Our Gi Life Sciences team is actively seeking an EMEA Medical Affairs Coordinator for a pharmaceutical laboratory.
Start date: Immediate
Location: Geneva
Main responsibilities
- Coordinate the management of contracts and agreements related to medical events with external partners, healthcare professionals and speakers. - Organise and ensure the logistics of travel and accommodation for speakers, experts and faculty members. - Lead the review, validation and alignment of presentations and scientific materials in collaboration with partners, speakers and global medical teams. - Contribute to the organisation and smooth running of local and international medical events, congresses and scientific meetings. - Collaborate with regulatory authorities and internal stakeholders to ensure compliant and timely approval of promotional and non-promotional materials. - Ensure the dissemination and communication of clinical study results and scientific data to relevant stakeholders. - Maintain regular interactions with external partners, investigators and healthcare professionals to support project objectives. - Participate in the design and delivery of training on clinical studies, scientific data and medical education initiatives. - Ensure strict compliance with internal policies, current regulations and ethical standards across all activities.
Profile:
- Scientific degree. - Fluent in French and English. - Proven experience in organising medical congresses as well as disseminating and enhancing clinical study results. - Available immediately.
jid9d3466caen jit0727aen jpiy26aen
Start date: Immediate
Location: Geneva
Main responsibilities
- Coordinate the management of contracts and agreements related to medical events with external partners, healthcare professionals and speakers. - Organise and ensure the logistics of travel and accommodation for speakers, experts and faculty members. - Lead the review, validation and alignment of presentations and scientific materials in collaboration with partners, speakers and global medical teams. - Contribute to the organisation and smooth running of local and international medical events, congresses and scientific meetings. - Collaborate with regulatory authorities and internal stakeholders to ensure compliant and timely approval of promotional and non-promotional materials. - Ensure the dissemination and communication of clinical study results and scientific data to relevant stakeholders. - Maintain regular interactions with external partners, investigators and healthcare professionals to support project objectives. - Participate in the design and delivery of training on clinical studies, scientific data and medical education initiatives. - Ensure strict compliance with internal policies, current regulations and ethical standards across all activities.
Profile:
- Scientific degree. - Fluent in French and English. - Proven experience in organising medical congresses as well as disseminating and enhancing clinical study results. - Available immediately.
jid9d3466caen jit0727aen jpiy26aen
