Lead - Regulatory Writing

Indegene India
Posted 1 month, 3 weeks ago

Job Description

Education: MBBS/PhD/MDS/BDS/MPharm/PharmD Experience: 6-10 years in writing Clinical & Regulatory documents for global filings (CSR, CSP, CTD Module 2, and Module 5) Role Purpose: The Lead Medical Writer will develop and review medical writing deliverables that support the clinical regulatory writing portfolio and provide training to junior writers. Skills Required: - Experience in authoring various clinical document types for regulatory filings, with a preference for Module 2.4, 2.5, 2.7, 5.2,…

Requirements

Employment Type

Permanent

Category

Scientific & QA Jobs

About Indegene

Location: India

Industry: Scientific & QA Jobs

Sign in to apply or see your match score

Sign In to Apply Create Account
Quick Actions
Back to Job Search

Leaving careerAIForge

Lead - Regulatory Writing

Indegene

You will be redirected to an external website to complete your application.
What happens next:
• You'll be taken to the employer's application page
• Complete the application on their website
• We'll track that you applied for your records