Senior Clinical Development Medical Director

Novartis

4+ years

$236,400 – $439,600

United States

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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Senior Clinical Development Medical Director

Job Description

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