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Associate Safety Project Mgr

3-5 years
Not Disclosed
10 June 9, 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

 

Job Title:

Associate Safety Project Manager

Location:

Zagreb, Croatia

Job Type:

Full-time

Work Mode:

On-site


Job Summary

IQVIA is hiring an experienced Associate Safety Project Manager in Zagreb to lead and manage global Lifecycle Safety (Pharmacovigilance) projects across clinical trial and post-marketing phases. This is an exciting opportunity for professionals with strong project management and pharmacovigilance experience to oversee critical safety deliverables, collaborate with global teams, and ensure quality excellence in service delivery to top pharmaceutical clients.


Key Responsibilities

  • Serve as the main customer interface for assigned safety projects and programs.

  • Oversee customer deliverables including scope, quality, timeline, and financial management.

  • Lead financial tracking including budget updates, invoicing, and revenue recognition.

  • Act as a Safety Subject Matter Expert (SME) to drive strategy, solution design, and pricing discussions.

  • Coordinate internal and external stakeholder meetings and provide regular project updates.

  • Partner with Lifecycle Safety Operations to ensure project alignment with customer needs.

  • Analyze and address evolving customer requirements with innovative PV solutions.

  • Report portfolio-level metrics and ensure oversight on all assigned accounts.


Required Skills & Qualifications

  • Bachelor's degree in Life Sciences, Healthcare, or Project Management.

  • 3–5 years of clinical research experience (CRO setting preferred).

  • Minimum 3 years in Lifecycle Safety (Pharmacovigilance, CEVA, Medical Information, Risk Management).

  • At least 2 years of project management experience.

  • Proficiency in GCP, ICH guidelines, and regulatory compliance.

  • Strong leadership, communication, and stakeholder management skills.

  • Ability to manage multiple projects in a matrix environment.

  • Effective budgeting, forecasting, and financial analysis abilities.

  • Excellent English (written and verbal) skills.


Perks & Benefits

  • Opportunity to work on global, large-scale PV projects.

  • Career advancement pathways in clinical research and drug safety.

  • Collaborative and knowledge-driven global teams.

  • Exposure to cutting-edge PV systems and tools.

  • Employee-centric work culture focused on growth and innovation.


About IQVIA

IQVIA is a global leader in providing clinical research services, real-world healthcare insights, and technology solutions to the life sciences industry. With a presence in over 100 countries, IQVIA connects data and expertise to drive better healthcare outcomes worldwide.


Work Mode

On-site – Zagreb, Croatia


Call to Action

Ready to elevate your pharmacovigilance project management career? Apply now to join IQVIA and contribute to global drug safety and clinical excellence!


Note:

No specific salary or compensation range was mentioned in the job description.