Pharmacovigilance Apprentice Opportunity | Drug Safety Role at Fortrea

Fortrea Hiring Apprentice Drug Safety | MSc Life Sciences Freshers | Bangalore

Fortrea is hiring an Apprentice – Drug Safety for its Pharmacovigilance department in Bangalore, India. This is a full-time, office-based opportunity designed for fresh postgraduates in Life Sciences who want to build a career in pharmacovigilance, adverse event reporting, clinical trial safety, and global drug safety operations.

Candidates with 0–1 year of experience in drug safety or strong exposure to clinical trials during academics are eligible to apply. This entry-level pharmacovigilance role provides structured exposure to safety case processing, SAE/SUSAR reporting, MedDRA coding, periodic safety reports, and regulatory compliance within a global clinical research environment.

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Company Overview

entity[“organization”,”Fortrea”,”contract research organization”] is a leading global contract research organization (CRO) providing clinical development, pharmacovigilance, and regulatory services to pharmaceutical, biotechnology, and medical device companies worldwide. The organization supports sponsors across the full clinical development lifecycle, ensuring regulatory compliance, safety surveillance, and data integrity.

With a strong global presence, Fortrea works with leading biopharma innovators to accelerate the development of safe and effective therapies. Its pharmacovigilance and drug safety teams play a critical role in adverse event management, signal detection, regulatory reporting, and risk management across multiple therapeutic areas.

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Job Role & Responsibilities

The Apprentice – Drug Safety will support entry-level pharmacovigilance functions in accordance with Fortrea and sponsor Standard Operating Procedures (SOPs). This role focuses on safety data entry, case processing, coding, regulatory reporting support, and compliance documentation.

Adverse Event Case Processing

• Perform data entry of safety data into adverse event tracking systems.
• Write clear and medically accurate patient narratives.
• Code adverse events using MedDRA and WHO Drug Dictionary (WHODD) for marketed products where applicable.
• Assist in listedness assessment against approved product labels.
• Support causality assessment activities in collaboration with medical staff.
• Generate queries and collect missing or discrepant information as needed.

Regulatory Reporting & Compliance

• Assist in submission of expedited SAE and SUSAR reports to clients, regulatory authorities, ethics committees, investigators, vendors, and internal stakeholders within defined timelines.
• Support preparation, review, and approval of Periodic Safety Reports (PSRs) for investigational products and medical devices.
• Ensure compliance with global pharmacovigilance regulations, GCP guidelines, and safety reporting timelines.

Collaboration & Quality Standards

• Work closely with internal teams and external stakeholders to ensure case completeness and regulatory accuracy.
• Maintain documentation aligned with sponsor and company quality standards.
• Participate in departmental activities and support process improvements where required.

This position requires strong attention to detail, structured documentation skills, and the ability to manage multiple safety cases within regulatory timelines.

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Eligibility & Qualifications

Educational Qualification

Candidates must have completed a Master’s degree in Life Sciences or related disciplines such as:
MSc Pharmacology, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Clinical Research, MSc Life Sciences, MSc Biomedical Sciences, M.Pharm, PharmD.

Experience

• 0–1 year of experience in Drug Safety or Pharmacovigilance.
• Strong exposure to clinical trials during academic training is preferred.

Required Skills

• Basic understanding of pharmacovigilance regulations and safety reporting processes.
• Knowledge of MedDRA and WHO Drug Dictionary coding concepts.
• Strong written and verbal communication skills.
• Ability to manage multiple tasks and meet strict timelines.
• Collaborative mindset with ability to work across diverse teams.
• High level of accuracy and compliance awareness.

Fresh postgraduates with strong academic performance and interest in clinical research safety are encouraged to apply.

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Location & Employment Details

• Location: Bangalore, India
• Work Mode: Office-Based
• Employment Type: Full-Time
• Experience Level: Entry-Level (Apprentice)
• Job Requisition ID: 26542
• Application Deadline: February 25, 2026

Fortrea offers structured onboarding, exposure to global pharmacovigilance systems, and opportunities for career growth within clinical research and drug safety operations.

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Application Process

Interested candidates can apply directly through Fortrea’s official career portal using the link below:

Apply Here: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Bangalore/Apprentice-Drug-Safety_26542?source=LinkedIn

Applicants should highlight their academic research, clinical trial exposure, safety reporting knowledge, and familiarity with pharmacovigilance concepts in their resume.

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Career Growth Opportunities

With experience, professionals can progress into roles such as:

• Drug Safety Associate
• Pharmacovigilance Executive
• Safety Data Specialist
• Clinical Safety Scientist
• Regulatory Safety Officer

The pharmacovigilance sector continues to expand globally, driven by increasing regulatory oversight and post-marketing surveillance requirements.

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Frequently Asked Questions (FAQs)

1. Is this role open to freshers?

Yes, fresh postgraduates with 0–1 year of experience are eligible.

2. Is prior pharmacovigilance experience mandatory?

No, but strong academic exposure to clinical trials and safety concepts is preferred.

3. What coding dictionaries are used?

MedDRA and WHO Drug Dictionary (WHODD) are used for coding adverse events and products.

4. Is this a remote position?

No, this is an office-based role in Bangalore.

5. Does the role involve regulatory reporting?

Yes, the role includes assisting with expedited safety reports and periodic safety documentation.

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Summary Table

Company	Fortrea
Vacancies	Apprentice – Drug Safety
Required Education	MSc Life Sciences, MSc Pharmacology, Biotechnology, Microbiology, Biochemistry, M.Pharm, PharmD
Experience	0–1 year Drug Safety experience; strong clinical trial exposure preferred