Job Summary
A company is looking for an IRT Sr Project Manager / Associate Director located in Cambridge, MA.
Key Responsibilities:
- Advises on clinical study protocol development focusing on study drug management and IRT operational optimization
- Leads cross-functional efforts for the set-up and maintenance of the IRT System for assigned studies
- Collaborates with various teams to ensure compliance and optimal supply strategies for study medication
Qualifications:
- Bachelor's Degree or equivalent; higher degree preferred
- 6-8 years of experience for Sr. Manager; minimum 8 years for Associate Director
- Profound knowledge in clinical study management and setting up Interactive Response (IRT) Systems
- Strong understanding of GCP and GMP regulations
- Excellent project management skills
Comments