B Pharma & M Pharma Medical Writing Job Vacancy @ Cipla Ltd

B Pharma & M Pharma Medical Writing Job Vacancy @ Cipla Ltd

Cipla ltd hiring pharma candidates. M Pharma job opening 2022. M Pharma job opening 2022. Candidates with master’s degree in pharma may apply for the job opening at Cipla Ltd. Pharma job opening 2022. M Pharma job opening 2022. Check out all the details on the same below:

Job Title: Team Member – Medical Writing

Id: (67798)

Eligbility Criteria: 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. Pharm (Pharmacology), MSc (Clinical research) with at least 2-3 years of experience in medical and regulatory writing PhD (Pharmacology) with at least 1-2 years of experience in medical and regulatory writing

Competencies/Skills

  • Communication Skills (clarity of thought, comprehension)
  • Likely potential for growth
  • Job / Product / Technical Knowledge / Pharma domain knowledge
  • Presentation & Interpersonal skills (If applicable)
  • Managerial or People Management skills
  • Safety awareness (If applicable)
  • Relevance of Previous Experience
  • Comprehension, Analytical & Problem solving abilities
  • Productivity & Result Orientation (If applicable)
  • Attitude
  • Qualification fitment
  • Sales drive (If applicable)
  • Personality traits (Individualistic / Team player, Out spoken, Maturity level etc.)

Division IPD

Department IPD

Employment Type Permanent

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 the regulated and non-regulated markets 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 frameworks 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

Apply Online

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