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Associate Medical Director, Cardiology

4-5 years
$112,000 – $312,000
10 Oct. 29, 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:

  • Primary: Durham, North Carolina (Home-Based)

  • Additional: North Carolina


Employment Type:

Full-Time


Job ID:

R1506571


Company Overview:

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We connect data, technology, and expertise to accelerate the development and commercialization of innovative medical treatments — improving patient outcomes and global health.
🔗 Learn more: https://jobs.iqvia.com


Job Overview:

The Associate Medical Director provides medical, clinical, and scientific expertise across all IQVIA divisions. This role involves participating in clinical trial design, execution, and delivery, as well as contributing to business development activities and serving as a global medical expert.


Key Responsibilities:

1. Medical Monitoring

  • Serve as Global Medical Advisor for assigned projects.

  • Act as Scientific Advisor, guiding Project Leaders on medical and scientific aspects.

  • Support investigative sites and project staff with protocol-related issues (clarifications, inclusion/exclusion criteria, patient safety, eligibility).

  • Conduct medical reviews of:

    • Protocols

    • Investigator’s Brochure (IB)

    • Case Report Forms (CRFs)

  • Deliver therapeutic area training to clinical teams.

  • Attend and present at Investigator Meetings.

  • Review and clarify trial-related Adverse Events (AEs).

  • Perform medical case review of Serious Adverse Events (SAEs) in collaboration with Pharmacovigilance.

  • Provide medical input for the Analysis of Similar Events (AOSE).

  • Review adverse event coding and Clinical Study Reports (CSRs) including patient narratives.

  • Participate in Kick-Off meetings, team meetings, and client calls.

  • Be available 24/7 for urgent protocol-related questions (as per local labor laws).

  • May require regular travel.


Technical & Physical Requirements:

  • Frequent keyboard use (repetitive finger motion).

  • Extensive communication (telephone and in-person).

  • Must ensure clear and accurate speech perception.


Qualifications:

Education:

  • Medical Degree (MD or equivalent) from an accredited and internationally recognized institution.

  • Board Certification in Cardiology or relevant specialty required/preferred.

Experience:

  • Minimum 5 years of experience in clinical medicine.

  • Minimum 4 years of experience in clinical trials (as investigator or in Pharma/CRO/Biotech).

  • In-depth understanding of scientific, clinical, regulatory, and commercial landscapes in the therapeutic area.

  • Knowledge of federal and local clinical research regulations.

  • Strong business acumen and cross-functional collaboration skills.


Compensation:

💰 Annual Base Pay Range: $112,000 – $312,000
(Actual pay depends on education, experience, skills, and location.)

Additional benefits may include:

  • Incentive plans and bonuses

  • Comprehensive health and welfare benefits

  • Retirement and savings plans


Equal Employment Opportunity (EEO):

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration without regard to:

  • Race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
    🔗 Learn more: https://jobs.iqvia.com/eoe


Application Link:

👉 Apply Now