Medical Director GRITCH
Pubblicato il 09-10-2026 - Medicina in Roma
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The Medical Director has a direct reporting line to the Country Manager.
Its main function is to ensure that all scientific and clinical activities comply with current regulations and support the company’s strategic development.
The Medical Director plays a key role in facilitating communication between the scientific and corporate worlds. Medical Director collaborates with research teams, interprets the results of clinical trials and contributes to defining the therapeutic indications for medicines. Furthermore, he or she supervises scientific publications and attends international conferences and meetings, representing the company within the medical and scientific community.
The Medical Director is expected to comply with all Accord Healthcare Processes and any relevant National guidelines*.
*The European Federation of Pharmaceutical Industries and Associations (EFPIA) Code of Practice, as well as the EU Directive 2001/83/EC and Members' national codes and local regulations,
guide the interactions between the pharmaceutical industry/ Medical Director and HCPs/Patients Association.
The Role
To lead, organise and manage the medical department to ensure the implementation of the company’s strategy.
Develop and execute the local Medical Plan strategy in alignment with global strategies.
Manage the planning and execution of medical activities and programs, including investigator-initiated studies, real-world evidence generation, advisory boards, and scientific exchange events
Responsibility for the clinical development programs
coordinate and facilitate unsolicited Investigator Initiated Trials (IIT) requests, presentation, and publication, in alignment with Medical Affairs’ objectives;
support the Accord Healthcare/ICTAS Sponsored Studies (Phase I to IV) operations when appropriate;
identify and drive opportunities to generate real‑world‑evidence data.
Competitive intelligence on clinical aspects on molecules in the mark