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PHARMA JOBS POST > Pharma Jobs > Fortrea Jobs 2026: Safety Science Coordinator I Vacancy in Pune (0–1 Year Experience)
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Fortrea Jobs 2026: Safety Science Coordinator I Vacancy in Pune (0–1 Year Experience)

ADMIN
Last updated: April 10, 2026 3:19 pm
ADMIN 1 month ago
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Fortrea Hiring Safety Science Coordinator I in Pune

Fortrea is hiring for the position of Safety Science Coordinator I at its Pune location. This is an excellent opportunity for freshers and candidates with up to 1 year of experience in pharmacovigilance or clinical safety.

Contents
Fortrea Hiring Safety Science Coordinator I in Pune📍 Job DetailsKey Responsibilities🔹 Safety Reporting & Case Processing🔹 Regulatory & Compliance🔹 Data Management & Quality🔹 Coordination & Support🎓 Eligibility Criteria✔️ Educational Qualification✔️ ExperienceRequired SkillsWhy Join Fortrea?📌 How to ApplyAPPLY HERE

The role focuses on handling adverse event (AE/SAE) processing, safety reporting, and regulatory compliance within clinical trials and post-marketing environments.


📍 Job Details

  • Position: Safety Science Coordinator I
  • Location: Pune, India
  • Job Type: Full-Time
  • Job ID: 26879
  • Last Date to Apply: April 11, 2026 (Apply ASAP – limited time left)

Key Responsibilities

🔹 Safety Reporting & Case Processing

  • Process Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs)
  • Perform data entry of AE/SAE cases into safety databases
  • Write patient narratives and perform MedDRA coding
  • Handle listedness assessment for marketed products

🔹 Regulatory & Compliance

  • Submit SAE reports to regulatory authorities, clients, and ethics committees
  • Ensure compliance with global safety regulations and timelines
  • Maintain safety documentation and tracking systems

🔹 Data Management & Quality

  • Maintain and update adverse event tracking systems
  • Perform quality review and reconciliation of safety databases
  • Generate queries for missing or inconsistent data

🔹 Coordination & Support

  • Support project teams and safety personnel
  • Schedule meetings and maintain project documentation
  • Train and mentor junior team members
  • Assist in archiving safety study files

🎓 Eligibility Criteria

✔️ Educational Qualification

Candidates from the following backgrounds are eligible:

  • B.Pharm / M.Pharm / PharmD
  • Life Sciences / Biological Sciences / Nursing / Medical Sciences

✔️ Experience

  • Freshers to 1 year of experience in:
    • Pharmacovigilance (PV)
    • Clinical Safety
    • Regulatory Affairs / Clinical Data Management

Required Skills

  • Strong attention to detail
  • Good written & verbal communication
  • Basic knowledge of MS Office & data handling
  • Ability to manage multiple tasks
  • Team player with problem-solving skills

Why Join Fortrea?

  • Work with a leading global CRO organization
  • Exposure to clinical trials & pharmacovigilance
  • Career growth in drug safety & regulatory domain
  • Opportunity to work on international projects

📌 How to Apply

Interested candidates can apply directly through the official Fortrea careers portal using Job ID 26879.

👉 Apply immediately as the deadline is very close!

APPLY HERE

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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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