Randstand Hiring 30 Drug Safety Trainees – Freshers Pharmacovigilance (₹2.5–4 LPA)

Global Pharma Hiring 30 Drug Safety Trainees in Bangalore – Freshers Welcome (₹2.5–4 LPA)

A leading global pharmaceutical company, through Randstad, is hiring 30 Drug Safety Trainees for its pharmacovigilance operations in Bangalore (Work From Office). This is a full-time entry-level opportunity open to freshers from Life Sciences and Pharmacy backgrounds, with joining scheduled for March 2026. The role offers structured training in drug safety case processing, adverse event management, medical coding, and global pharmacovigilance standards. The salary range for this position is ₹2.5 to ₹4 LPA, based on qualifications and assessment performance.

This opportunity is ideal for candidates who want to build a long-term career in pharmacovigilance, clinical safety, regulatory compliance, and global drug safety operations within a multinational pharmaceutical environment.

---

Company Overview

Randstad is a globally recognized talent solutions organization that partners with leading pharmaceutical, biotechnology, and healthcare companies worldwide. Through strategic hiring partnerships, Randstad supports workforce expansion for regulated drug safety and clinical research operations.

The hiring organization is a global pharmaceutical company with established pharmacovigilance systems aligned with international regulatory standards including FDA, EMA, ICH, and global safety reporting guidelines. The company operates structured drug safety databases, validated workflows, and compliance-driven case processing systems to ensure patient safety and regulatory adherence.

Working in such an environment provides early-career professionals exposure to global safety reporting standards, multinational regulatory frameworks, and structured career progression within the pharmacovigilance domain.

---

Job Role & Responsibilities

As a Drug Safety Trainee, you will undergo structured training and gradually handle safety case processing activities under supervision. The role focuses on individual case safety report (ICSR) management and compliance with global pharmacovigilance regulations.

ICSR Processing

• Perform data entry and processing of Individual Case Safety Reports (ICSRs)
• Review source documents for completeness and accuracy
• Ensure case processing timelines are met as per global regulatory requirements

Adverse Event (AE) & Serious Adverse Event (SAE) Handling

• Identify and document adverse events from various sources
• Classify seriousness and expectedness as per safety guidelines
• Escalate critical cases as required under supervision

Medical Coding

• Perform coding using MedDRA terminology for adverse events
• Use WHO-DD for product coding and drug dictionary alignment
• Ensure standardized terminology usage across safety databases

PV Documentation & Compliance

• Maintain accurate pharmacovigilance documentation
• Support preparation of regulatory safety reports where required
• Ensure adherence to Good Pharmacovigilance Practices (GVP)
• Follow internal SOPs and global drug safety standards

Learning & Development

• Participate in training sessions on global safety databases
• Understand regulatory reporting timelines for FDA, EMA, and other agencies
• Gain exposure to audit readiness and compliance procedures

This role builds strong foundational expertise in global pharmacovigilance operations and prepares candidates for advanced roles such as Drug Safety Associate, PV Specialist, or Safety Reviewer.

---

Eligibility / Qualifications

This opportunity is specifically designed for fresh graduates seeking entry into the drug safety domain.

Educational Qualifications

B.Pharm, M.Pharm, PharmD, B.Sc Life Sciences, M.Sc Life Sciences

Relevant disciplines may include:

Pharmacology, Pharmaceutical Sciences, Clinical Research, Biotechnology, Microbiology, Biochemistry

Experience Requirement

• Freshers are eligible to apply
• Basic understanding of pharmacovigilance concepts is an added advantage

Required Skills

• Strong attention to detail
• Good analytical ability
• Basic knowledge of medical terminology
• Good written and verbal communication skills
• Willingness to work in a structured office environment

---

Location & Salary

Job Role: Drug Safety Trainee
Location: Bangalore (Work From Office)
Joining: March 2026
Open Positions: 30
Salary: ₹2.5 – ₹4 LPA

Compensation will be offered based on qualification, assessment results, and company standards. This role provides structured training and strong career growth potential in global pharmacovigilance operations.

---

Application Process

Interested and eligible candidates can apply by sending their updated CV to the email below:

Email: sahana.s@randstad.in

Candidates are advised to mention “Drug Safety Trainee – Bangalore” in the subject line while applying. As there are only 30 openings, early application is strongly recommended.

---

Frequently Asked Questions (FAQs)

Who can apply for this Drug Safety Trainee position?
Fresh graduates from Pharmacy and Life Sciences backgrounds are eligible.

Is prior pharmacovigilance experience required?
No. This is a fresher-level opportunity with structured training.

What skills will I learn in this role?
You will learn ICSR processing, AE/SAE handling, MedDRA coding, PV documentation, and global drug safety compliance.

Is this a remote job?
No. This is a work-from-office role based in Bangalore.

How many vacancies are available?
There are 30 open positions.

---

Summary Table

Company	Global Pharma Company (via Randstad)
Vacancies	Drug Safety Trainee (30 Positions)
Required Education	B.Pharm, M.Pharm, PharmD, B.Sc, M.Sc Life Sciences
Experience	Fresher

Tagged as: Pharma Jobs in Bangalore