US Medical Science Liaison - Northeast

Mylan Specialty L.P.

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via: 

• Access – Providing high quality trusted medicines regardless of geography or circumstance;

• Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and 

• Partnership – Leveraging our collective expertise to connect people to products and services. 

Every day, we rise to the challenge to make a difference and here’s how the US Medical Science Liaison (MSL)-Northeast will make an impact:

Key responsibilities for this role include:

• The Northeast territory includes ME, CT, NY, NJ, PA, DE, DC, VA.

• 100% compliant with all Company policies & procedures.

• Successfully achieve challenging, aligned short- and long-term team and individual performance goals (including Individual Development Plan).

• Engage in non-promotional, truthful, evidenced-based, and non-misleading communications with KOLs/HCPs using educational materials approved by the Medical Review Committee (MRC).

• Respond with Reactive Medical Communications to Unsolicited Medical Requests (UMRs) received from HCPs or other external stakeholders.

• Identify & communicate internally the unmet medical education needs of KOLs/HCPs.

• Develop & communicate internally independent Ad Board, Congress & Customer Insight Reports.

• Staff independent Medical Affairs booths at congresses/conventions.

• Provide investigator and investigator site recommendations for clinical studies.

• Clinical late-stage development activities.

• Engaging Principal Investigators (PIs) for increasing patient recruitment and investigator meetings.

• Site and investigator identification: build new site/investigator relationships.

• Site visits: establish regular cadence for conducting site visits; build relationships with trial site management and wider prescribing community during site visits; ensure co-creation of solutions with PIs for recruitment roadblocks.

• Meetings with investigators: participate in and lead scientific discussions at investigator meetings; actively organize roundtables, ad-boards, and SteerCos outside of trial sites; insight generation - e.g., safety and medical benefit, patient challenges used to refine trial and/or develop solutions.

• Increasing patient recruitment through engagement of Patient Advocacy Groups (PAGs).

• .Engaging PAGs to incorporate patient voice into clinical trials: include PAGs in SteerCos, investigator meetings, ad-boards, roundtables to ensure inclusion of patient perspectives in discussions; recruit patients via PAGs for patient ad-boards to understand unmet need and inform clinical trial decisions e.g., dosing, mode of administration etc., from PhI onwards; incorporate retrospective feedback from patients into clinical trial design.

• Engage PAGs to identify and inform patients of clinical trials: develop patient education materials, e.g., trial information in a patient-friendly format, for PAGs to leverage and sponsor disease awareness programs; engage PAGs if patient recruitment is lagging.

• Medical Congress presence.

• Set-up Medical Affairs booths: leverage digital tools such as interactive media screens to advertise the booth and display publicly available clinical trial information; engage in effective discussions on all clinical and medical topics.

• Pro-actively engage KOLs: engage KOLs as panelists during congresses on behalf of Viatris; engage KOLs/PIs to present clinical trial data at congresses; conduct ad-boards on topics of relevance, e.g., disease management, unmet need.

• RWE & HEOR generation

• Conducting RWE/HEOR studies: ensure diverse patient populations and broader health equity considerations are represented in HEOR/RWE generation studies

• Perform other duties assigned.

The minimum qualifications for this role are:

• Minimum of 5 years of experience in the pharmaceutical, biotech or clinical (e.g. hospital setting/patient care) industry. Medical degree (MD) required. Experience in Cardiology / Rheumatology/ Internal Medicine required. However, a combination of experience and/or education will be taken into consideration. 

• Must possess knowledge of the Medical Science Liaison (MSL) roles and responsibilities, clinical trials, relevant therapeutic areas, u