise training is an effective treatment for cancer. We adopt traditional laboratory approaches to elucidate the effects and underlying mechanisms of exercise training on cancer progression as well as to determine whether exercise alters the response to conventional and novel cancer therapeutics. This information allows us to design more-effective clinical trials that test a precise “dose” of exercise in selected patient populations most likely to benefit from exercise training. You are:- Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.- Adept at creating partnerships and working collaboratively with others to meet shared objectives and goals.- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.- Actively seeking new ways to grow and be challenged, using both formal and informal development channels.You will:- Conduct pre-participation screening and administration of health and fitness assessments.- Assist in the administration of resting as well as exercise based assessments as required by the specific Ex-Onc protocols (e.g., CPET, Bruce, 1RM, YMCA)- Identification of symptom changes/signs of exercise contraindications and initiates the appropriate medical response and processes.- Utilize appropriate monitoring techniques and technologies to optimize physiologist testing and/or training sessions by assess resting and exercise vital signs and symptoms, including heart rate, electrocardiogram, blood pressure and oxygen saturation- Operate EKG equipment, exercise ergometer, blood pressure cuff, stethoscope, saturation monitor and/or metabolic measurement system.- Correct preparation, participant set-up and clean-up of metabolic measurement system- Calibrate, operate and maintain exercise training equipment (e.g., treadmill, ergometers, sphygmomanometer, scales, heart rate monitors, resistance machines).- Implement and effectively monitor protocol-specific exercise training sessions either onsite of via our Tele-Exercise approach.- Understand and support Exercise Oncology Service research protocols, clinical procedures and proficiency in facilitating protocol-specific physiological testing and exercise training.- Support the implementation of data collection methods for valid and reliable research.- Monitor overall safety and cleanliness of exercise training location, reporting significant issues, equipment and process concerns to the EPS.- Implements MSKCC standards as it relates to care and caution in protection confidential and sensitive information related to participants, personnel and staff.You have:Required:- A Bachelor’s degree in Exercise Science or related field- 2 + years of professional or practical educational experience (ie: internship) in exercise prescription implementation and individualized exercise training in special populations- Excellent written and verbal communication skills- The ability to accurately measure resting and exercising heart rate, blood pressure, oxygen saturation and subjective measures of intensity (ie: RPE, Dyspnea, etc)- The ability to conduct a safe exercise training session, ensuring appropriate monitoring of physiological parameters and providing encouragement and support throughout a session - American Heart Association (AHA) Basic Life Support, American College of Sports Medicine (ACSM) Certified Personal Trainer, National Strength and Conditioning Association (NSCA) – Certified Strength and Conditioning Specialist, or Sport or exercise coaching certification a plusPreferred:- 2 + years of exercise stress testing or cardiopulmonary exercise testing - 1 + years of experience in exercise stress testing or cardiopulmonary exercise testing Exposure to vascular testing (ie: flow mediated dilatation or pulse wave velocity) Position Hours: Monday-Friday; Flexibility is needed between 7:00am-8:00pm #LI-POST
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We Are:We’re taking bold steps to redefine what’s possible in Laboratory Medicine. Our state-of-the-art clinical laboratories provide sophisticated technology and automated equipment that allow our teams to get to answers faster and more efficiently, with a strong emphasis on applied and translational research. We are committed to the growth and advancement of the department, and fully support the active collaboration of scientists, clinicians and industry experts to develop next-generation laboratory methods. MSK is also dedicated to providing diverse educational opportunities to further develop the skills and ambitions of our medical technologists, laboratory managers, and laboratory directors. We are currently seeking an experienced Lab TechnologistsII for our Main Hospital - Rapid Results Lab.You will: - Perform technical duties in laboratory sections, with minimal supervision- Follows all laboratory procedures documented in the Standard Operating Procedures Manual when performing testing, thoroughly and accurately.- Performs technical procedures according to the required laboratory workflow patterns and in an organized manner so as to facilitate follow-up by other staff.- Consults with supervisor or senior technologist to verify procedure for specimens that do not follow SOPs. Contacts clinician to get additional information. Discusses alternatives with lab management and/or attending.- Verifies patient identification at all steps of every procedure. Maintains complete accuracy.- Performs all mathematical calculations, accurately, when necessary.- Maintain complete, accurate, legible, neat, organized, up-to-date records/logs/files- Assures the accuracy of all tests performed by adhering to the laboratory’s Standard Operating Procedures. Performs routine and advanced equipment maintenance- Contribute to the upkeep and safety of the laboratory and assures a clean, safe, adequately supplied work area. Maintains adequate inventories of reagents and supplies. Manage the physical environment of the laboratory in accordance with New York State DOH, Joint Commission, OSHA and CLIA regulations- Provide direction, training, and feedback on routine laboratory procedures, as assigned You need:- Bachelor's Degree in Medical Technology or Clinical Lab Sciences required- 2+ years of experience required- A NYS State Clinical Lab Technologist license required- ASCP Medical Lab Scientist preferredHours of work:- 37.5 hours per week- M-F, evening shift 4pm - 12am.
