MSK jeb Multi Services Kent ir Apvienotajā Karalistē bāzēts būvobjektu pakalpojumu uzņēmums, kas atbalsta būvniecības projektus un kam ir vairāk nekā 20 gadu pieredze. Uzņēmuma darbība ietver objektu loģistiku, demontāžu un sagatavošanu, aizsardzību, drošību un piekļuves kontroli, atkritumu apsaimniekošanu un pārstrādi, dzelzceļa nozares konsolidācijas pakalpojumus, tehniku un instrumentus, kā arī atbalstu pirms būvniecības. Uzņēmums apvieno praktisku objektu koordinēšanu ar koncentrēšanos uz drošību, ilgtspēju un sociālo vērtību.
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.
Apraksts
- 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
Prasības
- 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