Jobs

Description

Will the worker be primarily working on-site or can the work be performed remotely? On-site at a client location

What hours will the contingent worker be expected to work? 8a-4:30

What would you consider to be the top three non-negotiable skills ?

• Excellence in leadership skills, collaboration in a matrix environment, influencing, ability to work both individually and as a team contributor.
• Excellence in communication (both written and presentation), pharmaceutical industry experience
• Expertise in the healthcare industry, clinical knowledge, or practice across multiple therapeutic areas

Description:

• The Contractor Medical Writer, Medical Information, Payer and Health Systems reports to the Associate Director/Director Med Info-PHS and supports the development and dissemination of Medical Information scientific content and materials to Payers, Healthcare Intermediaries and Health Systems across the assigned client IM portfolio of products.
• Responsible for quantitative and qualitative payer content related success criteria reports and metrics.

Payer Scientific Content and Materials – 70%

• Supports the development and timely dissemination of tailored, evidence-based scientific materials for assigned therapeutic area products.
• Member of the multi-disciplinary team tasked with reviewing and approving of Payer regulated content prior to it being used
• Supports the development of AMCP standard and pre-approval dossiers, Medicaid formulary requests, and custom requests working collaboratively with Medical Affairs and Real-World Value & Evidence (RW V&E) therapeutic area leads.
• Engages in shaping and development of the Payer Digital Assets in collaboration with Med Info CSI/Digital partners.
• Works closely with RW V&E Field, Medical Affairs Therapeutic Area team(s) and Medical Information Scientific Engagement Contact Center to guide creation and delivery of responses to unsolicited Medical Information Requests from Payers and Health Systems
• Supports the development and dissemination of scientific information in support of assigned products to Clinical Decision Resource Organizations (CDRO) in partnership with Medical Information Affairs, RW V&E, SCG, Therapeutic Teams

Projects and Research – 10%

• Participates in ad-hoc projects and activities as assigned by management.
• Conducts benchmark and research on the landscape of Payer, Healthcare Intermediaries, and health systems