CIPLA Career Opportunities: Team Member - Medical Writing B. Pharm/ M. Pharm/ PhD Apply Now
Job Purpose
Develop and review clinical documents for regulated
and non-regulated markets ensuring regulatory compliance and thus assisting
on-time product registration and renewal
Accountabilities
1. Develop and review documents for clinical and
bioequivalence studies to align with product strategy and registration
2. Develop and review common technical documents for
regulated and non-regulated market as per country specific guidance for timely
registration and renewal of dossier
3. Prepare proposals and justification of queries to
different regulatory bodies by gathering literature to obtain approvals/waivers
for the molecule
4. Prepare and review SOPs and templates to implement
standardized systems and document framework to achieve consistent quality and
uniformity in documentation
5. Prepare manuscripts/ abstracts for publication by
evaluating the studies conducted by Cipla to represent Cipla globally
Education Qualification
B. Pharm/ M. Pharm/ PhD (Pharmacology)/MSc (Clinical
research)
Relevant Work Experience
B. Pharm with at least 3-4 years of experience in
medical and regulatory writing or M. Pharm (Pharmacology), MSc (Clinical
research) with at least 2-3 years of experience in medical and regulatory
writing or PhD (Pharmacology) with at least 1-2 years of experience in medical
and regulatory writing
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