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Safety & Pharmacovigilance - Trainee (Contractual | M.Pharm/Pharm.D/Bhms/Bds | 2025 Passout Only)

0-2 years
₹3.5 – 5.5 LPA
10 Aug. 25, 2025
Job Description
Job Type: Full Time Education: M.Pharm/Pharm.D/BHMS/BDS Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Safety & Pharmacovigilance - Trainee (Contractual | M.Pharm/Pharm.D/BHMS/BDS | 2025 Passout only)
Updated: August 21, 2025
Location: IND-Gurugram
Job ID: 25101070

💰 Estimated Salary: ₹3.5 – 5.5 LPA (typical range for PV trainee roles in India, depending on organization and contract terms)


Description

Safety & Pharmacovigilance - Trainee (Contractual | M.Pharm/Pharm.D/BHMS/BDS | 2025 Passout only)
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything we do. We continuously look for ways to simplify and streamline processes to make Syneos Health easier to work with, and easier to work for.

With 29,000 employees across 110 countries, we know one thing for certain: Work Here Matters Everywhere.


Why Syneos Health?

  • Career development and progression opportunities.

  • Supportive and engaged line management.

  • Technical and therapeutic area training.

  • Peer recognition and rewards program.

  • Total Self Culture – fostering diversity, inclusivity, and belonging across all teams.


Job Responsibilities

  • Monitor and route incoming project information.

  • Record, track, and manage ICSR (Individual Case Safety Report) documentation.

  • Redact patient identifiers as per GCP, GVP, and data protection guidelines.

  • Enter or assist in case creation within the safety database.

  • Maintain case conventions and ensure accuracy.

  • Manage translation of documents, file creation, and retention (paper & electronic).

  • Assist with query follow-up, submissions, and workflow reconciliation.

  • Support global/local literature screening and safety review.

  • Contribute to narrative writing, coding (events, history, concomitant meds, MedDRA).

  • Assist with expedited reporting and regulatory submissions.

  • Validate and recode xEVMPD product records.

  • Identify and manage duplicate ICSRs.

  • Participate in SPOR/IDMP-related activities.

  • Ensure documentation compliance with SOPs, TMF, and PV Master File requirements.

  • Collaborate effectively with project team members, internal & external.

  • Participate in audits and apply regulatory intelligence.


Qualification Requirements

Education & Eligibility:

  • M.Pharm, Pharm.D, M.Sc + B.Pharm, BHMS, BDS, or Ph.D. (Pharmacy) – 2025 passouts only.

  • 2024 graduates with a strong interest in Pharmacovigilance may also apply.

Core Skills (Required):

  • Strong scientific/healthcare knowledge base.

  • MS Office proficiency.

  • Strong organizational & documentation skills.

  • Excellent written and verbal communication.

  • Team collaboration and multitasking.

  • High attention to detail.

Preferred Skills:

  • Familiarity with safety databases and PV processes.

  • Knowledge of pharmacology, medical terminology, or MedDRA coding.

  • Experience with collaboration tools (Visio, Team Share, etc.).


Additional Details

  • Contract Duration: 1 year (continuation based on performance & business need).

  • Tasks and responsibilities may evolve as per project requirements.

  • Comprehensive pharmacovigilance training will be provided before project allocation.


Summary

As a Safety & Pharmacovigilance Trainee, you will undergo structured training and contribute to ICSR processing, literature review, MedDRA coding, drug dictionary maintenance, data validation (xEVMPD, SPOR/IDMP), duplicate case management, and regulatory submissions. You will ensure adherence to GCP, GVP, and company SOPs while supporting the global safety team. Based on performance, trainees may transition to full project responsibilities.