06 Aug
|
Indegene
|
Bengaluru
06 Aug
Indegene
Bengaluru
We are seeking a candidate with expertise in core authoring of various clinical document types that support regulatory filings. Preference will be given to those with experience in Module 2.4, 2.5, 2.6, 2.7, and 5.2, as well as clinical study reports (CSRs), protocols, amendments, informed consent forms (ICFs) and amendments, and Investigator Brochures (IBs).
Location: Bangalore, Hyderabad, Pune, Mumbai, Delhi
Work Model: Hybrid
Education: MBBS/PhD/MDS/BDS/MPharm/PharmD
Experience: 10 to 12 years in writing Clinical & Regulatory documents supporting global filings (CTD Module 2 and Module 5)
Team Handling Experience: Required
📌 Associate Manager (Bengaluru)
🏢 Indegene
📍 Bengaluru