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Program Manager: Pharmacovigilance, Safety, Medical- Hyderabad (Hybrid)

Syneos Health
Syneos Health
7-12 years
preferred by company
10 Jan. 19, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Job Title: Program Manager – Pharmacovigilance, Safety, Medical (Hybrid – Hyderabad)
Company: Syneos Health
Location: Madhapur, Telangana, India
Employment Type: Full-Time, Hybrid
Experience Required: 7–12 years in Pharmacovigilance, Safety, or Life Sciences Program Management
Job ID: 25103898
Updated: December 18, 2025


Job Overview

Syneos Health®, a leading global biopharmaceutical solutions organization, is seeking a Program Manager to lead strategic initiatives in Pharmacovigilance, Safety, and Medical programs. This role will drive cross-functional, complex programs, ensuring alignment with organizational objectives, regulatory compliance, and timely delivery of high-impact outcomes.

As part of the Technology & Data Solutions (TDS) business unit, you will manage advanced technology solutions, M&A initiatives, and innovative data platforms to accelerate drug development and enhance patient outcomes.


Key Responsibilities

  • Lead end-to-end program management for a portfolio of Pharmacovigilance, Safety, and Medical initiatives, ensuring adherence to budget, timelines, and scope.

  • Develop program strategies, define goals, track progress, and proactively mitigate risks.

  • Manage interdependencies between multiple projects, optimizing resource allocation and prioritization.

  • Oversee project managers and cross-functional teams, providing guidance, mentorship, and leadership to achieve program objectives.

  • Serve as the primary liaison between business stakeholders, technical teams, and leadership to ensure program alignment with organizational goals.

  • Establish program procedures, guidelines, and reporting structures; approve modifications within area of responsibility.

  • Support benefits management, SOW/PO tracking, and vendor relationships for technology-enabled initiatives.

  • Monitor the impact of changes in project scope or resource allocation and implement effective strategies to ensure successful outcomes.

  • Drive collaboration, stakeholder engagement, and conflict resolution across diverse teams.

  • Ensure compliance with regulatory requirements, organizational standards, and global life sciences best practices.


Required Qualifications & Experience

  • Bachelor’s degree in a technical, pharmaceutical, life sciences, or related discipline. Advanced degrees preferred.

  • 7–12 years of experience in program or portfolio management, with at least 5 years in Pharmacovigilance, Safety, or Medical affairs programs.

  • Proven track record of managing complex programs, delivering results on time and within budget.

  • Strong understanding of clinical development processes, safety reporting, and regulatory compliance in the pharmaceutical industry.

  • Experience managing cross-functional teams, vendors, and global stakeholders.

  • Excellent leadership, strategic thinking, and problem-solving skills.

  • Advanced knowledge of project management tools, methodologies, and enterprise systems.

  • PMP certification or equivalent preferred.


Key Skills

  • Exceptional communication and interpersonal skills, capable of engaging with senior leadership and stakeholders.

  • Strong analytical, organizational, and decision-making capabilities.

  • Ability to navigate ambiguity and manage multiple priorities in a fast-paced environment.

  • High proficiency in risk management, budgeting, and resource planning.

  • Collaborative mindset with experience in driving change management initiatives.


Why Join Syneos Health?

  • Work with a global organization supporting 94% of novel FDA-approved drugs and 95% of EMA-authorized products.

  • Exposure to cutting-edge technology, data, and pharmacovigilance innovations that accelerate patient access to medicines.

  • Career development through mentorship, technical training, and leadership opportunities.

  • Inclusive culture fostering diversity, belonging, and continuous learning.


Apply now on ThePharmaDaily.com to advance your career in Pharmacovigilance and Medical Program Management with a global leader in life sciences.