Select how often (in days) to receive an alert :
The information below covers the role requirements, expected candidate experience, and accompanying qualifications.
To develop and foster professional relationships with Therapeutic Area Experts (TAEs) and a broad range of external stakeholders through effective scientific communication and non-promotional activities in the ultimate benefit of patients.
To bring field insights, then build up into medical strategy / plan and contribute to the brand’s success.
Responsibility
- Maintain the highest level of knowledge regarding products in responsible therapeutic area (TA) and investigational compound information to be a scientifically credible partner of TAEs.
- Proactively identify and develop long term peer-to-peer relationships with TAEs and other relevant stakeholders.
- Establish Servier presence within academic institutions and relevant societies in defined therapeutic areas of strategic interest to the company.
- Ensure appropriate identification and mapping of TAEs
Create and update periodically the TAEs list by utilizing objective, pre-defined criteria to profile opinion leaders.
Execute the medical activities aligned with medical strategies and TAE engagement plan, including but not limited to Advisory board meetings, medical symposiums, Expert exchange meetings, etc.Delivery of medical information to TAEsDisseminate new scientific data to Healthcare professionals (HCP) related to marketed Servier products and be the point of contact for Servier pipeline related communications.
Support scientific training of Servier-contracted speakers by providing education as needed.Provide clinical and medical presentations to external stakeholders upon request and as appropriate.Depending on the situation, may support Promotional Material Review and Approval (PMRA) process along with Medical Information team to maintain the high quality of our scientific communication and to ensure the balanced perspective.Support HCPs for investigator-sponsored study (ISS) as per Servier SOP as well as engaging with GMA team on ISS proposals as appropriate :As the owner of internal process (i.e., Local Coordinator), communicating and facilitating for the local / global review process, initiated by unsolicited request from investigator and monitoring the relevant documents in iENVISION.
As main contact person of Servier to investigator, communicating timely with investigator on IP supply, payment milestone, PV reporting and publication plan.Support the management of clinical studies and medical projects initiated by Servier (SIT) in the Affiliate, ensuring that activities are carried out in accordance with relevant processes and procedures.Ensure a strong medical and scientific presence in key academic centres by facilitating research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest.
Contribute to develop local initiated study concept and protocol based on clinical insights and generate publications in collaboration with TAEs and internal publications team.Support for issue management and communication between clinical operation and investigator.Collaborate with cross-functional teams including but not limited to sales, training, marketing, regulatory affairs, market access, etc., through sharing insights on product, patient and therapeutic area, to ensure that Servier can develop pertinent product strategies.Support cross-functional team with scientific expertise and understanding of the designated therapeutic area, including the training of internal staff as required.
Support developing scientific educational materials and agenda for quality educational programs.Complying with local regulations and Servier policies.Requirement
Graduate degree (Bachelor or Masters) in science, biotechnology or nursing with technical qualifications.Advanced degree (e.g., PharmD, PhD, MD) in a relevant scientific discipline is highly preferred.2. Experience
More than 1 year of field medical or MSL experience, preferably in a multinational company.OR, more than 2 years of related function such as other positions in Medical department, Regulatory, Market Access or Clinical Operations, etc., preferably in a multinational company.Launch experience and / or Oncology Therapeutic area experience is highly preferred.Laboratory / Research experience is a strong plus.Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of the organization.Experience in developing and maintaining expert knowledge for the assigned therapeutic area, and in medical research in general.3. Required skills
Ability to comprehensively learn about new subject areas and environment.Strategic thinking and analytical scientific literacy.Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain professional relationships with multiple stakeholders, in both Korean and in English.Substantial business acumen.Ability to prioritize and handle complex situations and projects.Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity.Leadership, active listening, good interpersonal skills, emotional intelligence and strength of conviction.J-18808-Ljbffr
