Instagram
youtube
Facebook

17609-Associate Safety Project Mgr

3-5 years
Not Disclosed
10 July 3, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Associate Safety Project Manager – Zagreb, Croatia

Employer: IQVIA | Location: Zagreb | Work Mode: On-site

Job Summary:

IQVIA is seeking an experienced Associate Safety Project Manager to lead and deliver high-impact pharmacovigilance and lifecycle safety projects across global clinical and post-marketing studies. In this pivotal role, you will be the client-facing safety SME, managing end-to-end project operations including planning, budgeting, compliance, stakeholder communication, and cross-functional collaboration. Join a healthcare intelligence leader where your expertise shapes global drug safety and patient outcomes.


Key Responsibilities:

  • Lead customer communication and serve as the primary point of contact for assigned safety projects

  • Oversee project planning, scope, timeline, and quality management

  • Manage project financials: revenue recognition, invoicing, and budget monitoring

  • Represent Lifecycle Safety in cross-functional governance and client strategy discussions

  • Serve as the SME for pharmacovigilance and lifecycle safety operations

  • Support the development of safety-related proposals and defend strategies in client meetings

  • Collaborate with internal teams and senior leadership to ensure operational excellence

  • Deliver presentations and contribute to the creation of client-facing material

  • Monitor and report key project performance metrics at both individual and portfolio level


Required Skills & Qualifications:

  • Bachelor’s degree in Life Sciences, Healthcare, or related discipline

  • 3–5 years of experience in clinical research within a CRO

  • Minimum 3 years in Lifecycle Safety (e.g., PV, CEVA, Risk Management)

  • At least 2 years of project management experience in safety operations

  • Strong command of GCP, ICH guidelines, and global PV regulations

  • Exceptional communication, presentation, and stakeholder management skills

  • Proficiency in financial planning, analytics, and tactical project delivery

  • Effective leadership and relationship-building skills in a matrix environment

  • Note: Visa sponsorship is not available for this role


Perks & Benefits:

  • Competitive compensation package (specific salary not disclosed)

  • Opportunity to manage high-profile global safety projects

  • Cross-functional leadership exposure in a top-tier CRO

  • Career advancement and international project portfolio

  • Work alongside global experts in pharmacovigilance and clinical operations


Company Description:

IQVIA is a global leader in healthcare intelligence and clinical research services. With expertise spanning clinical development, real-world evidence, and drug safety, IQVIA empowers life sciences companies to accelerate innovation and improve global health outcomes. Backed by data, analytics, and technology, IQVIA delivers smarter, faster insights to solve the industry’s biggest challenges.


Work Mode:

On-site – Zagreb, Croatia


Call to Action:

Are you ready to drive impactful safety outcomes in a global clinical research powerhouse? Apply today for the Associate Safety Project Manager role at IQVIA and lead with purpose in the future of pharmacovigilance.