Sr. Mgr./Assoc. Director, Content Development & Me

at Incyte Corporation in Wilmington, Delaware, United States

Job Description

Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.
The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules.
Job Summary (Primary function):
The Senior Manager/Associate Director, Content Development and Medical Information is responsible for the identifying needs and development of US Medical Affairs scientific exchange materials for field-based US Medical Affairs staff (i.e., Medical Science Liaisons), medical meeting scientific content, advisory board materials, content for internal staff training, medical congresses and other relevant projects and programs consistent with the Medical Affairs Strategic and Operational Plan. This individual will work cross-functionally to build US Medical Affairs scientific content through collaboration with cross-functional partners in Research, Development, Commercial, Public Affairs, and US and Global Medical Affairs, as well as external experts in the field of Dermatology. The individual will also assist, as needed, in the development of training materials, product dossiers, frequently asked question (FAQ) documents and standard response letters.
Essential Functions of the Job (Key responsibilities):
Develops content for US Medical Affairs programs and projects including agendas, medical presentations, ad hoc clinical engagements, and internal scientific meetings and select medical congresses, and supports cross-functional execution.
Collaborates with cross-functional partners in Research, Development, Commercial, and Medical Affairs, and assists with development of scientific exchange materials for emerging therapeutic areas.
Manages the development and execution of Advisory Boards, including identification and engagement of external experts, development and approval of meeting content, and execution of the advisory board meeting.
Works cross-functionally to develop medical congress scientific booth content related to research targets, investigational agents, and clinical study recruitment.
Develops and maintains expertise in inflammation and autoimmunity therapeutic areas, including disease states, treatment modalities, and ongoing research strategies.
Provides medical literature surveillance and oversight for US Medical Affairs, and identifies and communicates pertinent updates in a timely manner.
Manages US Medical Affairs external vendors, including those involved in scientific content development and advisory board execution, and participates in the review and selection process.
Participates in the creation and maintenance of departmental SOPs necessary to ensure highest levels of quality, compliance, and operational efficiency.
Assists with creation of medical information standard response letters, product dossiers, and frequently asked question (FAQ) documents, as needed.
Qualifications (Minimal acceptable level of education, work experience, and competency):
Advanced scientific or clinical degree in the life sciences (e.g., Pharm.D., or Ph.D); minimum of 2 years' experience working in a Medical Information/Medical Affairs capacity for a pharmaceutical, medical device, medical communications company, or equivalent experience, is required.
Extensive experience creating scientific content, including disease state and product-related slide presentations, is required.
Experience in the management and execution of Advisory Boards is required.
Track record of exhibiting leadership behaviors related to collaborating cross-functionally to build consensus, and executing simultaneous projects in a timely manner, is required.
Knowledge of FDA regulations regarding the dissemination of Medical Information and drug promotion, is required.
Excellent oral and written communication skills are required.
Excellent project management skills, including the ability to plan, prioritize, and execute multiple projects are required.
Experience in inflammation and autoimmunity, especially dermatology, is strongly preferred.
Approximately 15% travel commitments.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list... For full info follow application link.

We appreciate, celebrate, and thrive on one another’s differences and strengths and are proud to be an Equal Opportunity Employer. By valuing diversity of backgrounds and perspectives and prohibiting all forms of harassment, we are able to promote a collaborative and innovative work environment in which everybody can contribute to their fullest potential.        

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Job Posting: 1082713

Posted On: Dec 05, 2022

Updated On: Jan 04, 2023

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