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Senior Clinical Development Medical Director

4+ years
$236,400 – $439,600
10 Nov. 26, 2025
Job Description
Job Type: Full Time Hybrid 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: Senior Clinical Development Medical Director – Cardiovascular Programs
Company: Novartis Pharmaceuticals Corporation
Location: East Hanover, New Jersey, USA (Hybrid)
Job Type: Full-Time | Senior Level | Clinical Development
Job ID: REQ-10062628

About Novartis:
Novartis is a global biopharmaceutical leader committed to transforming patient care through innovative medicines and therapies. Our work spans clinical research, development, and commercialization, with a focus on delivering meaningful outcomes in complex therapeutic areas. We foster a culture of collaboration, scientific excellence, and operational integrity, empowering our teams to innovate and excel.

Role Overview:
The Senior Clinical Development Medical Director (CDMD) will lead the strategic planning, execution, and oversight of clinical programs in the Cardiovascular Therapeutic Area, with a focus on anticoagulation. This role ensures end-to-end clinical development excellence across phases I–IV, integrating scientific insight, regulatory alignment, and operational execution in a global, matrixed environment. The CDMD will drive clinical strategy, support cross-functional decision-making, and mentor teams to achieve program objectives.

Key Responsibilities:

  • Provide clinical leadership and strategic medical input for all deliverables within assigned programs.

  • Lead development and review of clinical sections of regulatory documents including protocols, Clinical Development Plans (CDP), and Integrated Development Plans (IDP).

  • Oversee the execution of clinical trials in collaboration with Global Trial Directors (GTDs), regional medical associates, and cross-functional stakeholders.

  • Support program safety monitoring and act as a core member of the Safety Management Team (SMT) where applicable.

  • Serve as a scientific advisor to internal and external stakeholders, including regulatory authorities and decision boards.

  • Contribute to the development of clinical standards and disease-specific protocols in alignment with global guidelines.

  • Mentor and guide junior clinical staff within the program or department.

Required Experience & Qualifications:

  • MD or equivalent medical degree with advanced clinical training. Board certification or eligibility preferred.

  • Minimum 4 years of clinical practice experience including residency, with extensive experience in clinical research and drug development.

  • Proven track record in planning, executing, and publishing clinical trials across global/matrixed pharmaceutical environments (Phases I–IV).

  • Strong expertise in disease area (Cardiovascular/Anticoagulation), clinical trial design, statistics, and regulatory requirements.

  • Experience interpreting and presenting efficacy and safety data for clinical trials.

  • Demonstrated ability to build effective scientific partnerships with internal and external stakeholders.

  • Previous global people management or matrix team leadership experience preferred.

  • Excellent communication, problem-solving, and strategic planning skills.

Compensation & Benefits:

  • Expected salary range: $236,400 – $439,600 per year (commensurate with experience and skills).

  • Performance-based cash incentives and potential eligibility for annual equity awards.

  • Comprehensive benefits package including health, life, and disability insurance, 401(k) with company match, and generous leave policies.

Why Join Novartis:

  • Lead groundbreaking cardiovascular clinical programs and make a direct impact on patient care.

  • Collaborate with global experts in a fast-paced, purpose-driven environment.

  • Access to career development, mentoring, and continuous learning opportunities.

  • Contribute to a culture that values scientific excellence, collaboration, and innovation.

Equal Opportunity & Accessibility:
Novartis is an Equal Opportunity Employer and provides reasonable accommodations for individuals with disabilities. We do not discriminate based on legally protected characteristics.

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