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The Digital Solutions department at MSK is seeking an individual with strong communication skills and technical competencies for the position of Robotic Process Automation Developer, in the Business Systems Group. Under the direction and guidance of the groups Senior IS Manager, this position will design, document, develop and deploy RPA solutions using the UiPath platform and oversee production support and maintenance. Are you a visionary ready to play a lead role in the next wave of technical innovation to further enhance the experience for our patients and employees? We are seeking an innovative, collaborative, forward-thinking, flexible, and user-focused developer to bring energy, creativity, and expertise to our team. The position develops, codes, tests, debugs, and documents new software or enhancements to existing software and typically works with staff from the functional and technical teams, as well as automation vendor - UiPath. The successful candidate will have the opportunity to participate in the Digital and Robotics Automation journey at MSK and work with various modules within, and integrated with the UiPath platform, and to plan, coordinate, and lead assigned projects.He/she is expected to work independently with minimal instruction/supervision and be willing to learn new technologies/systems.You Will:- Design, code, integrate, test, implement and maintain robotics applications (using RPA tool UiPath) according to business requirements.- Ability to gather business specifications and technical requirements, and translate them into robotic solutions creating well structured, maintainable and easy to understand Solution Design Document (SDD) or Technical Design Document (TDD).- Excellent written, verbal and interpersonal communication skills.- Ability to work in a team setting, as well as independently.- Ability to prioritize assignments and work in a fast-paced environment.You Are:- Bachelor’s Degree in Computer Science and 2-4 years’ experience in Information Systems, Healthcare preferred.- 2+ years of Development experience in any programming language such as .Net C#, JavaScript, Java- 1+ year hands on developing RPA solutions with Ui Path- Experience of working within an Agile SDLC in a continuous integration environment (Knowledge of SAFe, Scaled Agile Framework a plus)- Experience with AI/ML technologies preferred.- Experience with SQL, Splunk#LI-POST
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We are seeking an individual with a creative and analytical mind to join Sloan Kettering Institute’s Single Cell Research Initiative (SCRI). The SCRI team accelerates biomedical discovery through the application of state-of-the-art algorithms to single-cell genomics datasets collected from patient data and from advanced mouse and organoid models of cancer. The individual will help to develop computational methods and apply them to the flood of cutting-edge data being generated at SCRI to explore questions of tumor heterogeneity, drug-resistance, tumor stem-cells, mechanism of immunotherapy, the emergence of metastasis and the tumor-immune environment. SCRI bioinformatics is embedded in the group of Dr. Dana Pe’er, a leader in single-cell data analysis, providing guidance and a highly stimulating intellectual environment for analytical methods development. You should have a background in human biology with a minimum of some computer science and statistics courses, and you should be excited to learn how to apply sophisticated algorithms to big biological data at one of the top cancer research institutes in the world. Your implementation of processing and visualization algorithms will allow data scientists, biologists and clinicians to interact with and interpret the data. A key focus is the single-cell profiling of patient samples, with the goal of improving immunotherapy and precision medicine. Join us if you are eager to learn and want to make an impact! In this position, you will:- Implement, apply, and evaluate methods to process, normalize, organize and visualize single-cell sequencing data.- Provide initial analysis and biological interpretation of data- Prepare Python notebooks for interactive engagement with the data- Provide consultation, guidance and training to research scientists using SCRI tools Requirements:- Bachelor’s or Master’s degree with core biology and computer science courses- Analytical, reasoning, statistical, mathematical and problem-solving skills- Excellent written and verbal communication skills with biologists- Knowledge of programming language, preferably Python Preferred Qualifications:- Familiarity with high-throughput sequencing data- Programming experience (data analysis pipelines, high-performance computing)This position can begin as late as summer 2020.#LI-POST
