Paraxel Hiring Fresher for Patient Safety Associate I: PV Jobs 2026
Paraxel, a global clinical research organization, is hiring for the role of Patient Safety Associate I at its Mohali and Hyderabad locations. This opportunity is ideal for B.Pharm and M.Pharm graduates with 0–2 years of experience who are looking to start or build their career in pharmacovigilance and drug safety operations.
The role focuses on supporting safety case processing, adverse event management, safety data review, and compliance with global pharmacovigilance regulations. Candidates will work within a structured, regulated environment, collaborating with global teams to ensure high‑quality patient safety outcomes.
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🏢 About the Organization
Paraxel is a globally recognized organization providing clinical research, regulatory consulting, and pharmacovigilance services to pharmaceutical and biotechnology companies worldwide. The company works within highly regulated environments and supports patient safety activities across the entire drug development lifecycle. Working at Parexel provides exposure to global safety systems, regulatory frameworks, and structured PV operations.
📊 Position Overview
- Position: Patient Safety Associate I
- Department:PV
- Location: Hyderabad, Mohali India
- Experience: 0 to 2 Years
- Qualification: B.Pharm, M.Pharm
- Job Type: Full-Time
📋 Main Responsibilities – Patient Safety Associate I
- Monitor incoming safety reports from multiple sources including mailboxes, EudraVigilance (EV), and biomedical literature searches.
- Perform literature searches as per defined search strategies and identify valid cases for entry into the safety database.
- Triage incoming reports to assess completeness, legibility, and case validity, including review of abstracts, articles, and citations.
- Create safety cases in the pharmacovigilance database, perform accurate data entry, and advance cases through defined workflow steps.
- Compare and analyze affiliate‑reported data against information available in the client system to ensure consistency.
- Review cases for medical cohesiveness and consistency.
- Perform product coding, ensure accurate MedDRA coding in accordance with MedDRA Term Selection: Points to Consider.
- Assess seriousness, causality, and expectedness of reported events.
- Prepare medically sound case narratives based on reported safety information.
- Initiate and manage case follow‑up queries as required.
- Perform quality and validation checks to ensure case accuracy and regulatory compliance.
- Support ICSR compliance activities, including late case investigations, root‑cause analysis for delays, and collection of supporting documentation.
- Prepare required ADR forms or coversheets.
- Support expedited reporting procedures, quality review of line listings and tabulations, and adherence to local safety reporting requirements.
- Register products and organizations with regulatory authorities for electronic reporting on behalf of sponsors.
- Maintain product records including new product additions, removal of withdrawn products, expired licenses, or MAH transfer updates in client systems.
- Generate, report, and reconcile compliance metrics in collaboration with internal teams, clients, and external partners.
- Support additional PV activities such as End of Study Unblinding (EOSU), case corrections, case deletion/deactivation requests, recoding activities, MAH reporting, safety notifications, Patient Oriented Programs (POP), and Social Media safety activities, as applicable.
- Complete assigned tasks within timelines and report challenges or risks promptly to supervisors.
🎓 Required Qualification
- Education: B.Pharm, M.Pharm, or Pharm.D only.
- Experience: 0–2 years of experience in pharmacovigilance, drug safety, or safety data management.
- Pharmacovigilance Knowledge: Completion of a pharmacovigilance course or certification, or good knowledge of medical terminology and global drug safety regulations.
- Scientific Exposure: Publications in peer‑reviewed scientific journals.
- Digital & AI Skills
- Experience using AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and improve productivity.
- Curiosity to explore responsible and ethical use of AI, including risk management and compliance considerations.
🧠 Essential Skills
- Strong attention to detail to ensure accuracy in safety data processing.
- Solid analytical skills for case assessment and problem resolution.
- Good written and verbal communication skills.
- Ability to collaborate effectively within cross‑functional teams.
- Willingness to learn continuously and adapt to evolving PV processes.
⭐ Role Summary
The Patient Safety Associate I role is a critical entry point into the pharmacovigilance and drug safety domain. Freshers gain exposure to real‑world safety case processing, global regulations, and compliance‑driven workflows. Working at Parexel helps candidates develop a strong foundation in patient safety, regulatory compliance, and clinical research operations, preparing them for long‑term PV careers.
🎯 Suitable Candidates
This opportunity is suitable for:
- B.Pharm / M.Pharm / Pharm.D freshers
- Candidates with 0–2 years of PV or drug safety experience
- Graduates who have completed PV training or certification
- Individuals interested in patient safety and global drug safety roles
📈 Career Opportunities
With experience and continuous learning, professionals can progress into roles such as:
- Patient Safety Associate II
- Pharmacovigilance Associate
- Drug Safety Executive
- Senior Safety Specialist
Parexel also offers long‑term career paths in global safety operations and leadership roles.
💰 Compensation Details
- Expected Salary: Freshers can expect a salary range of ₹3.5–5 LPA
💡 Practical Tips
- Highlight analytical skills and scientific achievements (publications, if any)
- Revise pharmacovigilance fundamentals and ICSR concepts
- Strengthen knowledge of medical terminology and safety regulations
- Be prepared to discuss PV training or academic exposure
🔗 Application Process
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.
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📚 Career Guide
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❓ FAQs-Patient Safety Associate I
1. Who can apply for the Patient Safety Associate I role at Paraxel?
Candidates with B.Pharm or M.Pharm degrees and 0–2 years of experience in pharmacovigilance, drug safety, or related life sciences roles.
2. Is this role suitable for freshers?
Yes. This role is well‑suited for fresh graduates and early‑career professionals looking to start a career in pharmacovigilance and patient safety operations.
3. What are the main responsibilities in this role?
You will support ICSR processing, literature monitoring, MedDRA coding, narrative writing, follow‑up management, compliance activities, and safety database documentation.
4. Will I work on both clinical and post‑marketing safety cases?
Yes. The role involves handling safety cases related to clinical trials as well as post‑marketing products.
5. Which systems or tools will I use?
You will work on pharmacovigilance safety databases, EudraVigilance systems, literature monitoring tools, and internal case processing platforms.
