Medical Information Specialist / PharmD / Hybrid Work (JK118)

Position Details:

Our client, a world-leading Pharmaceutical Company in Titusville, NJ is currently looking for an Medical Information Specialist to join their expanding team.

Job Title: Medical Information Specialist / PharmD / Hybrid Work

Duration: 12 months contract, extendable up to 24 months

Location: Titusville, NJ

Role will be Hybrid (3 days onsite, and 2 days remote)

Note:

The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.

You may participate in the company group medical insurance plan

Job Description:

Notes from the Manager:

• I would like to note that we are specifically looking for candidates with recent and robust medical information experience in the pharmaceutical industry with a strong preference for those who have worked with payer related assets such as AMCP dossiers, compendia, Medicaid testimony etc.
• Candidates who would likely not be a good fit include those with a strict Medical Affairs strategy or Regulatory or R&D background and limited or not relevant medical writing experience.

Description:

• Medical Writer Leads the development and timely dissemination of tailored, evidence-based scientific materials for assigned therapeutic area products.
• 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
• Support interactions with drug compendia and collaborates with AD, Med Info PHS and business partners to evaluate strategies for compendia interactions.
• Ensures optimized delivery of high-quality and efficient Payer scientific content and materials by vendors, provides real-time feedback and first line scientific review of materials as needed.
• Voice of Customer and Metrics – 20%
• Leverage voice of customer and other sources of customer information and identify actionable items to enhance development of Payer and Health Systems materials. 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.

Qualifications Education:

• MS or equivalent in Pharmacy or related science field required. Advanced Degree (e.g., PharmD) or PhD is preferred.

Experience: Required:

• A minimum of 2-4 years' experience in Medical Information or Health Economics and Outcomes Research or specialized postdoctoral training in Medical Information or Health Economics and Outcomes Research
• Expertise in the healthcare industry, clinical knowledge or practice across multiple therapeutic areas
• Excellence in leadership skills, collaboration in a matrix environment, influencing and communication (both written and presentation) is required.
• Expertise working in a matrix environment with cross functional teams required.
• Customer Focus – drives excellent customer service and exhibits understanding of healthcare landscape.
• This position may require up to 10% domestic travel for conference attendance and company meetings.

Preferred:

• Working knowledge of United States health care systems and payers - specifically understanding business models and perspectives of managed care and public sector

Top Three Skills:

• Medical Writing, Communication, Collaboration