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Memorial Sloan Kettering Cancer Center is seeking a Clinical Research Supervisor (CRS) for the Radiation Oncology Department. As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Supervisor (CRS) manages the day-to-day activities of the Clinical Research Associates (CRAs) and Clinical Research Coordinators (CRCs) at the department level ensuring efficient and effective operations. The CRS is responsible for data management activities, data integrity, and regulatory compliance associated with clinical research for the Radiation Oncology Department, and oversees the data collection and analysis for research projects, databases, and research protocols within MSK. The CRS also participates in special projects and task forces as determined by management.You are:- An analytical and critical thinker, comfortable making quality decisions independently.- Resourceful, curious, confident and eager to manage a wide variety of situations and tackle problems with minimal oversight.- Customer focused with strong communication skills.You will:- Work with the Clinical Research Manager, other Clinical Research Supervisor(s) and Program Manager to oversee the Radiation Oncology clinical research portfolio including prospective clinical trials and special projects.- Collaborate with clinical teams to coordinate research activities across various departments and multiple locations, according to institutional and other governing policies.- Implement all aspects of research protocols/projects from study start up to study closure.- Direct staff management and development of Clinical Research Associates (CRAs) and Clinical Research Coordinators (CRCs). Train and onboard new CRAs and CRCs, conduct routine one-on-one meetings with direct reports (CRAs and CRCs), oversee CRAs’ and CRCs’ workload and assist with prioritization, provide constructive feedback on performance, and offer professional growth and development guidance.- Implement standards for research databases and/or study management, and policies and procedures to meet those standards, to ensure the highest quality management of research projects and databases.- Generate reports and perform advanced queries for Principal Investigators, the IRB, sponsoring agencies, and management as requested.- Oversee data collection, entry and quality assurance tasks for research databases such as the Clinical Research Database (CRDB), Medidata Rave and other external electronic data capture systems.- Conduct systematic audits of research studies and/or databases to ensure that regulatory files are current and organized, and data collected has no typographical errors, is consistent with source documents, and is in compliance with external sponsor/regulatory requirements.- Facilitate biweekly team meetings and other PI/research/service-specific meetings as needed.- Develop and implement ongoing continuing education activities for research staff.You need:- At least 3 years of relevant (clinical research) experience (2 years with Masters), or as determined by hiring manager.- Or A minimum of a High School Diploma with at least 3 – 4 years MSKCC clinical research experience.- A Masters degree is preferred.- At least one year of supervisory experience strongly preferred.- Team leadership and mentoring experience.- Strong familiarity with computer systems, databases, and data reporting is preferred. A strong ability and understanding on how to collect, analyze, interpret and prepare data for presentation (i.e., written, tabular and graphical formats).- Excellent problem-solving abilities to analyze situations, draw conclusions, make recommendations, and convey this information in a timely and proficient manner.- Knowledge of GCP and ICH guidelines, FDA regulations, and Clinical Research Policies including Data Management, Quality Assurance, Clinical Trial Coordination and Monitoring.
