Principal Scientist, Medical Affairs – RDMA Ophthalmology (US)

Job Description

Role Summary:

• The Regional Director Medical Affairs (RDMA) is responsible for driving execution of scientific & medical affairs plans for their assigned Therapy Areas (TA) in the countries of their assigned region. They are impactful members of regional cross-functional teams, including regional Commercial, Center of Real-World Evidence (CORE), Policy and Market Access. They engage with their network of scientific leaders in their region. This is a regionally based position (i.e. residing in one of the affiliates of the region or regional hub) in Our Company Research Laboratories Global Medical and Scientific Affairs (Research & Development (R&D) GMSA). 

Responsibilities and Primary Activities:

• Guides country R&D GMSA staff to execute the annual scientific & medical plan for their assigned TA

• Chairs the Regional Medical Affairs Team to ensure execution of agreed medical tactics and leverage best practices

• Ensures scientific exchange is aligned with the global scientific communications platform

• Partners with regional Commercial, regional Center of Real-World Evidence (CORE), regional Policy and regional Market Access to drive development and execution of region plans

• Consolidates actionable medical insights from countries in their region

• Engages with a network of contracted Scientific Leaders (SL) and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) from their region

• Supports, as regional TA expert, affiliates staff in engagement with their national scientific leaders

• Organizes regional expert input events to answer Our Company’s questions regarding how to implement new indications: advisory boards and expert input forums

• Organizes regional symposia and educational meetings

• Supports countries with the development of local data generation study concepts and protocols

• Reviews investigator-initiated study proposals prior to headquarters submission (ex-USA)

• Manages regional programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Company’s medicines

Required Qualifications, Skills & Experience:

Minimum:

• MD, PhD, PharmD or OD (MD preferred) and recognized medical expertise in the Retinal therapeutic space

• Five+ years’ experience in country / region Medical Affairs

• Strong prioritization and decision-making skills

• Able to effectively collaborate with partners across divisions in a matrix environment

• Excellent interpersonal, analytical, communication (written as well as oral) skills, in addition to results-oriented project management skills

Preferred:

• Scientific leadership and other key stakeholders (payers, public groups, government officials, medical professional organizations) in the assigned therapeutic area

#eligibleforERP

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US and Puerto Rico Residents Only:

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