MSK, dar žinoma kaip „Multi Services Kent“, yra Jungtinėje Karalystėje veikianti objektų aptarnavimo įmonė, padedanti įgyvendinti statybos projektus ir turinti daugiau kaip 20 metų patirties. Įmonės veikla apima objektų logistiką, demontavimo ir parengimo darbus, apsaugą, saugumą ir patekimo kontrolę, atliekų tvarkymą ir perdirbimą, geležinkelių sektoriaus konsolidavimo paslaugas, įrenginius ir įrankius bei pasirengimą statybai. Įmonė praktinį objektų koordinavimą derina su dėmesiu saugai, tvarumui ir socialinei vertei.
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.
Aprašymas
- 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
Reikalavimai
- 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