PCP Pharmaceutical Industry & Education Fellow: Incyte - Global Publications

Position Title:

PCP Pharmaceutical Industry & Education Fellow:
Incyte
- Global Publications (1 year)

Time Type:
Full time

Position Summary and

Qualifications:

This is a 1-year post‑graduate training program designed to provide PharmD graduates with in‑depth training and hands‑on experience in the strategic planning, development, and execution of scientific publications within a global pharmaceutical environment. Fellows will work closely with the Global Publications team and cross‑functional partners to support the dissemination of Incyte's scientific data through peer‑reviewed journals, congress presentations, and other scientific communication channels.

This fellowship prepares individuals to pursue a career in the pharmaceutical industry.

Weekly responsibilities are split between Saint Joseph's University (20%) and Incyte (80%).

The fellow will successfully complete projects related to industry, the fellowship program, and teaching responsibilities.

It is expected that as the fellow progresses through the program, the individual will be able to practice with increasing levels of independence.

• Develop and cultivate core skills and competencies in analytical reasoning, critical and strategic thinking, problem solving, communication, influencing, and teamwork.
• Develop professional responsibility and enhance leadership presence.
• Enhance interpersonal communications with healthcare providers, strategic business partners, and consumers.
• Strengthen ability to critically evaluate, interpret, synthesize, and communicate scientific information.
• Instill knowledge of laws, compliance regulations, and guidance's pertaining to medical and regulatory affairs
• Advance critical thinking skills through industry-based projects and cross‑functional teamwork.
• Strengthen leadership and professionalism through participation in academic and industry initiatives.
• Apply and communicate clinical knowledge to projects and project teams.

Industry-based Responsibilities:

• Gain comprehensive understanding of the global publications process including planning, development, review, and execution of scientific publications in alignment with industry standards and compliance requirements.
• Develop skills in scientific writing/editing, data interpretation, and project management by contributing to the management and preparation of abstracts, posters, presentations and manuscripts for key congresses and peer‑reviewed journals.
• Collaborate with cross‑functional teams including Medical Affairs, Clinical Development, Biostatistics, Regulatory, and Commercial to ensure accuracy, consistency, and strategic alignment of scientific communications.
• Engage with external stakeholders including authors, key opinion leaders, and publication vendors to facilitate timely and high quality publication deliverables.
• Understand and apply Good Publication Practice (GPP) guidelines and other relevant policies to ensure ethical and transparent communication of scientific data.

• Support publication leads in the development and execution of global publication plans for assigned therapeutic areas and products.
• Assist in the review of scientific abstracts, posters, oral presentations, and manuscripts.
• Participate in cross‑functional publication team meetings and contribute to strategic discussions regarding data dissemination.
• Coordinate with internal and external authors, medical writers, and publication agency team members to ensure timely delivery of publication projects within budget.
• Track and manage publication timelines, deliverables, and compliance documentation using publication management tools.
• Conduct literature reviews and competitive…