Clinical Development Medical Director, Oncology Nuclear Medicine (MD) in , us

Energy Jobline ATTB; Théméricourt; Sur place; EUR 205 000 - 383 000; Plein temps

Résumé du poste

A global pharmaceutical company is seeking a Senior Clinical Development Medical Director to lead the strategic management of clinical programs. The role requires expertise in oncology and clinical research experience of 4+ years. The position offers a salary range between $236,600 and $439,400 per year, with comprehensive benefits and performance incentives. Join us to improve and extend people's lives by leading exciting cancer treatment innovations.

Prestations

Performance-based cash incentive

Comprehensive benefits package

Generous time off package

Qualifications

• 4+ years of clinical practice experience.
• 3+ years of experience in clinical research or drug development.
• 2 years of conducting clinical trials in a matrix environment.

Responsabilités

• Lead strategic planning for clinical programs.
• Drive execution of the clinical development plan.
• Provide clinical leadership and input for regulatory documents.

Connaissances

Clinical research

Oncology knowledge

Scientific partnership

Formation

MD or equivalent medical degree

Description du poste

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We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.

Senior Clinical Development Medical Director

Onsite East Hanover, New Jersey

About the role: As the Senior Clinical Development Medical Director (CDMD), you will lead the strategic planning and management of the assigned clinical program from an end‑to‑end clinical development perspective. As Sr CDMD, you will have oversight of the clinical development for the assigned programs and drive execution of the clinical development plan. You will enable an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. We are striving to develop treatments for Lung, Breast & Prostate Cancers, MDS & AML, CML and sickle‑cell disease, and are pushing the boundaries of innovation with CAR‑T and Radioligand therapies.

Your Key Responsibilities

• Providing clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program
• Leading 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, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable
• Supporting the Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues
• Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas
• As a medical expert, supporting the GPCH or CDH in interactions with external and internal stakeholders and decision boards

Role Requirements

Essential Requirements

• MD or equivalent medical degree is required in addition to advanced knowledge and clinical training in medical/scientific area; Clinical practice experience: 4 years (including ) .
• Minimum of 3 years of experience in clinical research or drug development with expertise in nuclear medicine.
• Experience in an academic or industry environment spanning clinical activities in Phases I‑IV required.
• 2 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry required.
• Working knowledge of Oncology is required, with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trials.
• Demonstrated ability to establish effective scientific partnerships with key stakeholders.
• Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes.
• Previous global people management experience is , though this may include management in a matrix environment.

Desired Requirements

• Board Certification Nuclear Medicine

Novartis Compensation and Benefit Summary

The salary for this position is expected to range between $236,600 and $439,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance‑based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US‑based eligible employees will receive a comprehensive benefits package that includes health, life and benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

Why Novartis

Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us!

Accessibility and Reasonable Accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or , you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an email to [e-mail] or call [phone] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Equal Opportunity Employment

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of , , , , , , , marital or veteran status, , or any other legally protected status.

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