Role Description
The Associate Director, Medical & Scientific Affairs β Acute Care provides medical and scientific strategic and operational input into core medical affairs activities such as:
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Health care professional and provider interactions (Payers, Patients, Prescribers, and Providers)
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Identification of clinical partners and generation of clinical and scientific data
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Communicates study results through reports and forecasts publications/abstracts/posters to stakeholders
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Works closely with commercial teams to provide strategic medical input into core brand (product) strategies
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Supports medical and marketing activities (promotional material generation and product launches) and market access
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Executes core medical affair tactics to support launch
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Collaborates with clinical development on Medical Affairs support of priority trials
This position reports to the Senior Director, Medical & Scientific Affairs β Acute Care and is part of the Medical & Scientific Affairs organization, a team of medical specialists dedicated to all medical aspects of safe and effective therapeutic areas.
This role may be fully remote, working remotely to cover a global business area.
In this role, you will have the opportunity to:
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Perform gap analysis for Integrated Medical Plans; identify opportunities in Integrated Evidence Plans (IEPs) and drive these in Kaizen workshops
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Develop patient journeys / disease maps together with the global franchise teams
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Develop the study strategy; communicate the strategy internally and externally; train the MSL team on study funnel management; execute study strategy (study funnel development; budget)
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Forecast publications / abstracts / posters and identify opportunities to leverage key data for presentations or other collateral with the MSL team and commercial team(s)
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Communicate and translate clinical/scientific insights and research concepts from KOLs into actionable guidance for product development teams
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Contribute to the development of Scientific Advisory Boards
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Author all grants in the acute care disease area and support medical affairs activities including dissemination of data supporting overall product scientific and commercial strategy
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Serve as deputy for Senior Director accountabilities when director is absent
Qualifications
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Advanced Degree: MD/PhD, MD, PhD, or PharmD with 9+ years of experience required
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Residency or additional post doctorate experience preferred
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Substantial understanding of relevant therapeutic area required
Requirements
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Knowledge of clinical trial methodology, regulatory requirements governing clinical trials, and experience in the design of protocols preferred
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Ability to interact externally and internally to support global business strategy
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Must possess excellent oral and written communication skills
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Represents Beckman Coulter at external meetings including investigator meetings, scientific association meetings, etc.
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Ability to interact with and coordinate appropriate scientific and medical activities with internal stakeholders (i.e. commercial, clinical operations, R&D, statistics, regulatory, etc.) as they relate to ongoing medical affairs projects
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Ability to travel a minimum of 20-25% of the time (domestic and international)
Benefits
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Comprehensive package of benefits including paid time off
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Medical/dental/vision insurance
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401(k) to eligible employees
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Bonus/incentive pay eligibility