Offer summary
Qualifications:
Advanced degree in Sciences (PharmD, PhD, RN) preferred, 2 years experience as a CRS in the pharmaceutical industry.Key responsabilities:
- Contribute to clinical trial design, analysis, and reporting
- Review scientific data, collaborate cross-functionally, support drug development processes
- Attend congresses, develop program strategy, engage with opinion leaders
- Ensure adherence to GCP, pharmacovigilance standards, regulatory requirements