MBBS Job Opportunity: Apply for a Safety Physician Role at Syneos Health!
Looking for an MBBS job in global pharmacovigilance? Syneos Health is offering an excellent opportunity for qualified physicians to work as a Safety Physician, contributing to drug safety, adverse event review, and regulatory compliance in a leading biopharmaceutical organization.
Job Details:Â
- Job Position: Safety Physician
- Location: Telangana
About the Company:
Syneos Health is a leading, fully integrated biopharmaceutical solutions organization built to accelerate customer success. Known globally for innovation in clinical development, Syneos Health careers span across medical, regulatory, and commercial domains. The company operates in over 110 countries with more than 29,000 employees and has supported 94% of all Novel FDA-approved drugs and 95% of EMA-authorized products in the last five years.
Qualifications:
- M.D., MBBS, or D.O. degree
- Completion of an accredited residency
- Minimum 1–2 years of clinical practice experience preferred
- At least 1 year of experience in pharmaceutical, biotechnology, or pharmacovigilance roles preferred
- Strong knowledge of global pharmacovigilance regulations and safety processes
- Proficiency in Microsoft Office Suite, Outlook, Visio, safety databases, and shared workspaces
- Excellent verbal and written communication skills in English and the relevant local language
- Strong interpersonal, presentation, and influencing abilities
- Ability to travel up to 10%
Job Description:
This MBBS job at Syneos Health is ideal for physicians seeking to transition into pharmacovigilance and drug safety roles. The Safety Physician is responsible for medical review of adverse events related to investigational and marketed products while ensuring compliance with global safety regulations and internal SOPs. This role is well-suited for professionals exploring long-term physician jobs beyond traditional clinical practice.
Key Responsibilities:
- Performs medical review of adverse events reported for investigational and marketed products
- Maintains familiarity with MedDRA, WHO-DRL, and safety databases such as ARGUS
- Works closely with Safety and Pharmacovigilance (SPVG) colleagues to ensure accurate medical interpretation
- Ensures regulatory and SOP compliance for clinical and post-marketing safety surveillance
- Identifies, communicates, and manages potential safety issues effectively
- Interacts with client safety and medical personnel as required
- Stays updated with clinical and drug development information relevant to ongoing programs
- Provides medical review and interpretation for aggregate safety reports such as PSURs, PADERs, and annual safety reports
- Maintains pharmacovigilance expertise through continued medical education
- Assists as a mentor and trainer for internal safety and case processing teams
- Performs duties in compliance with corporate and departmental policies
- Performs other responsibilities as assigned by management
