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 investigator-initiated research proposals by facilitation proposal, approval, completion, presentation, 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
Disabling Injuries and Product DPMs. Implement / facilitate Generic and Core Competency training and coaching