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The MSL serves to advance science and standards of care for patients, healthcare providers and payers, and ensure they can access all the practical and clinically relevant information and solutions they need to use Accord Healthcare's Products efficiently and safely.

Medical Science Liaisons (MSL) is key member of the EMENA Medical Operations/Medical Affairs part of Regulatory Affairs department supporting the local Medical Affairs needs.

The MSLs are field-based scientific expert to external and internal stakeholders delivering scientific/non-promotional information exchange and supporting scientific data and insight generation to provide HCPs/Patients solutions regarding all on-market and in-development Accord Healthcare Products, including those that have been in-licensed, or on topics relating to disease states.

They are responsible for developing and implementing needs facing medical strategies and have a primary liaison role to the medical and scientific community.

The MSL must maintain up-to-date knowledge of relevant scientific information.

The MSL works in coordination with the rest of the Medical unit to meet the Medical Affairs objectives.

The MSL 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/MSL and HCPs/Patients Association.





The Role

Establish and foster professional collaborations with the Healthcare community:

- Map the scientific expertise: Identify, complete and update Thought Leaders (TL) database in the disease area in accordance with the Medical Operations and Medical Affairs Therapeutic Areas directives,
- Conduct fair and balanced scientific exchanges with TL to explore mutual clinical and scientific interests, insights generation, scientific/educational meetings (congresses, symposia, etc.), potential research collaborations,
- Identify opportunities for collaboration with TL when aligned with Accord Healthcare strategy,
- Develop and enhance scientific and educational collaborations with HealthCare Professionals (HCPs) within the Healthcare community and act as a medical contact for TL and external medical experts,
- Reactively interact to unsolicited and documented queries/requests for information from HCPs.

Develop and/or implement unbiased and non‐promotional scientific exchange meetings and educational activities:

Provide scientific/educational presentations to HCP:

- Reactively on ACCORD products (on‐label & off‐label indications), or on Accord Healthcare compounds in development,
- Proactively on ACCORD products (on‐label single‐product presentation) but mainly on disease area management,




- Organize or support legitimate scientific exchange meetings,
- Contribute to/implement medical education programs in the field,
- Contribute to the scientific publication program, if required,
- Organize satellite symposia in regional (in‐country) congresses.

Generate and share insight from HCP to nurture Accord Healthcare's strategy:

- Collect, analyse, and report actionable scientific insight from HCP related to disease state, unmet medical needs, local guidelines, therapeutic trends, competitive activities, compounds in development and the broader healthcare environment,
- If appropriate, organise or support Advisory Boards at Regional level (in‐country),
- Attend and report insights from major National and Regional medical congresses,
- Engage and collaborate on specific initiatives with patient organisations in accordance with external/internal global and local guidance's on Interactions with Patient Organisations and individual patients,
- Contribute to the dissemination of the information within the Company where appropriate,
- Report spontaneous adverse events and product‐related quality complaints in accordance to global and local Accord Healthcare SOP and the local law.

Support to clinical development & ISS (data generation):

- Coordinate and facilitate unsolicited Investigator Initiated Trials (IIT) requests from submission until completion, presentation, and publication, in alignment with Medical Affairs' objectives,
- Support the Accord Healthcare/ICTAS Sponsored Studies (Phase I to IV) operations (see attached Annex), when appropriate,
- Identify and drive opportunities to generate real‐world‐evidence data.

Ensure internal c

📌 MSL Central-South Italy (Italia)
🏢 Accord Healthcare
📍 Italia