Fortrea Hiring Freshers for Apprentice – Drug Safety (Pharmacovigilance): Apply Now
Fortrea is inviting applications for the role of Apprentice – Drug Safety at its Bangalore office. This opportunity is ideal for fresh postgraduates from Life Sciences who are looking to launch their career in pharmacovigilance, drug safety operations, and clinical trial safety reporting.
The Apprentice role provides hands‑on training in key areas such as adverse event case processing, MedDRA coding, Serious Adverse Event (SAE) documentation, and periodic safety reporting. Candidates will gain structured exposure to global regulatory requirements and sponsor‑specific SOPs, making it a strong foundation for a long‑term career in drug safety and clinical research.
Job Overview
- Position: Apprentice – Drug Safety (Pharmacovigilance)
- Department: Pharmacovigilance
- Location: Bangalore (Office Based)
- Experience: 0–1 Year
- Qualification: Master’s Degree in Life Sciences
- Job Type: Full-Time
- Application Deadline: 25 February 2026
About the Hiring Organization
Fortrea is a global Clinical Research Organization (CRO) known for its strong expertise in pharmacovigilance (PV) and drug safety operations. With over three decades of clinical research experience, the company supports life sciences organizations in managing clinical trials and ensuring the safety of investigational and marketed products. Fortrea has been recognized as a leader in pharmacovigilance operations, consistently improving safety processes through scientific rigor and innovation
Key Responsibilities
In this role, the Apprentice will support and perform entry‑level pharmacovigilance activities in alignment with Fortrea and/or sponsor Standard Operating Procedures (SOPs). The position provides hands‑on exposure to global drug safety processes and regulatory requirements.
Primary Responsibilities:
- Enter safety information into adverse event tracking systems with accuracy and completeness.
- Draft patient narratives and code adverse events using MedDRA; perform WHODD coding for marketed products when applicable.
- Support listedness assessment by comparing case details against the appropriate product label (for marketed products, as required).
- Assist with causality assessments, working in collaboration with trained medical reviewers.
- Generate queries and help collect missing or inconsistent data by coordinating with medical staff, investigators, or relevant stakeholders.
- Participate in submission of expedited reports such as SAEs/SUSARs to clients, regulatory authorities, ethics committees, investigators, third‑party vendors, partners, and internal Fortrea teams—ensuring all submissions meet required timelines.
- Assist in preparing, reviewing, and supporting approval of Periodic Safety Reports (PSRs) for investigational products or devices, following applicable global regulations and industry guidelines.
Education, Qualifications & Skills
- Minimum educational requirement: Completion of education equivalent to GCSE level or higher, demonstrating strong foundational academic abilities.
- Preferred qualification: A Master’s degree in Life Sciences, such as Biotechnology, Microbiology, Pharmacology, Biochemistry, or related disciplines.
- Project experience: Exposure to delivering and managing multiple academic or professional projects, showcasing the ability to meet deadlines and handle responsibilities effectively.
- Collaboration skills: Ability to work efficiently with cross‑functional stakeholders, including internal teams and external partners, while maintaining clear and professional communication.
- Teamwork & diversity mindset: Shows openness to diverse perspectives and values collaborative problem‑solving through teamwork, partnership, and inclusive thinking.
Salary (Estimated)
- ₹2.8 LPA – ₹4.2 LPA (CTC)
(Based on entry-level drug safety roles in Bangalore market standards)
How to Apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
FAQ
1. What is the role of an Apprentice in Drug Safety at Fortrea?
The Apprentice supports entry‑level pharmacovigilance activities such as adverse event data entry, case processing, narrative writing, MedDRA coding, and assisting with regulatory submissions under the guidance of trained safety professionals.
2. Is this position suitable for freshers?
Yes. This role is specifically designed for fresh postgraduates in Life Sciences who want to start their career in pharmacovigilance and drug safety operations.
3. What educational qualifications are required?
Candidates should have basic schooling equivalent to GCSE level and must have completed a Master’s degree in Life Sciences such as Pharmacology, Biotechnology, Microbiology, Biochemistry, or related fields.
4. Do I need prior experience in pharmacovigilance?
Prior PV experience is not mandatory. However, any exposure to academic or professional projects is an added advantage and demonstrates the ability to handle responsibilities.
