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Safety Physician

Syneos Health
Syneos Health
Fresher years
upto 17 LPA
Remote, India, India
10 April 30, 2026
Job Description
Job Type: Remote Education: MBBS 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 Physician – Pharmacovigilance Jobs in Hyderabad & Pune | Syneos Health

Company: Syneos Health
Job Role: Safety Physician
Job Type: Full-Time
Work Mode: Office-Based
Locations: Hyderabad / Pune
Job Requisition ID: 25105747
Experience Required: 1–3 Years
Freshers Eligible: YES


About the Company

Syneos Health is a globally recognized biopharmaceutical solutions organization dedicated to accelerating customer success across the drug development and commercialization lifecycle. The company partners with pharmaceutical, biotechnology, and healthcare innovators to deliver high-quality clinical and pharmacovigilance solutions worldwide.

With a strong global workforce and extensive expertise in clinical research, regulatory affairs, and drug safety, Syneos Health continues to contribute significantly to modern healthcare advancement.


Job Overview

Syneos Health is hiring experienced professionals for the position of Safety Physician in Hyderabad and Pune. This opportunity is ideal for MBBS-qualified professionals with prior pharmacovigilance and clinical practice experience who are looking to build a long-term career in drug safety, medical review, and global pharmacovigilance operations.

The role involves medical review of adverse events, aggregate report assessment, regulatory compliance, and collaboration with cross-functional pharmacovigilance teams to ensure patient safety and product risk management.


Key Responsibilities

  • Perform medical review and assessment of adverse events associated with investigational and marketed pharmaceutical products

  • Conduct safety evaluation and medical interpretation of Individual Case Safety Reports (ICSRs)

  • Collaborate with Safety and Pharmacovigilance teams to ensure consistent and accurate case assessment

  • Ensure compliance with global pharmacovigilance regulations, SOPs, and safety reporting standards

  • Work with safety databases such as ARGUS and coding dictionaries including MedDRA and WHO-DRL

  • Identify and manage potential safety concerns and escalate risks appropriately

  • Contribute to aggregate safety reporting activities including PSURs, PADERs, and annual safety reports

  • Interact with client medical and safety teams for case discussions and medical clarification

  • Stay updated with ongoing developments in clinical research, drug safety, and regulatory guidelines

  • Mentor junior pharmacovigilance professionals and support internal training initiatives


Eligibility Criteria

  • MBBS qualification is mandatory

  • Candidates graduating from foreign universities must possess valid MCI/NMC clearance

  • Completion of an accredited medical residency program preferred

  • Minimum 1 year of experience in Pharmacovigilance is mandatory

  • 1–2 years of clinical practice experience preferred

  • Strong understanding of global pharmacovigilance regulations and drug safety processes

  • Familiarity with safety databases and adverse event coding systems

  • Excellent communication, presentation, and medical writing skills in English

  • Proficiency in Microsoft Office tools including Word, Excel, PowerPoint, and Outlook


Required Skills

  • Medical review and causality assessment

  • Signal detection and safety surveillance

  • Aggregate report writing and interpretation

  • Regulatory compliance and risk management

  • Clinical trial safety monitoring

  • Adverse event case processing knowledge

  • Pharmacovigilance workflow understanding

  • Cross-functional stakeholder communication


Why Join Syneos Health?

  • Opportunity to work with one of the world’s leading CRO and life sciences organizations

  • Exposure to global clinical development and pharmacovigilance projects

  • Strong learning and career growth opportunities in drug safety and medical review

  • Collaborative work environment with experienced healthcare professionals

  • Participation in high-impact pharmaceutical and biotechnology programs worldwide


Important Note for Applicants

This role is not suitable for freshers. Candidates must have prior pharmacovigilance experience and a strong medical background to qualify for this position.

Fresh MBBS graduates looking to enter Pharmacovigilance are encouraged to first gain experience in Drug Safety Associate, Medical Reviewer, or Pharmacovigilance Associate roles before applying for Safety Physician positions.


About Syneos Health Global Impact

Over the past five years, Syneos Health has contributed to:

  • 94% of all Novel FDA Approved Drugs

  • 95% of EMA Authorized Products

  • 200+ Clinical Studies

  • 73,000+ Clinical Trial Sites

  • 675,000+ Trial Patients Globally


How to Apply

Interested candidates can apply directly through the official careers portal of Syneos Health.

For more verified Pharmacovigilance, Clinical Research, Drug Safety, Regulatory Affairs, and Healthcare jobs worldwide, visit ThePharmaDaily.com.