Clinical Development Director - CV

Novartis Farmacéutica; Basel-Stadt; Vor Ort; CHF 150’000 - 200’000; Vollzeit

Zusammenfassung

A leading company in the pharmaceutical industry is seeking a Clinical Development Director to lead strategic clinical programs within the Cardio Renal & Metabolic Development Unit. This strategic role requires strong leadership, extensive experience in clinical research, and the ability to work in a global organization, contributing to the advancement of innovative therapies.

Qualifikationen

• At least 7 years of experience in clinical research or drug development.
• Strong understanding of GCP and statistics.

Aufgaben

• Provide clinical leadership and strategic input for clinical deliverables.
• Oversee medical and scientific review of clinical trial data.
• Support interactions with stakeholders as a clinical expert.

Kenntnisse

Communication

Cross-functional collaboration

Clinical research

Clinical trial design

Regulatory processes knowledge

Ausbildung

Advanced degree in life sciences/healthcare (PharmD or PhD preferred)

Jobbeschreibung

The Clinical Development Director (CDD) in the Cardio Renal & Metabolic (CRM) Development Unit is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As a CDD in the CV TA, you will oversee clinical development for the assigned programs and drive the execution of the clinical development plan. You will enable an empowered organization capable of navigating a matrix environment and adapting quickly to business needs.

About the Role

Major accountabilities:

1. Providing clinical leadership and strategic input for all clinical deliverables in the assigned project or section of a clinical program, including clinical sections of protocols, clinical data review, standards, regulatory documents, and publications.
2. Leading development of clinical sections of trial and program-level regulatory documents.
3. Driving execution of the clinical program section in partnership with global line functions, Global Trial Directors (GTDs), and regional/country medical associates.
4. Overseeing ongoing medical and scientific review of clinical trial data with Clinical Scientific Experts, under Medical Lead oversight.
5. Supporting (Senior) GPCH in ensuring overall safety of the molecule; may be a core member of the Safety Management Team.
6. Supporting interactions with external and internal stakeholders and decision boards as a clinical expert.
7. Contributing to scientific training on the disease area and compound; may serve as speaker or Program Manager for other associates.

Qualifications:

• Advanced degree in life sciences/healthcare (PharmD or PhD preferred).
• Minimum of 7 years experience in clinical research or drug development.
• Knowledge of the disease area, clinical trial design, GCP, statistics, and regulatory processes.
• Strong communication skills and ability to work in a cross-functional, global organization.

Why Novartis: Our purpose is to reimagine medicine to improve and extend lives. Join us to be part of this mission. Learn more: https://www.novartis.com/about/strategy/people-and-culture

We are committed to an inclusive, diverse work environment that reflects the patients and communities we serve.

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