MSK, also known as Multi Services Kent, is a UK-based site services company supporting construction projects with more than 20 years of experience. Its work spans site logistics, strip-out and set-up, protection, security and access control, waste management and recycling, rail consolidation, plant and tools, and pre-construction support. The company’s approach brings together practical site coordination with a focus on safety, sustainability, and social value.
Research Regulatory Associate, Early Drug Development
Coordinate regulatory records and compliance for clinical trials at MSK. Work with investigators, sponsors, and research teams in New York City.
United States
New York$69,400 – $107,600 / year
HybridFull-timeJuniorMiddleNo degree requiredEnglish RequiredComplianceDescription
- Coordinate regulatory tasks and trial records across multiple principal investigators and research teams
- Keep regulatory files current and ready for audits
- Ensure studies follow protocols and policies
- Suggest practical ideas and solutions to support team effectiveness
- Share study progress with internal and external partners
- Spot study trends and develop and implement responses
- Own key tasks while building skills and knowledge
- Act as the main contact for external sponsors and CROs
- Attend and sometimes lead weekly protocol meetings
- Create, update, and maintain protocol tools that support accurate clinical research
- Report to the Research Project Manager
Requirements
- At least two years of clinical research or regulatory experience
- Knowledge of regulations governing human subject protection and HIPAA
- Strong attention to detail and analytical ability
- Able to work independently and advance a high volume of work
- Strong planning and prioritization skills
- Critical thinking and problem-solving skills
- Excellent communication skills and confidence interacting professionally across all levels
- Enthusiasm for and commitment to MSK’s vision, mission, and values