Senior PV Agreements Specialist – Warsaw (On-site)
IQVIA | Warsaw, Poland
Compensation: Not disclosed | Experience Required: Minimum 3 years
Job Summary
IQVIA is seeking a skilled Senior PV Agreements Specialist to lead pharmacovigilance agreement development and serve as the key customer liaison for safety documentation. Based in Warsaw, this role is ideal for experienced professionals in Lifecycle Safety who are looking to leverage their knowledge in a dynamic and global environment. You'll manage the end-to-end process of PV agreements while mentoring junior team members and ensuring compliance with international safety standards.
Key Responsibilities
Develop and prepare PV (pharmacovigilance) agreements for assigned clients.
Collaborate with project teams to align terms and conditions of safety agreements.
Act as primary customer contact for large-scale or complex safety agreement projects.
Oversee negotiation, finalization, and distribution of PV agreements.
Represent the safety agreements team during client meetings and provide expert input.
Contribute to project planning and budgeting for safety agreement services.
Guide, train, and mentor junior team members involved in PV documentation.
Ensure adherence to internal processes and templates for agreement development.
Required Skills & Qualifications
Bachelor’s degree (preferably in health sciences or related discipline).
Minimum 3 years of experience in Lifecycle Safety (e.g., PV, CEVA, Medical Info, Risk Management).
Proven experience in project management within the pharmacovigilance domain.
Deep understanding of PV processes and safety compliance.
Strong attention to detail and commitment to high-quality standards.
Excellent communication and negotiation skills.
Ability to multitask and work on various projects concurrently.
Strong interpersonal skills to build collaborative relationships across teams and clients.
Perks & Benefits
Work with one of the world’s leading CROs and healthcare intelligence providers.
Exposure to global PV projects and top-tier pharma clients.
Opportunities for career growth and internal mobility.
Collaborative and inclusive work culture.
Access to comprehensive training and development resources.
Company Overview
IQVIA is a global leader in clinical research, real-world evidence, and healthcare data analytics. The company partners with life sciences organizations to bring new treatments to market faster and more efficiently. With a strong focus on innovation and patient safety, IQVIA plays a vital role in advancing global health outcomes.
Work Mode: On-site (Warsaw, Poland)
Preferred Experience: 3+ years in pharmacovigilance or Lifecycle Safety
Ready to take your PV career to the next level?
Apply now and become a part of IQVIA’s mission to power human data science and improve healthcare globally.
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