Therapy Area Lead - Immunology

Job Description

The Therapy Area Lead (TAL) is responsible for developing and executing medical affairs plans related to their assigned therapy areas (TA) in PACE/SEE/Baltics Cluster.

TAL is as well expected to be impactful member of regional cluster and countries cross-functional teams.

Strategic Activities

• Planning and implementation of regional/cluster medical activities within the therapy area(s) in PACE/SEE/Baltics countries by:
• Developing Medical Affairs Plan (MAP) for PACE/SEE/Baltics Cluster including relevant strategies related to SMART plan imperatives and reflecting specifics for the cluster (e.g. different standard of care reimbursement timelines etc.)
• Conducting sustained dialogue with PACE/SEE/Baltics scientific community centering on science and the credible exchange of unbiased scientific information and insights collection
• Preparing and executing sponsored educational activities based on defined HCPs needs
• Prioritizing and defining development areas to meet all scientific and medical needs as well as clinical care gaps
• Planning initiation and implementation of Local Data Generations (or other study types initiated locally) including preparation/review of protocols as needed in alignment with product franchise strategy securing Sr. Management Approval
• Implement publication policy for the therapy areas e.g. securing production of review articles
• Actively search for meetings symposia congresses Continuous Medical Education (CME) research grants/fellowships which could bring additional value to the relevant therapy area
• With focus on key SL in PACE/SEE/Baltics countries build relevant SL engagement plans and engage SL in a balanced scientific Interaction
• Plan and execute cluster Advisory Boards
• Provide input to Global Medical Affairs strategy by insights collecting and timely reporting
• Represent PACE/SEE/Baltics Cluster in front of Regional Medical Affairs team (RDMA) and sustain constant cooperation with this function
• In cooperation with GCTO secure input to our companys HQ-sponsored study allocation as well as national company site selection and investigators. Maintain and update information for local study feasibility on continuous basis and provide timely reply to HQ Request for Information for local study feasibility.
• Attract International Global Medical Affairs (GMA) and our Research Lab studies to the countries of the PACE/SEE/Baltics Cluster.
• Closely and actively cooperating in cross-functional cluster countries and regional teams in order to provide scientific input to HH teams strategies and activities (i.e. HTA reimbursement strategy discussions/negotiations with KDM providing insights and scientific data for planning promotional strategy and other).
• Maintain high level of expertise in the therapy area and be recognized externally and internally as the scientific lead for the relevant therapy area.

Required skills

• Proficient understanding of the drug development process and relevant diseases and therapies
• Strongly demonstrating ethics and integrity
• Excellent interpersonal skills related to management of scientific leaders and authorities
• Collaborative problem-solving agile approach within the team
• A proactive can do attitude and passion for the therapeutic areas of interest
• Ability to work effectively in a matrix organization
• Team player and action-oriented matrix networker across different departments and corporate cultures
• Strong leadership behaviors within delivering value for customers including patients by understanding and meeting their needs; act with candor and courage; make rapid disciplined decisions
• Strong stewardship skills
• Excellent presentation skills
• Excellent understanding of core systems tools and metrics
• English on proficiency level

Education & Experience

• The position requires either a Medical Degree (preferred) or a PhD/PharmaD in life science
• Relevant prior experience can replace the above-mentioned degree requirements

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