Posted:2 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • Planning, conducting, supervising and reporting of BA/BE studies in accordance with Protocol, ICH-GCP guideline and regulatory requirements.
  • Coordination with external service providers and cross-functional teams
  • Data submission of clinical studies as per requirement to Pharmacovigilance and RA department.
  • Regulatory inspection compliance
  • SOP preparation, review, revalidation, and training to all team members.
  • Plan Calender training. External training such as ACLS BLS, GCP. Mock drills , internal trainings and seminars.

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Cadila Pharmaceuticals Limited logo
Cadila Pharmaceuticals Limited

Pharmaceuticals

Ahmedabad

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