Scientific Director Medical Director, Pipeline Medical Strategy – Psychiatry
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Job Location:
Cambridge, MA - USA
Monthly Salary:
Not Disclosed
Posted on:
3 hours ago
Vacancies:
1 Vacancy
Job Summary
The Director Medical Affairs Health Impact (MHI) is a key scientific expert within the Pipeline Psychiatry Therapeutic Area. The position supports the development and execution of the Pipeline Psychiatry medical strategy by leading execution of strategic insight and educational initiatives in psychiatry. The Director provides expert-level scientific strategic and operational input into core MHI activities and cross-functional strategic teams including evidence insight thought leader engagement plans and clinical trial site interactions; generation and dissemination of clinical and scientific data; provider and payer educational initiatives.
This position can be based from our Mettawa IL or Florham Park NJ or Cambridge MA location.
Key Responsibilities
- Collaborates with Pipeline Medical Strategy team to contribute to scientific strategy for pipeline psychiatry assets including asset education and evidence strategies
- Develops and leads the execution of medical education tactics advisory boards and thought leader engagement plan in line with psychiatry pipeline strategic plan.
- Leads conference planning and execution
- Oversee clinical trial site identification engagement and education initiatives
- Provides subject matter expertise for MSL health outcomes and commercial teams including competitive assessments and regular scientific literature reviews.
- Oversees development of early Scientific Communication Platforms and ensures alignment of all tactical initiatives
- Responsible for managing budget for assigned projects including consulting and vendor management.
Qualifications :
- Scientific degree (bachelors) required. MD PhD PharmD and/or other advanced scientific degree strongly preferred. Preferably board certified specialty qualification or equivalent and pharmaceutical industry recognized qualification e.g. MSc
- 5-7 years of prior biopharmaceutical/medical device industry experience including substantial understanding of relevant therapeutic area required
- Prior Medical Affairs experience required
Essential Skills and Abilities
- Should have a good understanding of legal and regulatory guidelines (e.g. knowledge of OPDP promotional regulations CDER/CBER regulations as they relate to drug approvals).
- Good understanding of Good Clinical Practices ICH guidelines PhRMA code FDA CFR ISO clinical research ethics HIPAA and patient privacy laws EU Directive and other applicable local regulations
- Good understanding of Medical Affairs principles study design and publications.
- Knowledge of clinical trial methodology regulatory requirements governing clinical trials and experience in the design of protocols preferred.
- Interactions normally require the ability to gain cooperation of others conduct presentations of technical information concerning specific projects and schedules etc.
- Represents AbbVie at external meetings including investigator meetings scientific association meetings etc.
- Ability to work effectively in a team/matrix environment
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.
This job is eligible to participate in our long-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
