Safety Physician
Location: Madhapur, Telangana, India
Job ID: 25103796
Updated On: January 20, 2026
Employment Type: Full-time
Work Mode: On-site
About the Company
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success across the clinical development, medical affairs, and commercial landscape. With operations in over 110 countries and a workforce of 29,000+ professionals, Syneos Health partners with global sponsors to deliver innovative therapies that change lives.
Over the past five years, Syneos Health has supported 94% of all novel FDA-approved drugs and 95% of EMA-authorized products, working across 200+ studies, 73,000 sites, and more than 675,000 clinical trial patients worldwide.
Job Overview
Syneos Health is seeking a qualified Safety Physician to join its Pharmacovigilance and Safety team in Hyderabad. The role involves comprehensive medical review of adverse events for investigational and marketed products, ensuring accurate medical interpretation, regulatory compliance, and proactive safety surveillance throughout the product lifecycle.
This position offers an excellent opportunity for medical professionals looking to build or advance a career in pharmacovigilance within a global biopharmaceutical environment.
Key Responsibilities
Perform medical review and clinical assessment of adverse events for clinical trial and post-marketing products
Ensure accurate medical interpretation and consistency in adverse event case evaluation
Maintain working knowledge of MedDRA, WHO-DRL, and safety databases such as ARGUS
Collaborate closely with Safety and Pharmacovigilance teams to support case processing and safety decision-making
Ensure compliance with global regulatory requirements, SOPs, and internal policies
Identify, assess, communicate, and manage potential safety signals and risks
Provide medical input for aggregate safety reports including PSURs, PADERs, and annual safety reports
Liaise with client medical and safety personnel as required
Stay updated on relevant clinical, therapeutic, and drug development information
Support mentoring and training of junior safety and case processing staff
Participate in continuous medical education to maintain pharmacovigilance expertise
Perform additional responsibilities as assigned in line with organizational requirements
Education & Qualifications
M.D., MBBS, or D.O. degree (mandatory)
Completion of an accredited medical residency program
Experience Required
1–2 years of post-residency clinical practice experience (preferred)
Minimum 1 year of experience in the pharmaceutical, biotechnology, or medical device industry within pharmacovigilance, drug safety, or epidemiology (preferred)
Demonstrated knowledge of global pharmacovigilance regulations and reporting processes
Skills & Competencies
Strong understanding of global drug safety regulations and compliance standards
Proficiency in safety databases and Microsoft Office tools (Word, Excel, PowerPoint), Outlook, Visio, and shared content platforms
Excellent verbal and written communication skills in English
Strong analytical, interpersonal, and stakeholder management skills
Ability to effectively communicate medical concepts to cross-functional teams
Willingness to travel up to 10% as required
Why Join Syneos Health
Structured career development and progression opportunities
Supportive leadership and continuous technical and therapeutic training
Inclusive “Total Self” culture promoting diversity, equity, and belonging
Competitive total rewards and recognition programs
Opportunity to work on global, high-impact drug development programs
Additional Information
The responsibilities outlined above are not exhaustive and may evolve based on business needs. Syneos Health reserves the right to modify job responsibilities and qualification requirements as necessary. Equivalent education or experience may be considered. Employment is subject to applicable local laws and regulations, and Syneos Health is committed to equal opportunity employment and reasonable accommodations in compliance with applicable legislation.
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