Our client is a major, research based pharmaceutical company, one of the industry leaders. Its business employs around 99,000 people in over 100 countries.
As part of a company continuous expansion and development in the Czech Republic we are looking for dynamic, energetic and goal-oriented individual, to be a part of our professional medical affairs team to as well as part of our further company development.
Job Purpose and Key Responsibilities
- Build company position among KOLs, KDMs & HCPs as having Medical Experts in the therapeutic areas.
- Establish connection with R&D activities & build recognition of the company as partner in clinical research
- Build Medical Expertise in therapeutic area to provide scientific & medical support within LOC
- Guarantee high scientific & ethical standard of all promotional activities.
Accountability
- Cooperation with external customers (KOLs, KDMs, Healthcare professionals) - communication with KOLs & KDMs on high medical standard; aim for at least 30% time spent on external activities - cooperation with key members of Professional Societies and Advisory Boards - consulting medical arguments to support categorization process.
- Cooperation on scientific symposia/workshops & publication activities based on partnership (MA as speaker in areas with a strong need for external education) - build relationships through regular face to face contact with HCP, which may include consulting current therapy guidelines, competitors data, publication activities, medical information
- Cooperation with R&D - active participation at Start-up meetings, Investigator meetings & Closure meetings - regular meetings with Local Study Managers - participation on feasibility studies according to the SOP for Study selection and allocation
- Cooperation with Governmental Affairs & Regulatory -medical data input into categorization request, consulting medical data with KDMs & cooperation with GA to finalize categorization process
- Cooperation with Commercial: -medical input into strategic & communication plans, presentation of the medical data - responsibility for medical data of product campaigns, presentation at Product Days & Cycle Meetings -preparation of medical FAQs, clinical trial summaries - delivering new data from conferences, congresses & other scientific events & published sources - approval of all promotional materials, ensuring high ethical & medical standard - is the owner of specific therapy area Advisory Boards
- Cooperates on KOL management with BM - cooperates with BMs on all marketing activities based on delivery of medical data - consulting medical & ethical issues in the field, informs about clinical trials in country
- Medical update for AMs, consults need of training, helps to solve difficult situation with HCP - provides medical information service within company & externally always under medical governance
- Guidance and cooperation with respective Regional Medical/Scientific Adviser - guidance & cooperation with respective therapeutic area.
- Speciality Manager Cooperation with Training Department: - specialized medical training for reps – Product Books, Certification process, Tests & other training materials, including regular update - legislation and Ethical training for commercial