0 years
0 Lacs
Posted:2 weeks ago|
Platform:
On-site
Full Time
Primary Responsibilities Medical monitoring of the in-house clinical trials and overseeing of CRO medical monitoring of outsourced projects Development and review clinical documents including protocol, investigator's brochure, case record form, product rationale, prescribing information, drug interactions etc Organization of Subject Expert Committee meeting materials and attending SEC meetings for clinical trials and marketing approvals Secondary Responsibilities Medical Review of ICSRs, Aggregate reports, Signal reports and Risk Management plans Review of clinical and non-clinical overviews and summaries of CTD Review of medical rationale for CT waiver applications New products evaluation for development Develop, review and approve marketing requests of product evaluations, comparative safety and efficacy training material Mentoring/ training team members to gain required skills to enable on-time deliverables. Show more Show less
Hetero
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Hyderabad / Secunderabad, Telangana, Telangana, India
0.5 - 0.5 Lacs P.A.
Hyderabad, Telangana, India
Experience: Not specified
Salary: Not disclosed
Hyderabad, Telangana, India
Experience: Not specified
Salary: Not disclosed