Study Inspection Manager
Cpl Life Sciences US New Jersey, United States (Hybrid)
Exciting Opportunity at an established biotechnology company!
Are you passionate about advancing groundbreaking therapies in biotechnology? a leading innovator renowned for developing transformative medications in the biotechnology space is expanding its clinical team!
We're seeking a proactive individual to join our client on a 12-month contract, as a Study Inspections Manager who will oversee activities to ensure inspection readiness, supporting the Program Operations Leader and Clinical Study Lead for one or more clinical programs within Clinical Trial Management.
Requirements:
- 8 years of relevant industry experience
- Hybrid role
- Experience with global agency inspections.
- Deep expertise in R&D, including global clinical trial operations and the creation of protocols and key study documents.
- Proficient in trial management systems, MS Office applications, including IVRS/IWRS, and EDC.
Seniority Level: Mid/Senior Level
Industry: Biotechnology Research
Employment Type: Contract
Job Functions: Accounting/Auditing