MSK, znan tudi kot Multi Services Kent, je v Združenem kraljestvu s sedežem podjetje za storitve na gradbiščih, ki podpira gradbene projekte in ima več kot 20 let izkušenj. Njegovo delo obsega logistiko na gradbišču, odstranjevanje in ureditev prostorov, zaščito, varovanje in nadzor dostopa, ravnanje z odpadki in recikliranje, konsolidacijo železniškega transporta, opremo in orodje ter podporo pred začetkom gradnje. Podjetje združuje praktično usklajevanje na gradbišču s poudarkom na varnosti, trajnosti in družbeni vrednosti.
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.
Opis
- 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
Zahteve
- 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