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Are you seeking an opportunity to be at the forefront of innovation during this exciting time at Memorial Sloan Kettering Cancer Center? This is a great role for someone who has the right skills, who wants to be part of a dynamic team and who wants to learn how to apply their skills to support our mission: the progressive control and cure of cancer through programs of patient care, research, and education.https://youtu.be/9R7QoNfmm0w We have an exciting opportunity in our Infectious Disease service as a Clinical Research Associate. As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Associate (CRA) coordinates and maintains the assigned research portfolio for a Service and/or Department.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.You are:- Adept at anticipating and prioritizing work to meet commitments of multiple stakeholders.- Adept at building partnerships and working collaboratively to influence others to meet shared objectives and goals.- Known as someone who improves processes and proactively, independently identifies solutions that anticipate stakeholder needs.You have:- HS Diploma/GED with 2-4 years relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory, OR Bachelor’s Degree with at least 1 full year of relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory.- Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications required.- Proficiency with the Electronic Medical Record (EMR) system.- Excellent computer skills, including proficiency in Microsoft Office Products and other software programs for database management/queries, generating reports and developing graphics.- Knowledge of clinical research data collection processes in accordance with GCP.
The Advanced Light Microscopy Operation of the Molecular Cytology Core Facility at MSK is seeking a Senior Research Scientist/Senior Microscopy Specialist to join their team. The Molecular Cytology Core Facility is offering a full-time position for a highly motivated person who is interested to apply and further develop his skills to support scientists and students with image acquisition and data analysis. The MCCF is supporting complex microscopy setups, including Zeiss confocal/Airyscan, Leica confocal microscopes (SP5 on an upright stand, SP5 on an inverted stand and SP8/WLL&APDs), widefield bright field/fluorescence microscopes, laser capture microdissection microscope, digital slide scanners and image analysis workstations with a range of software packages, e.g. Imaris, AutoQuant, MatLab, FIJI/ImageJ, Voloom, CaseViewer. We have more than hundred users with a diverse range of applications and imaging needs. The new team member is expected to work with image processing and image analysis in the dynamic environment of basic and clinical researchers, as well as oversee the training of the scientists, using the equipment. As the Senior Research Scientist/Microscopy Specialist You Will: - maintenance of the daily operation of the high-end light microscopes and equipment infrastructure, including instrument performance tests, troubleshooting, alignments- teaching microscopy classes- writing reports, preparing presentations, collaborating in scientific papers- user consultation, training and assistance with routine and advanced light microscopy techniques to ensure correct set up and optimum microscope operation- provide project-based advice for preparation of biological samples, including fixation, tissue sectioning, tissue clearing and expansion microscopy, image acquisition, data processing and image analysis- maintenance and upgrades of the Core infrastructure (network, computers, servers, software) in coordination with the IT team You Need: - PhD in (Biology, BioPhysics or related fields with several years of work experience with microscopy image processing and image analysisS- Strong service and team-orientation, and excellent organizational, problem-solving and communication skills- Practical experience with data processing, data management, image analysis, programming and advanced imaging techniques- A passion for learning and problem solving- Strong organizational skills, flexibility in working hours and ability to multi-taskInterested candidates should complete the online application and include a CV, cover letter that includes a list of relevant experience and the names of three references.
Do you want to be a part of something bigger than yourself? At Memorial Sloan Kettering Cancer Center, 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 looking for Clinical Research Coordinators (CRC) to join as an integral member of a research team. In this role, and in compliance with all regulatory, institutional, and departmental requirements, you will have ownership of maintenance of data management on clinical studies. If you're looking to expand your horizons and explore your interests in healthcare and medicine, submit your application today.You 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- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding- Resilient in recovering from setbacks and skilled at finding detours around obstacles- Passionate about medical terminology and science- You are familiar with and excited about working with and organizing large amounts of dataYou Will:- Collect, abstract, and enter data for research projects, databases and/or protocols (clinical trial) including reviewing patient charts, existing databases, and other sources within a specified timeframe- Ensure data quality and integrity throughout the life of the study.- Collaborate with team members and individuals across MSK regarding data input- Generate data reports and deliver to all necessary parties on the progress of research project, database or protocol- Ensure that we are following all appropriate Institutional, State, and Federal regulations throughout the study, and complete all regulatory documentation to ensure that research protocols are approved by Institutional Review Board- Provide clerical and administrative support, such as filing and scheduling meetings and appointments as neededYou Have:- A Bachelor’s degree OR a high school diploma and 2 years of research experience- The ability to commit to at least 2 years- 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