Clinical Development Medical Director - Cardiovascular
Clinical Development Medical Director - Cardiovascular
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$ 236600 - 439400
1 Vacancy
Job Description
Job Description Summary
Were a team of dedicated and smart people united by a drive to achieve togetherAre you passionate about shaping the future of clinical development and making a meaningful impact in Cardiovascular medicine
We are looking for an experienced and visionary Clinical Development Medical Director (CDMD) to take the lead in driving the strategic planning and execution of our cutting-edge clinical programs with a focus on anticoagulation.
In this pivotal role you will oversee the end-to-end clinical development process for assigned programs within the Cardiovascular Therapeutic Area. Your expertise and leadership will ensure the seamless execution of clinical development plans while fostering a culture of empowerment agility and collaboration within a dynamic matrixed environment.
If you thrive in a fast-paced purpose-driven organization and have the skills to adapt swiftly to evolving business needs we would love to have you on board!
Job Description
Major Accountabilities
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 (Senior) 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) and GPCH 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 (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards
.
Required Experience
Essential
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) and board certification or eligibility in disease area preferred
Extensive experience in clinical research or drug development
Experience in an academic clinical research or industry environment spanning clinical activities in Phases I through IV required.
Experience of contributing 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 disease area is required with proven ability to interpret discuss and present efficacy and safety data relating to clinical trial(s) and proven ability to understand and interpret basic and clinical scientific research reports
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.
The salary for this position is expected to range between $236400 and $439600 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 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.
EEO 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
$236600.00 - $439400.00Skills Desired
Clinical Trials Cross-Functional Teams Data Analysis Data Monitoring Drug Development Drug Discovery Medical Research Medical Strategy People ManagementRequired Experience:
Director
Employment Type
Full-Time
