Full Time, Permanent
Mumbai (All Areas)
10-15 years
Designing BE protocols, CSR reviews, monitoring, query handling, coordination activities related to BE studies, and clinical trials/PK studies for biosimilars and complex generics.
Skills
Clinical Research
Bioavailability Bioequivalence
Pharma
BA / BE
Pharmacovigilance
Clinical Trials
Responsibilities
- Designing BE protocols
- CSR reviews
- Monitoring
- Query handling
- Coordination activities related to BE studies
- Clinical trials/PK studies for biosimilars and complex generics
Job Information
- Role: Clinical research Scientist
- Industry Type: Pharmaceutical & Life Sciences
- Department: Research & Development
- Role Category: Pharmaceutical & Biotechnology
Education
- UG: B.Pharma in any specialization
- PG: M.Pharma in any specialization
Qualifications
- Applicant must be having 10+ years of experience in handling Bioavailability/Bioequivalence (BA/BE) studies
- Strong understanding of current BA/BE guidelines (USFDA, EMA, Health Canada, WHO, etc.)
How to apply
Submit your resume to info@finejobs.in