Head, Global Psychiatry Pipeline, Medical Affairs (Senior DirectorExecutive Medical Director)
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Job Location:
Florham Park, NJ - USA
Monthly Salary:
Not Disclosed
Posted on:
14 hours ago
Vacancies:
1 Vacancy
Job Summary
The Medical Affairs organization provides patients healthcare providers and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie products safely and effectively throughout the product lifecycle and the patients journey.
Purpose: Reporting to the Global Head of Neuroscience and Eye Care Pipeline this role provides strategic medical and scientific leadership for core medical affairs activities in AbbVies Psychiatry Pipeline Portfolio. This includes healthcare provider engagement strategies critical data generation educational initiatives and patient safety. Key to success is partnering closely with commercial teams to influence product strategies support market access and drive scientific communications. Offers medical insights and executes data generation expert engagement and communication initiatives across early and late-stage development. Leads gap assessments develops scientific communication platforms and wholistic value narrative (including clinical societal & humanistic) and guides integrated evidence plans to enable launch readiness.
This position can be based from our Florham Park NJ or Mettawa IL sites and will follow a hybrid schedule of 3 days/week onsite.
Responsibilities:
- Lead oversee and support assigned indications and projects in collaboration with cross-functional teams (Medical Clinical Development Commercial Market Access HEOR).
- Initiate and manage medical affairs activities data generation and dissemination to advance scientific and business objectives.
- Provide scientific and technical support for assets deliver presentations maintain relationships with key opinion leaders and contribute to cross-functional teams.
- Guide development of Target Product Profiles (TPP) contribute to Phase II-III trial design and lead Phase 3b/4 strategies in alignment with TPP.
- Lead the planning and execution of advisory boards scientific and medical education programs for both internal and external stakeholders.
- Stay current on scientific advancements and literature; act as a resource for Psychiatry and other relevant therapeutic areas. Initiate and publish research projects.
- Lead cross-functional teams on discrete projects such as data analysis expert engagement publications and collaborations.
- Represent Medical Affairs in due diligence activities for asset acquisitions aligned with disease area strategy.
- Ensure scientific initiatives meet budget timeline and compliance requirements.
- Manages a team of high performing colleagues.
Qualifications :
- Advanced degree (PhD/PharmD/DVM); post-doctoral experience preferred.
- Minimum 10 years experience in clinical trials or medical affairs (pharmaceutical industry or academia); typically 15 years overall experience. Candidates holding an MD may substitute for some years of experience.
- Strong leadership and cross-functional team management skills in a global environment.
- Expertise in a relevant therapeutic area with ability to provide scientific strategy and support.
- Proven ability to independently lead clinical studies or medical affairs teams.
- Knowledge of clinical trial methodology regulatory requirements and protocol design.
- Excellent oral and written communication skills in English.
- People management experience preferred.
Additional Information :
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Key Skills
- EMR Systems
- Post Residency Experience
- Occupational Health Experience
- Clinical Research
- Managed Care
- Primary Care Experience
- Medical Management
- Utilization Management
- Clinical Development
- Clinical Trials
- Leadership Experience
- Medicare
About Company
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more
