Senior Clinical Development Medical Director, Oncology Nuclear Medicine (MD)
Senior Clinical Development Medical Director, Oncology Nuclear Medicine (MD)
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$ 236600 - 439400
1 Vacancy
Job Description
Job Description Summary
Onsite#LI-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.
Job Description
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
Support 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 residency) preferred.
Minimum of 7 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-4 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 preferred 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 $236600 and $439400 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 -based eligible employees will receive a comprehensive benefits package that includes health life and disability benefits a 401(k) with company contribution and match and a variety of other addition employees are eligible for a generous time off package including vacation personal days holidays and other leaves. To learn more about the culture rewards and benefits we offer our people click here.
Why Novartis:
Our purpose is to reimagine medicine to improve and extend peoples 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! Learn more here: receive:
You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities join the Novartis Network here: Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment hiring training promotion or other employment practices for reasons of race color religion sex national origin age sexual orientation gender identity or expression marital or veteran status disability or any other legally protected status.
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 disability you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position please send an e-mail to or call 1 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Salary Range
$204400.00 - $379600.00Skills Desired
Budget Management Clinical Research Clinical Trials Coaching Cross-Functional Teams Lifesciences People Management Risk Management Risk MonitoringRequired Experience:
Director
Employment Type
Full-Time