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MSK is seeking a Radiology Application Analyst to support staff in the use of the PACS (Picture Archiving and Communication System), ASR (Automatic Speech Recognition) and other Radiology applications. THIS POSITION WILL SIT IN LONG ISLAND & NEW YORK CITY 50/50 SPLIT! Location 1: 650 Commack Road, Commack New York Location 2: 1114 1st Avenue, New York NY You Will:- Provide application support for radiology systems including, but not limited to, PACS, RIS and Voice recognition.- Use Remedy ticket tracking system for daily monitoring, troubleshooting and maintenance of Radiology Systems.- Participate in implementations and application upgrades of new and existing Radiology Systems.- Provide end-user training with users at all levels. Comfortable interacting with customers.- Coordinate with vendors to provide application and hardware support.- Assist with new modality installs including testing and connectivity to the PACS system.- Provide rotating on-call coverage after hours and on weekends.You Are:- Capable of building strong customer relationships and delivering customer-centric- A good decision-maker, with shown success at making timely decisions that keep the organization moving forward.- Able to work effectively in an environment notable for complex, sometimes contradictory- Willing to take action and eager to adopt new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.- Adept at building partnerships and working collaboratively with others to meet shared objectives and goals.- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.- Adept at learning quickly, applying insights from past efforts to new situations.- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances.You Need:- Bachelor’s Degree; degree in healthcare informatics, IT, or hospital administration preferred- 2-4 years experience in the field- Working knowledge of PC hardware, network technology, Windows operating system- Experience working in a hospital/clinical related department preferably in Radiology - Expectation of providing a high level of customer service#LI-POST
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The Radiopharmacy Technician is a technically skilled individual that assists Nuclear Pharmacists in the Molecular Imaging and Therapy Services (MITS) with the preparation and dispensing of radioactive drugs for cancer patients. The technician responsibilities include following Standard Operating Procedures for the safe preparation and dispensing of radiopharmaceuticals used for Diagnostic, Therapeutic and Research use. Tasks involve performing Quality Control (QC) testing on various drug samples, facility and equipment maintenance & cleaning, radiopharmaceutical package receiving and shipment, performing radiation safety functions, and waste management. The technician is a member of the multidisciplinary team whose skills are fundamental to MITS Pharmacy’s success in supplying safe clinical-grade drugs to our patients. Requirements:At least an Associate’s degree with the following skills/experience:- Required Skills/Experience:- Nuclear Pharmacy Technician experience required (Minimum 1 year)- Candidate must have impeccable communication skills - Candidate must have excellent organizational skills for data and document management- Ability to adapt in a highly dynamic environment - Must be a team player with patient-centric focus - Preferred Skills/Experience:- Pharmacy Compounding of sterile preparations (working knowledge of USP 797 & 825)- PTCB/NPH preferred- Omnicell experience preferred- PET/SPECT Radiopharmaceutical handling experience preferred
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PER DIEM Advanced Practice Provider (Physician Assistant or Nurse Practitioner) - Inpatient Bone Marrow Transplant (BMT) Service (DAYS)Hours: 7 am-7:30 pm shifts Our dedicated team is growing and we are looking to hire an Advanced Practice Provider (Physician Assistant or Nurse Practitioner) to deliver comprehensive care to the inpatient BMT population in order to meet the medical and psychosocial needs of our patients, implement and evaluate standards of care, and participate in research necessary to establish exemplary, evidence-based care. Are you ready to find your calling and make a difference in the lives of our patients and their families?WE ARE: The Advanced Practice Provider (APP) will join a team of over 800 NPs and PAs across MSK who have dedicated their lives to deliver compassionate, comprehensive cancer care to patients and their loved ones, supporting the mission, philosophy, standards, goals and objectives of the institution and department.YOU ARE:- A good decision-maker, known to work at making timely decisions that keep the organization moving forward- Able to work effectively in an environment notable for complex, sometimes contradictory information- Effective at gaining the support and dedication of others by engaging them around your point of view and priorities- Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstancesYOU WILL:- Collaborate with physicians and healthcare team members- Deliver comprehensive care to BMT Oncology patients in an inpatient setting- Meet the medical needs of patients- Participate in the implementation of patient education and clinical support programs to ensure optimal care throughout the healthcare continuumQUALIFICATIONS NEEDED FOR A PA APPLICANTS ARE:- Graduate from an accredited PA program- NCCPA certification- Active NYS license or able to qualify for state licensure- A minimum of 3 years of similar experience is preferredQUALIFICATIONS NEEDED FOR AN NP APPLICANTS ARE:- Current New York State (NYS) RN and NP licenses/registrations- Master’s degree in nursing, prescriptive privileges (or eligibility)- 3+ years of related clinical experience- Related National NP certification
