Medical Information Specialist

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 Medical Information Specialist role, will make an impact :

Role Purpose

Medical Information Specialist is responsible for providing technical and scientific support for responding to unsolicited inquiries. A key activity is researching, creating and updating Global Scientific Response Documents to answer unsolicited medical inquiries. The role may also involve management of escalated inquiries, peer review of other colleagues’ work, providing literature services and participating in global medical information projects and initiatives. The role has Global scope of responsibilities, requiring membership of Global teams and regular interaction with Global colleagues.

Key Responsibilities

Creates, maintains and reviews Global Scientific Response Documents (GSRDs) and other related content in different formats by ensuring that responses are medically and scientifically accurate, timely, fair balanced and meet customers’ needs. Effectively manages relationships with global colleagues to facilitate timely authoring and review.

Supervisory / Management Responsibilities

No direct supervision, provides direction to others

Position Accountability Scope

Global

Qualification and Experience

Educated to Scientific or Medical degree level or equivalent

Ability to conduct an in-depth analysis of published and unpublished data and engage cross-functional colleagues to identify appropriate resources to utilize in addressing complex medical information inquiries

Have hands on medical Information and Medical Writing experience (3+ years)

Experience or background in working within the pharmaceutical industry, awareness of compliance issues and guidelines around medical information (3+ years)

Understanding of and adherence to regulatory policies governing scientific interactions with HCPs and patients (2+ years)

Experience with GxP requirements and reporting of adverse events with a general understanding of world-wide requirements for MI and PV (2+ years)

Experience with data management (CRM / CMS platforms) and informatics / analytics (3+ years)

Bachelor’s Degree in Pharmacy / Medical / Life Sciences or related field required. Higher degree (e.g. Masters, PhD degree) preferred

English proficiency required for this role : Advanced