Medical Director GRITCH

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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 market and in development

Responsible for the internal cross‑functional collaborations as a scientific partner

Collaborate with commercial staff (Marketing, Sales or NPL team) providing scientific expertise and training to commercial staff as required, reviewing and approving promotional materials in accordance with the local SOP and local law;

attend the local brand teams;

support Market Access supporting the P&R Dossier finalization, hospital formulary submissions and upon request to present the scientific data on Accord Healthcare products;

Support Regulatory

Acts as a clinical interface and actively solicits Key Opinion Leader (KOL) interactions related to the molecule and disease area

Conduct fair and balanced scientific exchanges with KOL to explore mutual clinical and scientific interests, insights generation, scientific/educational meetings (congresses, symposia, etc.), potential research collaborations;

identify opportunities for collaboration with when aligned with Accord Healthcare strategy;

develop and enhance scientific and educational collaborations with Health Care Professionals (HCPs) within the Healthcare community and act as a medical contact for KOL and external medical experts.

Support the launch and lifecycle management of Accord’s product portfolio by delivering relevant medical education, data generation, medical insights, and effective collaboration with global teams.

Review and approval of promotional and non-promotional materials, ensuring the respect of the medical and regulatory standards.

Interaction at Corporate level

The Person

Experience in delivery of scientific presentations and development of relationships with Thought Leaders is strongly preferred,

Ideally, knowledge in data analysis and statistics for purpose of…