dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.). Key Responsibilities: Ensure products. Identify investigators appropriate for clinical trials. Act as a conduit for unsolicited, investigator-initiated initiation, oversight and follow up of assigned clinical studies and medical projects initiated within therapeutic area of the company (e.g. post marketing clinical activities such as registry/database projects physicians (individually or in groups meetings, clinical sessions, RTDs etc.), where requested. Participate