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Associate Medical Safety Director

2-3 years
Not Disclosed
10 July 18, 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 Medical Safety Director – Belgrade

Job Summary:
IQVIA is hiring an experienced Associate Medical Safety Director to join its Lifecycle Safety Medical team in Belgrade. This leadership role is pivotal in ensuring drug safety through signal detection, risk management, and clinical data review for global pharmacovigilance operations. Candidates with a strong background in medicine, clinical practice, and pharmaceutical safety are encouraged to apply for this hybrid opportunity.


Key Responsibilities:

  • Conduct aggregate reviews of safety data and oversee product safety profiles

  • Lead signal detection strategies, analysis, and safety evaluation reports

  • Review and contribute to IND Annual Reports, PBRERs, PSURs, DSURs, and other periodic safety documents

  • Provide input into Risk Management Plans and label safety updates

  • Support benefit-risk assessments in both clinical trial and post-marketing settings

  • Perform medical review of AEs and ADRs, including narrative and causality assessment

  • Represent medical safety in internal and external stakeholder meetings

  • Support Safety Governance and other PV-related discussions


Required Skills & Qualifications:

  • Medical degree from an accredited institution

  • Minimum 3 years clinical practice + 2 years in pharmaceutical industry or equivalent

  • Strong knowledge of GVP, ICH-GCP, and global safety regulations

  • Hands-on experience in signal detection, aggregate reporting, and benefit-risk evaluation

  • Proficient in medical review, data analysis, and scientific writing

  • Ability to handle multiple projects and meet strict deadlines

  • Effective communication and stakeholder engagement skills

  • Proven ability to collaborate with global teams and provide mentorship


Perks & Benefits:

  • Competitive compensation and performance incentives

  • Hybrid work environment

  • Global exposure with one of the top CROs worldwide

  • Access to cutting-edge tools and global safety projects

  • Career growth in pharmacovigilance and medical safety leadership


Company Description:

IQVIA is a global leader in clinical research and healthcare analytics, delivering intelligent solutions that connect healthcare providers, pharmaceutical companies, and patients. With a presence in over 100 countries, IQVIA is committed to improving healthcare outcomes through innovation and technology-driven insights.


Work Mode: Hybrid (Belgrade)


Call-to-Action:
Ready to advance your career in medical safety and pharmacovigilance? Apply now to join IQVIA’s dynamic global team and make a meaningful impact in patient safety.