Medical Affairs Specialist EMEA DBS
il y a 4 semaines
Role Overview
We are seeking a highly skilled Medical Affairs Specialist to join our EMEA team, focusing on Deep Brain Stimulation (DBS) technologies. As a key member of our medical affairs team, you will play a crucial role in building and maintaining relationships with Key Opinion Leaders, engaging them on strategic areas of importance to Boston Scientific.
Key Responsibilities
- Data Generation
- Evaluate external clinical research proposals and collaborate with cross-functional teams to advise on how research proposals fit the overall clinical strategy.
- Participate in the development of the EMEA clinical evidence plan, assessing gaps and needs that align with Boston Scientific's strategic focus and drive research topics of interest.
- Provide support for scientific rigor of all regional Boston Scientific funded research.
- Communicate with investigators on all scientific questions prior, during, and after the review process for investigator-sponsored research, research collaborations, and ancillary research grants.
- Stay in close contact with investigators, arranging scientific support and monitoring project progress to provide clear project status during reviews with cross-functional teams.
- Inform relevant Boston Scientific departments who may benefit from results or publications from supported projects.
- Ensure clinical evidence generation supports Boston Scientific's strategic needs regionally, with equitable participation in research from the EMEA region.
- Develop relationships with EMEA Key Opinion Leaders and field personnel through scheduled meetings and other interactions.
- Act as a scientific liaison between commercial and global scientific teams.
- Data Dissemination and Others
- Provide clinical presentations and high-level pipeline presentations in key targeted accounts, collaborating closely with functional partners to develop and execute KOL programs.
- Execute and support physicians in delivering medical educational programs, such as symposia.
- Lead the content and format of EMEA medical symposium/congress presentations, ensuring strategic focus.
- Lead and contribute to content for clinical messaging and medical educational programs.
- Participate in the global clinical evidence plan creation and follow-up with cross-functional partners.
- Lead data dissemination on relevant clinical evidence coming out of EMEA congresses or clinical papers, collaborating with global and country teams.
- Engage identified healthcare professionals and Key Opinion Leaders to demonstrate the clinical outcomes and benefits of Boston Scientific products, technologies, and therapies.
- Lead EMEA advisory boards to collect clinician feedback on product development, clinical, education, and other topics supporting EMEA strategy.
- Procedural
- Communicate with cross-functional teams frequently to align on priorities.
- Be a strong advocate for patient outcomes and investment in research.
- Support internal training initiatives when appropriate.
- Support scientific phrasing of claims in marketing collateral.
Requirements
We are looking for a candidate with strong scientific acumen, excellent presentation and communication skills, and a collaborative approach. The ideal candidate will have:
- A PhD in Neurosciences (or equivalent relevant qualification).
- Specialized knowledge of clinical issues associated with Deep Brain Stimulation.
- Thorough knowledge of clinical research, device development process, regulatory requirements, laws, and good clinical practices.
- Experience in running clinical trials is advantageous.
- Demonstrated ability to develop and maintain relationships with Key Opinion Leaders.
- Demonstrated strength in developing and delivering strong, storytelling presentations.
- Proven ability to communicate complex data to diverse audiences.
- Demonstrated success in managing projects, particularly clinical research programs.
- Fluent in English.
- Willing and able to travel as required by workload (30-50%).
-
Medical Affairs Specialist EMEA DBS
il y a 1 mois
Paris, Île-de-France Boston Scientific Temps pleinJob Title: Medical Affairs Specialist EMEA DBSAt Boston Scientific, we are committed to advancing science for life by developing innovative medical solutions that improve patient lives. We are seeking a highly skilled Medical Affairs Specialist to join our EMEA team, focusing on Deep Brain Stimulation (DBS) technologies.Key Responsibilities:Evaluate external...
-
Medical Affairs Specialist EMEA DBS
il y a 4 semaines
Paris, Île-de-France Boston Scientific Temps pleinJob Summary:We are seeking a highly skilled Medical Affairs Specialist to join our EMEA team, focusing on Deep Brain Stimulation (DBS) technologies. The successful candidate will be responsible for building and maintaining relationships with Key Opinion Leaders, engaging them on strategic areas of importance to Boston Scientific.Key Responsibilities:Evaluate...
-
Medical Affairs Specialist EMEA DBS
il y a 3 semaines
Paris, Île-de-France Boston Scientific Temps pleinKey ResponsibilitiesThe role of the Medical Affairs Specialist will be to build, develop and maintain relationships with Key Opinion Leaders, engaging them on their fields of interest and on areas of strategic importance to Boston Scientific. This includes providing clinical presentations and high-level pipeline presentations in key targeted accounts. The...
