Senior Clinical Development Medical Director - Renal / Senior Clinical Development Medical Director - Renal

Novartis Pharma AG - June 20, 2025

Job ID

REQ-10050166

May 20, 2025

Switzerland

Summary

The Senior Clinical Development Medical Director (CDMD) is accountable for leading the strategic planning and management of assigned clinical program(s) from an end-to-end clinical development perspective. In this role, you will oversee the clinical development for designated programs within the Renal Therapeutic Area (TA) and drive the execution of the clinical development plan. You will create an empowered organization capable of navigating matrix environments and adapting swiftly to business requirements.

About the Role

Major Accountabilities:

Your responsibilities will include, but are not limited to:

  • Providing clinical leadership and strategic medical input for all clinical deliverables within the assigned project or segment of a clinical program.
  • Leading the development of clinical sections of trial and program-level regulatory documents.
  • Driving execution of the assigned clinical program and/or clinical trial in partnership with global line functions, designated Global Trial Directors (GTDs), and regional/country medical associates, where applicable.
  • Supporting the (Senior) Global Program Clinical Head (GPCH) in ensuring the overall safety of the molecule for the assigned section, potentially acting as a core member of the Safety Management Team (SMT), and collaborating with Patient Safety colleagues on program safety reporting.
  • Assisting the Clinical Development Head (CDH) by providing medical input for Clinical Development Plan (CDP), Integrated Development Plan (IDP), and Clinical Trial Protocol (CTP) reviews, and contributing to the development of clinical standards for new disease areas.
  • Acting as a medical expert to support the (Sr.) GPCH or CDH in interactions with internal and external stakeholders and decision boards.
  • Collaborating with the Novartis Institute of Biomedical Research (NIBR) to manage the transition of pre-Proof of Concept (PoC) projects to Development Decision Point (DDP) and working with Business Development & Licensing (BD&L) on target identification and due diligence as needed.

Minimum Requirements:

  • MD or equivalent medical degree required, along with advanced knowledge and clinical training in the medical/scientific area; clinical practice experience of at least 4 years (including residency) and board certification or eligibility in the relevant disease area is preferred.
  • A minimum of 10 years of experience in clinical research or drug development.
  • Experience spanning clinical activities in Phases I through IV, required; 2 years of demonstrated accomplishments in all aspects of conducting clinical trials (planning, executing, reporting, and publishing) in a global/matrix pharmaceutical environment.
  • Working knowledge of the disease area is required, with proven ability to interpret, discuss, and present efficacy and safety data related to clinical trials, as well as the ability to understand and interpret basic and clinical scientific research reports.
  • Demonstrated ability to establish effective scientific partnerships with key stakeholders.
  • Working knowledge of Good Clinical Practice (GCP), clinical trial design, statistics, and regulatory and clinical development processes.
  • Previous global people management experience is preferred, including management in a matrix environment.

Novartis is committed to building an outstanding, inclusive work environment and creating diverse teams that represent the patients and communities we serve.

Accessibility and Accommodation: Novartis is dedicated to providing reasonable accommodations to all individuals. If you require assistance due to a medical condition or disability during the recruitment process or would like to know more about the essential functions of a position, please reach out via email to , including your request's nature and your contact details. Please be sure to mention the job requisition number in your message.

Why Novartis

Helping those affected by disease and their families demands more than innovative science; it requires a community of intelligent, passionate individuals like you. By collaborating, supporting, and inspiring one another, we can achieve breakthroughs that transform patients' lives. Are you ready to create a brighter future together?

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Benefits and Rewards

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How to Apply

Apply online using the form below. Please note that only applications matching the job profile will be considered.

Company Information

Division: Development

Business Unit: Innovative Medicines

Location: Switzerland

Site: Basel (City)

Company / Legal Entity: C028 (FCRS = CH028) Novartis Pharma AG

Alternative Locations: Barcelona, Gran Vía, Spain; Dublin (NOCC), Ireland; London (The Westworks), United Kingdom

Functional Area: Research & Development

Job Type: Full time

Employment Type: Regular

Shift Work: No

Location : BASEL
Country : Switzerland

Application Form

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