Senior Specialist - Plainsboro Township
2 weeks ago

Job summary
The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization.
Responsibilities
- Ensures implementation of best possible retention in key clinical trials in US/CA
The retention team works in close collaboration with Medical Directors - Pro-actively drives collaboration with the TM(s) in CDO to obtain/share trial specifics issues relating to titration across all trial sites, concentrating on areas related to quality, site performance and metrics
- Demonstrates technical expertise within responsibility areas, staying up-to-date of new practices and building knowledge of emerging trends and advances within area.
- Maintains responsibility for quality, performance, regulatory compliance and patient safety related to managing assigned clinical trial sites and document handling.
- Sends follow-up emails or communications that do not provide solutions but only confirm if they have read your email.
- Attends and participates in trial team meetings Investigator and Monitor Meetings.
- Collaborate with sites on surveillance plane development after discontinuation.
- Achieve individual patient surveillance by connecting directly with site staff on specific cases.
- This position may require overnight travel up to 10-20%.
to limited creating presentations training site staffJob description
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