Pharmacovigilance Jobs – Parexel, a leading global clinical research organization (CRO), is hiring a Pharmacovigilance Services New Associate in Bengaluru, Karnataka.
This entry-level, full-time role is ideal for B.Pharm graduates with 0–1 year experience seeking to start a career in pharmacovigilance, drug safety surveillance, case processing, ICSR management, MedDRA coding, and regulatory compliance in clinical research services.
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About the Company
Parexel is a premier global biopharmaceutical services provider offering end-to-end solutions across clinical development, regulatory affairs, pharmacovigilance, consulting, and market access. With a deep focus on patient-centric innovation, Parexel partners with biopharma companies to accelerate drug development and commercialization.
The organization emphasizes scientific expertise, regulatory excellence, operational agility, and a strong culture of inclusion, learning, and impact. Parexel’s Pharmacovigilance Services team supports global clients in detecting, assessing, and preventing adverse effects to ensure medicine safety and compliance.
Job Details
- Company Name: Parexel
- Position: Pharmacovigilance Services New Associate
- Experience: 0–1 Year
- Qualification: Bachelor of Pharmacy (B.Pharm)
- Location: Bengaluru, Karnataka, India
- Work Type: Full-time (may involve rotational shifts)
- Job Category: Pharmacovigilance & Drug Safety Surveillance
Job Description
This entry-level role supports Parexel’s Life Sciences R&D vertical in pharmacovigilance and drug safety surveillance. The associate will handle routine case processing tasks under supervision, ensuring accuracy, compliance, and timely delivery in a fast-paced, global clinical research environment.
Pharmacovigilance Services New Associate
- Department: Life Sciences R&D – Pharmacovigilance Services
- Market: Clinical Research & Drug Safety – Biopharmaceuticals
- Role: Pharmacovigilance Services New Associate
- Experience: 0–1 Year
- Education/Qualification: Bachelor of Pharmacy (B.Pharm)
Skills/Qualifications
- Basic understanding of pharmacovigilance processes and drug safety principles
- Ability to follow detailed instructions and SOPs
- Strong attention to detail and accuracy in data handling
- Good communication skills (verbal & written)
- Proficiency in MS Office and willingness to learn safety databases
- Ability to work in rotational shifts and handle routine tasks
- Eagerness to learn and grow in a regulated environment
Key Responsibilities
- Perform case identification, data entry, MedDRA coding, and case processing for ICSRs
- Manage case follow-ups, narrative writing, and regulatory submissions
- Ensure compliance with client guidelines and global regulations (ICH, GVP)
- Support quality checks, query resolution, and documentation
- Assist in literature monitoring, digital platform monitoring, and reconciliations
- Collaborate with team members to meet timelines and quality standards
- Complete assigned tasks and report challenges to supervisors
Benefits/Perks
- Structured training and skill development in pharmacovigilance
- Career progression in Parexel’s Life Sciences R&D vertical
- Exposure to global clinical trials and drug safety operations
- Inclusive, supportive culture with focus on well-being
- Competitive compensation and rotational shift allowances
- Opportunity to contribute to patient safety and innovative therapies
How to Apply
Apply directly through the Parexel careers portal: https://jobs.parexel.com (search for Job ID R0000038973 or “Pharmacovigilance Services New Associate Bengaluru”).
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Parexel Career page.
Submit your updated resume highlighting B.Pharm qualification and any relevant internships, projects, or coursework. For more pharmacovigilance jobs, drug safety associate roles, B.Pharm fresher openings, and clinical research careers in Bengaluru, visit Pharma Recruiter.
Apply now and begin your journey in pharmacovigilance with Parexel – a trusted partner in global drug development!
Why You Should Join
Parexel offers an ideal entry point for B.Pharm graduates to build expertise in pharmacovigilance and drug safety in a global CRO environment.
With comprehensive training, exposure to real-world clinical trial safety data, rotational shift experience, and clear career pathways, the role provides strong professional growth, skill development, and the opportunity to contribute to patient safety worldwide.
Joining Parexel means working in a collaborative, values-driven organization that values innovation, inclusion, and meaningful impact on healthcare.
FAQs
Are freshers eligible for the Pharmacovigilance Services New Associate role?
Yes—0–1 year experience is acceptable; B.Pharm graduates are ideal, even without prior PV experience.
Will this role involve shift work?
Yes—the position may require rotational shifts to support global client timelines and pharmacovigilance operations.
What key skills are required?
Attention to detail, basic pharmacovigilance knowledge (case processing, MedDRA coding), and willingness to learn safety databases and regulatory guidelines.
How do I apply?
Search Job ID R0000038973 on Parexel careers portal and submit your resume directly; shortlisted candidates will be contacted.
