Full-time
Research Regulatory Associate, Early Drug Development
$69K/yr – $108K/yr
Comprehensive cancer care, research, and training centerScience & PharmaceuticalPosted 21d ago
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Role overview
Job type
Salary
$69K/yr – $108K/yr
Sector
Posted
21 days ago
Job description
Responsibilities
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
Benefits
Hybrid schedule
Glassdoor
3.8
Comprehensive cancer care, research, and training center.
New York, New York, USA
http://www.mskcc.org
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Legal and Compliance
Engineering and Development
Customer Service and Support
Management and Executive
Education and Training
Accounting and Finance
Product Management
Creatives and Design
Public Sector and Government
Human Resources
Arts and Entertainment
Sales
Trends of Total Sponsorships
*2026
(159)
2025
(258)
2024
(284)
2023
(282)
2022
Qualifications
2 years of Clinical Research/Regulatory experience
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
2 years of Clinical Research/Regulatory experience.
Required skills
Clinical Research, Regulatory Affairs, Human Subject Protection Regulations, HIPAA
Experience
2+ years
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