Fortrea Hiring Fresher Pharmacovigilance – Safety Science Analyst

Fortrea Hiring Safety Science Analyst – Pharmacovigilance Fresher Opportunity in Pune

Fortrea is currently hiring for the position of Safety Science Analyst in Pune, India. This is a 6‑month contract role within the Clinical Safety / Pharmacovigilance department, designed primarily for healthcare and life sciences graduates who want to begin their careers in drug safety and pharmacovigilance operations. The opportunity is open to candidates with 0–1 year of safety experience, making it suitable for freshers and early‑career professionals interested in clinical safety, adverse event reporting, and global pharmacovigilance processes.

The Safety Science Analyst will assist in handling safety data collected from clinical trials and post‑marketing surveillance programs, ensuring accurate processing of adverse events and compliance with regulatory reporting timelines. This role provides exposure to global safety databases, regulatory guidelines, and the end‑to‑end pharmacovigilance workflow used in modern pharmaceutical development.

Professionals selected for this role will collaborate with global clinical safety teams, regulatory specialists, and pharmacovigilance experts to ensure patient safety information is processed accurately and efficiently. For candidates aiming to build careers in drug safety, clinical research, pharmacovigilance operations, and regulatory compliance, this role provides an excellent entry point into the pharmaceutical industry.

Company Overview

Fortrea is a global contract research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies throughout the clinical development lifecycle. The organization specializes in clinical trial management, pharmacovigilance, regulatory support, and data science services that help bring new medicines and therapies to patients faster.

With decades of experience in clinical development, Fortrea partners with healthcare companies worldwide to manage clinical trials, monitor drug safety, and ensure compliance with international regulatory standards. The company operates across multiple therapeutic areas including oncology, cardiovascular diseases, neurology, immunology, and rare diseases.

Fortrea’s pharmacovigilance and safety science teams play a critical role in monitoring adverse events, analyzing safety signals, and ensuring medicines meet global regulatory safety requirements. Through its global network of safety experts and clinical researchers, the organization contributes to improving patient outcomes and ensuring the safe use of medicines across international markets.

Employees working at Fortrea gain exposure to advanced safety reporting systems, global clinical trial environments, and regulatory frameworks used by leading pharmaceutical companies worldwide.

Job Role & Responsibilities

The Safety Science Analyst supports pharmacovigilance and clinical safety operations by assisting with the collection, processing, and reporting of safety data related to pharmaceutical products.

Key responsibilities include:

• Performing intake and triage of incoming safety reports from clinical trials and spontaneous reporting systems
• Processing adverse event reports according to regulatory guidelines and company procedures
• Entering safety data into adverse event tracking systems and pharmacovigilance databases
• Preparing patient narratives that summarize safety case information
• Coding adverse events using the MedDRA dictionary where applicable
• Supporting assessment of listedness against product labeling for marketed products
• Generating queries to obtain missing or inconsistent safety information
• Coordinating with medical reviewers and pharmacovigilance staff to resolve case queries
• Submitting expedited serious adverse event (SAE) reports to clients, investigators, and regulatory authorities
• Supporting submission of periodic safety reports and regulatory documentation
• Assisting with reconciliation of clinical safety databases
• Maintaining documentation related to global adverse event reporting requirements
• Supporting archival and documentation management for safety case files
• Ensuring compliance with internal quality systems, including SOPs and work instructions
• Collaborating with cross‑functional teams within pharmacovigilance and clinical safety departments

This role ensures that adverse event data is captured accurately and reported within regulatory timelines, helping protect patient safety and maintain compliance with global drug safety regulations.

Eligibility / Qualifications

Candidates applying for this pharmacovigilance and clinical safety role should meet the following requirements.

Required Education

Candidates must hold a healthcare or life sciences degree.

Relevant courses include:

B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, Nursing, Pharmacology, Clinical Research, Life Sciences

Experience

• 0–1 year of experience in pharmacovigilance or drug safety operations
• Freshers with healthcare or pharmacy backgrounds are eligible to apply

Required Skills

• Strong attention to detail when handling clinical safety data
• Good written and verbal communication skills
• Ability to manage multiple safety cases and deadlines
• Knowledge of pharmacovigilance processes and adverse event reporting
• Familiarity with Microsoft Office tools and data entry systems
• Ability to work collaboratively in clinical safety teams

Preferred Knowledge

• Basic understanding of MedDRA coding and pharmacovigilance terminology
• Awareness of regulatory safety reporting guidelines

Location & Salary

Job Location: Pune, Maharashtra, India
Work Model: Office based role

This position is offered as a 6‑month contract opportunity within Fortrea’s clinical safety operations team.

Salary details for this position have not been publicly disclosed. Compensation typically depends on company policy and the candidate’s educational background or prior safety experience.

Application Process

Candidates interested in this pharmacovigilance job opportunity can apply through the official Fortrea careers portal.

Apply here:

https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Pune/Safety-Science-Analyst–6-Month-Contract—Pune—HCP-only-_26902

Applicants are advised to submit their applications through the official website to ensure authenticity and avoid recruitment scams.

Frequently Asked Questions

What does a Safety Science Analyst do?

A Safety Science Analyst processes adverse event reports, enters safety data into pharmacovigilance systems, prepares patient narratives, and supports regulatory reporting for clinical trials and marketed medicines.

Who can apply for this role?

Candidates with healthcare or pharmacy degrees such as B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, or Nursing can apply.

Is this role suitable for freshers?

Yes. Candidates with 0–1 year of safety or pharmacovigilance experience can apply for this role.

What systems are commonly used in pharmacovigilance roles?

Pharmacovigilance professionals typically work with safety databases, adverse event reporting systems, and coding dictionaries such as MedDRA.

How can I apply for this job?

Candidates can apply through the official Fortrea careers website using the application link provided above.

Job Summary

Company	Fortrea
Vacancies	Safety Science Analyst
Required Education	B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, Nursing, Pharmacology, Clinical Research, Life Sciences
Experience	0–1 year pharmacovigilance or safety experience

Tagged as: pharma jobs in pune