Associate Clinical Development Medical Director
Associate Clinical Development Medical Director
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$ 204400 - 379600
1 Vacancy
Job Description
Band
Level 5Job Description Summary
The Associate Clinical Development Medical Director (Assoc. CDMD) is responsible for the scientific and medical strategy of assigned clinical trial(s) medical and scientific monitoring and reporting of quality data. May be responsible for the scientific and medical strategy of assigned sections of a clinical development program depending on the size and complexity.Job Description
MAJOR ACCOUNTABILITIES:
Is a global clinical manager or country / cluster leader responsible for clinical program(s) across indications executing medical strategy for development and marketed products in a defined therapeutic area -Responsible for the scientific and medical strategy of assigned clinical trial(s) medical and scientific monitoring.
May be responsible for the scientific and medical strategy of assigned sections of a clinical development program.
Contributes to the development of clinical sections of trial and program level regulatory documents -Contributes to the execution of the section of the clinical program in partnership with global line functions.
Contributes to ensuring overall safety of the compound for assigned trial(s) in collaboration with Patient Safety.
Supports by contributing medical input into IDP and CTP reviews and contributing/driving development of disease clinical standards for new disease areas -Contributes to medical/scientific training of relevant Novartis stakeholders.
May serve as speaker for franchise medical/scientific training -Contributes to the global initiatives (e.g. process improvement training SOP development other Clinical Development line function initiatives) -Contributes to talent and career development of CD associates through on-boarding coaching and/or mentoring support; -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)
REQUIREMENTS
MD or equivalent medical degree required. Advanced knowledge and clinical training in a medical/scientific area (e.g. internal medicine or sub-specialty) required with Medical Board certification preferred; Clinical practice experience 4 years (including residency) preferred
3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV. 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
Working knowledge of the assigned disease area is desired with proven ability to interpret discuss and present efficacy and safety data relating to clinical trial(s) or program level
Demonstrated ability to establish effective working relationship with key investigators
Working knowledge of GCP clinical trial design statistics and regulatory and clinical development processes
Strong communication skills written and oral
Strong interpersonal skills
Strong negotiation and conflict resolution skills
Proven ability to work independently or in a cross-functional team setting
The salary for this position is expected to range between $204600 and $379400 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 benefits. In 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 gender national origin age sexual orientation gender identity or expression marital or veteran status disability or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.
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 in order to perform the essential functions of a position please send an e-mail to call 1 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Range
Skills Desired
Clinical Trials Data Analysis Data Monitoring Drug Development Drug Discovery Medical Strategy People ManagementRequired Experience:
Director
Employment Type
Full-Time
