Assoc Reg Dir Med Aff, Women’s Cancers Job

Date: Jan 8, 2019

Location: Singapore, SG

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Requisition ID: MED004190

Position Overview – Basic Functions & Responsibility
The Regional Associate Director Medical Affairs (RADMA) is responsible for driving execution of scientific & medical affairs plans for their assigned Therapy Areas (TA) in the countries of their assigned region. They will work with the RDMA to support 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. preference to reside in Singapore or co-located country affiliate) in Global Medical Affairs.

Primary activities
• Guides country research division OGMA staff to execute the annual scientific & medical plan for their assigned TA.
• Supports the Regional Medical Affairs Team to ensure execution of agreed medical tactics and leverage best practices. Supports RDMA in executing regional medical affair team meetings.
• Ensures scientific exchange is aligned with the global scientific communications platform
• With Direction from the RDMA, 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 scientific leaders 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  questions 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
• Supports RDMA in reviewing investigator-initiated study proposals prior to headquarters submission (ex-USA)
• Supports RDMA in identifying and communicating regional content and training requirements
• Manages regional programs (patient support, educational or risk management) to support appropriate and safe utilization of MSD medicines
Qualifications

Skills:
Required
• MD. PhD or PharmD/MPharm and recognized medical expertise
• Experience in country / region Medical Affairs
• Strong prioritization and decision-making skills
• 2+ years pharmaceutical (or related) industry experience in the affiliate arena
• In a matrix environment, able to effectively collaborate with partners across divisions
• Excellent interpersonal, analytical, communication (written as well as oral), in addition to results-oriented project management skills
• Scientific leadership and other key stakeholders (payers, public groups, government officials, medical professional organizations) in the assigned therapeutic area


Job: Medical Affairs Generic ONC
Other Locations:
Employee Status: Regular
Travel:
Number of Openings: 1
Shift (if applicable):
Hazardous Materials:
Company Trade Name: MSD


Job Segment: Medical, Pharmaceutical, Risk Management, Project Manager, Healthcare, Science, Finance, Research, Technology

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