2 years of Clinical Research/Regulatory experience.
Knowledge of human subject protection regulations and HIPAA.
Outstanding attention to detail and strong analytical skills.
Strong planning and prioritizing skills.
Critical thinking and problem-solving abilities.
Excellent communication skills across all levels.
Enthusiasm for MSK's vision, mission, and values.
Responsibilities
Manage regulatory tasks and documentation for clinical trials.
Ensure audit readiness by maintaining up-to-date documents and compliance.
Proactively identify opportunities for team success with innovative ideas.
Communicate study progress to internal and external partners.
Take ownership of key tasks while developing new skills.
Serve as the primary contact for external Sponsors/CROs and lead protocol meetings.
Develop and maintain accurate protocol tools for clinical research.
Benefits
Hybrid work schedule.
Opportunity to contribute to high-impact work in clinical research.
Engagement in meaningful projects that shape the future of medicine.
Supportive team environment focused on collaboration and compassion.
Full Job Description
Exciting opportunity at MSK: Join our Early Drug Development team as a Research Regulatory Associate!
This position offers the opportunity to be part of meaningful, high-impact work where precision, compassion, and collaboration come together. Clinical research staff ensure that research is conducted ethically, efficiently, and with the patient at the center, supporting innovations that shape the future of medicine.
Role Overview:
Manage all regulatory tasks and documentation for clinical trials across multiple Principal Investigators and research study teams.
Ensure MSK is always audit-ready by maintaining up-to-date documents, regulatory files, and ensuring protocol and policy compliance.
Proactively identify opportunities to contribute to the team's success, bringing innovative ideas and solutions to the table.
Effectively communicate the overall study progress to various internal and/or external partners, identify study trends, and build/implement solutions.
Take ownership of key tasks while developing new skills and expanding knowledge.
Primary point of contact for external Sponsors/CROs and participate and/or lead weekly protocol meetings.
Ensure the accurate conduct of clinical research by developing, revising, and maintaining accurate protocol tools at all times.
Key Qualifications:
2 years of Clinical Research/Regulatory experience.
Core Skills:
Knowledge and understanding of regulations pertaining to human subject protection and the Health Insurance Portability and Accountability Act (HIPAA).
Outstanding attention to detail and strong analytical skills; capacity to operate autonomously and drive a high volume of work forward.
Strong planning and prioritizing skills to meet commitments aligned with organizational goals.
Critical thinking and problem-solving abilities to ensure unforeseen issues are handled appropriately and resolved in a timely fashion.
Excellent communication skills and the ability to interact across all levels in a confident, professional manner.
Enthusiasm and dedication to MSK's vision, mission, and values.
Additional Information:
Location: NYC
Schedule: Hybrid
Reporting to the Research Project Manager
Helpful Links:
Compensation Philosophy
Benefits
Pay Range: $69,400.00 - $107,600.00
FSLA Status: Exempt
About Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center is a world-renowned cancer treatment and research institution located in New York City. The center was founded in 1884 and has since become one of the leading cancer centers in the world, with a focus on patient care, research, and education. Memorial Sloan Kettering Cancer Center employs over 20,000 people, including doctors, nurses, researchers, and support staff, and treats over 500,000 patients each year. The center is known for its innovative treatments and cutting-edge research, which has helped to improve the lives of cancer patients around the world. Memorial Sloan Kettering Cancer Center is committed to finding a cure for cancer and improving the quality of life for cancer patients everywhere.
