Director, Content Development

Position Summary

Primary Responsibilities

• Responsible for overseeing and contributing to development of medical content for scientific exchange (e.g. slide decks medical booth content digital enhancements).
• Collaborates with key stakeholders to develop medical content management plans.
• Responsible for review of corporate affairs investor relations commercial and medical materials for scientific accuracy.
• Coordinates with Medical Affairs colleagues vendors and/or outsourced providers in the development review and approval of medical materials; provides medical guidance and expertise to MLR and MRC teams in the review of promotional and medical materials during MLR/MRC meetings.
• Independently evaluates literature interprets complex data writes effectively articulates information to a variety of audiences and effectively negotiates with counterparts from cross-functional areas.
• Effectively prioritizing and allocating resources and developing a culture of excellence and efficient teamwork.
• Maintains expert understanding of product knowledge and labeling associated disease states relevant literature treatment guidelines competitor information and brand strategies and tactics for the therapeutic area involved.
• Communicates and collaborates effectively with other functional groups to cultivate a positive relationship.
• Acts as a subject matter expert to internal customers or appropriate stakeholders to provide them with timely up-to-date scientific and clinical information necessary to make impactful business decisions. Serves as subject matter expert on both general and specific Medical Review practices and provides executable recommendations to senior stakeholders as needed.
• Anticipates risk and implements strategies to avoid potential problems. When appropriate elevates to supervisor and other appropriate functional leaders as needed.
• Other responsibilities as assigned.

Education/Experience/Skills

• PharmD PhD or MD in a scientific discipline or related field required
• 7 years of Medical Affairs experience within the pharmaceutical or biotechnology industry
• 5 years of experience in Scientific Communications Medical Information or related medical content functions
• Experience developing medical content to support scientific exchange activities
• Experience participating in Medical Legal and Regulatory (MLR) and Medical Review Committee (MRC) review processes
• Experience conducting literature searches critically evaluating scientific literature and applying drug information principles
• Strong analytical skills with the ability to interpret scientific data and translate findings into clear medically accurate communications
• Knowledge of the pharmaceutical industrys legal regulatory and compliance environment

Physical Requirements

This role involves regular standing walking sitting and the use of hands for handling or operating equipment. The employee may also need to reach climb balance stoop kneel crouch and maintain visual verbal and auditory communication in a standard office environment and while working independently from remote locations. The employee must occasionally lift and/or move up to 20 pounds. This position requires the ability to travel independently overnight and/or work after hours as required by travel schedules or business needs.

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