Syneos Health hiring Associate Director Safety PV 2026. Check eligibility, responsibilities, skills and apply for Gurugram pharma leadership job opportunity today.
Introduction
Senior professionals looking to advance their leadership career in pharmacovigilance and drug safety can explore this excellent opportunity. The Associate Director – Safety & Pharmacovigilance at Syneos Health is a high-impact role focused on team leadership, project oversight, and global safety operations. This position offers the chance to work on complex clinical safety programs while contributing to better patient outcomes worldwide.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Associate Director – Safety & Pharmacovigilance |
| Company Name | Syneos Health |
| Location | Gurugram, India |
| Employment Type | Full-Time (Office-Based) |
| Department | Safety & Pharmacovigilance |
| Experience Required | Experienced Professionals |
| Education | Life Sciences / Nursing / Related Field |
| Salary | As per company standards |
Company Overview
Syneos Health is a globally recognized organization offering integrated clinical and commercial services to pharmaceutical and biotechnology companies. With a strong focus on innovation and collaboration, the company helps accelerate drug development and improve healthcare outcomes. Syneos Health is known for its supportive culture, global exposure, and commitment to employee growth.
Job Location & Employment Type
- Location: Gurugram, India
- Work Mode: Office-Based
- Employment Type: Full-Time
Open Positions / Department Details
- Department: Safety & Pharmacovigilance
- Role Level: Associate Director
- Focus Area: Clinical safety operations, pharmacovigilance, team leadership
Key Roles & Responsibilities
As an Associate Director – Safety & Pharmacovigilance at Syneos Health, you will:
- Act as a key interface between sponsors, internal teams, and external stakeholders
- Lead and manage Safety & PV teams, including hiring, training, and performance management
- Provide operational oversight for multiple safety projects and ensure timely delivery
- Monitor team performance and maintain quality standards as per Safety Management Plans
- Oversee budgeting, invoicing, and financial aspects of safety projects
- Ensure accurate reporting and communication with clients, acting as an escalation point when needed
- Collaborate with cross-functional teams to ensure timely submission of safety reports
- Participate in SOP development, review, and implementation
- Drive process improvements to enhance efficiency and compliance
- Support business development activities and proposal preparation
- Review clinical safety sections in study protocols and CRFs
- Ensure compliance with global regulations including GCP, ICH guidelines, and GVP modules
- Participate in audits, inspections, and quality improvement initiatives
Eligibility Criteria
Education
- Bachelor’s degree in biological sciences, healthcare, or nursing
- Equivalent qualifications with relevant experience may be considered
Experience
- Significant experience in pharmacovigilance or drug safety
- Proven leadership and team management experience
- Experience in CRO (Clinical Research Organization) environment preferred
Skills Required
- Strong knowledge of pharmacovigilance and safety reporting regulations
- Understanding of GCP, ICH guidelines, and global safety standards
- Leadership and project management expertise
- Financial management and budgeting knowledge
- Excellent communication and stakeholder management skills
- Ability to manage multiple projects in a dynamic environment
- Proficiency in MS Office and project management tools
Salary & Benefits
- Salary: As per company standards
- Leadership role with global exposure
- Opportunity to manage large-scale safety projects
- Career growth into senior management positions
- Professional development and training programs
- Collaborative and inclusive work culture
Selection Process
The selection process typically includes:
- Application screening
- Technical and leadership interviews
- Managerial or client-facing round
- HR discussion
Candidates with strong leadership and pharmacovigilance expertise will be preferred.
How to Apply
Interested candidates can apply through the official Syneos Health careers portal.
- Apply as soon as possible (no fixed deadline mentioned)
Important Dates
- Last Date: Not specified (early application recommended)
Why Apply for This Job?
The Associate Director – Safety & Pharmacovigilance at Syneos Health is an excellent opportunity for experienced professionals to step into a strategic leadership role. Key benefits include:
- Lead global pharmacovigilance operations
- Work with international clients and regulatory frameworks
- Enhance leadership and strategic decision-making skills
- Gain exposure to high-level safety and compliance projects
- Build a long-term career in drug safety and clinical research
FAQs
1. Who can apply for this role?
Experienced professionals with a background in pharmacovigilance or drug safety can apply.
2. Is leadership experience required?
Yes, leadership and team management experience are important for this role.
3. What is the salary offered?
Salary is based on company standards and experience level.
4. Is CRO experience necessary?
CRO experience is preferred but not mandatory.
5. What are the key skills required?
Pharmacovigilance knowledge, leadership, project management, and regulatory compliance are essential.
Conclusion
The Associate Director – Safety & Pharmacovigilance at Syneos Health is a premium opportunity for professionals aiming to lead safety operations in the pharmaceutical industry. With strong career growth, global exposure, and leadership responsibilities, this role can significantly elevate your career. Apply now to take the next step.
Disclaimer
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