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Fortrea Hiring | Safety Science Coordinator Bangalore Fortrea (formerly Covance / LabCorp Drug Development) Are you searching for Pharmacovigilance jobs in Bangalore, Fortrea safety science careers, or fresher-friendly drug safety vacancies for B.Pharm and Life Sciences graduates in India Global clinical research organization Fortrea is hiring a Safety Science Coordinator 1 for its Patient Safety Services (PSS) team based in Bangalore, Karnataka. In this key pharmacovigilance role, you will assist with the complete adverse events lifecycle from receiving and logging AE/SAE reports, writing patient narratives and MedDRA coding, to submitting Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs) to clients, Regulatory Authorities, Ethics Committees, and investigators within mandated timelines. This is an excellent opportunity for freshers (BS/BA with 06 months) and experienced candidates (up to 2 years) holding degrees in Pharmacy, Life Sciences, Nursing, or Medical Sciences. To format a recruiterready professional resume highlighting your adverse event processing, MedDRA coding, and safety database skills, read our guide on how to apply for healthcare and pharma jobs online. Job Overview Job Title: Safety Science Coordinator 1 Department: Patient Safety Services (PSS) / Pharmacovigilance Employment Type: Full-Time, Permanent Job Requisition ID: 264333 Application Closing Date: 06 August 2026 Qualifications: B.Sc / B.Pharm / M.Sc / M.Pharm / PharmD / Nursing / Life Sciences Required Experience: Freshers (06 Months) to 2 Years in Safety / PV / Pharma Work Mode: Office / Remote As a Safety Science Coordinator at Fortrea, your major accountabilities will include: AE/SAE Processing & Data Entry: Log incoming Adverse Event (AE) and Serious Adverse Event (SAE) reports into safety tracking databases and forward them per SOPs. MedDRA Coding & Narrative Writing: Write patient safety narratives and accurately code adverse events using MedDRA terminology for clinical and postmarketing products. ESR & PSR Submissions: Process and submit Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs) to clients, Regulatory Authorities, Ethics Committees, and investigators within agreed timelines. Quality Review & Database Reconciliation: Assist with peer/quality review of processed safety reports, identify trends, and support reconciliation of safety databases. SOP Compliance & Mentoring: Work within the Quality Management System (QMS), train and mentor PSS Assistants, and maintain safety study files for archiving. BS/BA in Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or related disciplines with 0 to 6 months of Safety or relevant experience. MS/MA or PharmD with 0 to 6 months of Safety or relevant experience. Associate degree with 6 months to 1 year of Safety or relevant experience. Nondegree holders with 1 to 2 years of handson Safety experience. Understanding of AE/SAE report processing, safety narrative writing, MedDRA coding and regulatory submission workflows. Proficiency in MS Office (Word, Excel) and safety databases. Strong attention to detail, logical reasoning, time management, and the ability to handle multiple projects concurrently. Good written and verbal English communication skills. Resume Tips for Fortrea Safety Science Candidates Highlight AE/SAE Processing & MedDRA Skills: Prominently feature any experience or academic project work in adverse event processing, MedDRA coding, and safety database entry in your executive summary. Detail Regulatory Submission Familiarity: Mention your knowledge of ESR/PSR timelines, CIOMS forms, E2B submissions, and regulatory authority reporting (CDSCO, FDA, EMA). Add Technical Keywords: Optimize your CV with keywords like Safety Science Coordinator, Pharmacovigilance, AE/SAE, MedDRA, ESR, PSR, Patient Safety, Fortrea, and Bangalore. Fortrea Safety Science Coordinator Interview Questions Q1. What is the difference between an Adverse Event (AE) and a Serious Adverse Event (SAE) Answer Guidance: An AE is any untoward medical occurrence in a patient during treatment, regardless of causality. An SAE is an AE that results in death, is lifethreatening, requires hospitalization, causes disability, or is a congenital anomaly requiring expedited reporting to regulators. Q2. What is MedDRA and how is it used in pharmacovigilance case processing Answer Guidance: MedDRA (Medical Dictionary for Regulatory Activities) is a standardized medical terminology used to classify and code AE/SAE terms at five hierarchical levels (SOC, HLGT, HLT, PT, LLT) for consistent regulatory reporting across all safety databases. Q3. What are Expedited Safety Reports (ESRs) and what are the typical submission timelines Answer Guidance: ESRs are urgent regulatory reports for serious, unexpected adverse events. Fatal/lifethreatening SUSARs must be submitted within 7 calendar days (with followup at 15 days), while other