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Associate Medical Director, Cardiology

4-5 years
$112,000.00 - $312,000.00
10 Oct. 4, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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 Medical Director, Cardiology

📍 Location: Durham, North Carolina
🕒 Employment Type: Full Time
🔢 Job ID: R1506571
🏢 Work Type: Home-based
📍 Additional Locations: North Carolina


🧭 Position Overview

The Associate Medical Director (AMD) provides medical, clinical, and scientific advisory expertise across IQVIA divisions. The role participates in all aspects of Medical Science involvement on assigned trials, serving as a medical expert throughout the project delivery lifecycle. The AMD also supports business development by providing therapeutic and medical expertise.


⚙️ Key Responsibilities

Medical Monitoring & Advisory

  • Serve as Global Medical Advisor on assigned projects.

  • Act as Scientific Advisor to Project Leaders on medical and scientific matters.

  • Provide medical support to investigative sites and project staff regarding protocols, inclusion/exclusion criteria, and patient safety.

  • Review protocols, Investigative Drug Brochures (IDB), and Case Report Forms (CRFs).

  • Deliver therapeutic area/indication training to clinical project teams.

  • Attend and present at Investigator Meetings.

  • Review and clarify trial-related Adverse Events (AEs) and Serious Adverse Events (SAEs) in collaboration with Pharmacovigilance teams.

  • Provide medical support for Analysis of Similar Events (AOSE) and adverse event coding.

  • Review Clinical Study Reports (CSR) and patient narratives.

  • Participate in Kick-Off meetings, weekly team meetings, and client meetings as required.

  • Be available 24/7 for urgent protocol-related inquiries from investigative sites (per local labor laws).

Communication & Collaboration

  • Extensive use of keyboard, telephone, and face-to-face communication for documentation and project coordination.

  • Work collaboratively with cross-functional teams to ensure clinical and scientific standards are met.

Travel

  • May require regular travel as part of project responsibilities.


🎓 Qualifications

  • Education: Medical degree from an accredited and internationally recognized medical school relevant to general medical education.

  • Experience:

    • Minimum 5 years in clinical medicine.

    • At least 4 years of clinical trials experience as an investigator or within Pharma, CRO, or Biotech.

  • Certification: Specialty Board certification required; preferred in the therapeutic area (Cardiology).

  • Knowledge:

    • Scientific, clinical, regulatory, and commercial landscape in the relevant therapeutic area.

    • Applicable federal and local clinical research regulations and guidelines.

  • Business Acumen: Understanding of clinical trial operations, regulatory compliance, and healthcare industry standards.


🌍 About IQVIA

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, connecting data, technology, and expertise to accelerate the development and commercialization of innovative medical treatments.

🔗 Learn more: https://jobs.iqvia.com


⚖️ Equal Employment Opportunity

IQVIA provides equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.


💰 Compensation

  • Base Pay Range (Annualized): $112,000 – $312,000

  • Additional incentives, bonuses, and benefits may apply.