-
Global Medical Affairs Specialist
il y a 4 semaines
Paris, Île-de-France Exact Sciences Corporation Temps pleinJob DescriptionExact Sciences is seeking a Global Medical Affairs Specialist to join our team in France. As a Global Medical Affairs Specialist, you will play a critical role in supporting the commercial business and reimbursement objectives for our portfolio of products, including breast and colorectal cancers.You will engage with customers and colleagues...
-
Medical Affairs Specialist
il y a 3 semaines
Paris, Ile-de-France Oxford Global Resources Temps pleinMedical Affairs Consultant (6-month contract, potential for permanent role)Location: France (Part-time, with 1 day in the Paris office)We are looking for an experienced Medical Affairs Consultant to join our client's growing medical team in France. This is a 6-month contract with the possibility of evolving into a permanent role based on future projects...
-
Medical Affairs Consultant
il y a 3 semaines
Paris, Île-de-France Oxford Global Resources Temps pleinWe are seeking a highly skilled Medical Affairs Consultant to join our client’s growing medical team in France. This is a 6-month contract with the possibility of evolving into a permanent role based on future projects and workload.Our client’s Medical Affairs team is currently composed of two members, and they are seeking to expand by integrating a...
-
Medical Specialist Group Surgeon
il y a 4 semaines
Paris, Île-de-France Medical Specialist Group Temps pleinWe are seeking a highly skilled Consultant Surgeon to join our team at the Medical Specialist Group. As a key member of our partnership, you will provide high-quality care to patients and contribute to the development of our services.Our unique healthcare model sets us apart from the NHS, offering a distinct approach to medical care. You will work closely...
-
Regional Medical Affairs Director
il y a 4 semaines
Paris, Île-de-France Insulet Corporation Temps pleinInsulet Corporation is seeking a highly motivated and performance-driven Medical Affairs Senior Manager to join our team. The successful candidate will be responsible for developing and executing the Medical Affairs strategy for a region within International, focusing on existing and new distributor markets.The Medical Affairs Senior Manager will work...
-
Medical Affairs Senior Manager
il y a 4 semaines
Paris, Île-de-France Insulet Corporation Temps pleinInsulet Corporation is seeking a highly motivated and performance-driven Medical Affairs Senior Manager to join our expanding team. The successful candidate will be responsible for developing and executing the Medical Affairs strategy for a region within International, focusing on existing and new distributor markets.The Medical Affairs Senior Manager will...
-
Regulatory Affairs Specialist for Medical Devices
il y a 4 semaines
Paris, Île-de-France ProductLife Group Temps pleinWe are seeking a Regulatory Affairs Specialist for Medical Devices to join our team at ProductLife Group in Paris.ResponsibilitiesDevelop and maintain registration dossiers in accordance with European regulation (2017/745) and other specific requirements.Coordinate with contributors (R&D, Production, QA, Clinical) to ensure dossier constitution meets...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France Alnylam Pharmaceuticals Inc. Temps pleinKey Responsibilities:As a Regulatory Affairs Specialist at Alnylam Pharmaceuticals Inc., you will provide strategic regulatory advice to internal stakeholders regarding tactics and communications related to Alnylam's marketed products, investigational treatments, and disease areas to healthcare providers, patients, payers, and other audiences. You will help...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France ProductLife Group Temps pleinIn the context of a new project, we are seeking a Regulatory Affairs Specialist to join our teams in Paris.ResponsibilitiesDevelop and maintain regulatory dossiers and coordinate with cross-functional teams.Ensure compliance with European regulations (2017/745) and other regional requirements.Maintain technical files and ensure export compliance.Elaborate...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our regulatory team, you will be responsible for ensuring the delivery of regulatory activities performed onsite in the Paris region.About usProductLife Group is a leading company in the pharmaceutical industry, and we are...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France DSM Temps pleinJob Title: Regulatory Affairs SpecialistJob Summary: We are seeking a highly skilled Regulatory Affairs Specialist to join our team at DSM. As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements in the food industry.Key Responsibilities:Support with compliance checks and regulatory assessment of food...
-
Senior Regulatory Affairs Specialist
il y a 3 semaines
Paris, Île-de-France PROJECTUS Temps pleinSenior Regulatory Affairs Specialist - Medical Devices (MDR)We are seeking a seasoned Regulatory Affairs professional to join our team at Projectus Consulting, a renowned brand within the Surgical Device market. As a result of our continued success and remaining at the forefront of pioneering medical device innovation, we require an experienced expert to...
-
Senior Regulatory Affairs Specialist
il y a 1 mois
Paris, Île-de-France CooperCompanies Temps pleinJob Title: Senior Regulatory Affairs SpecialistCooperVision is a leading manufacturer of soft contact lenses with a presence in over 100 countries. We're committed to creating an inclusive and engaging workplace where everyone's contribution counts.About the Role:We're seeking a Senior Regulatory Affairs Specialist to provide regulatory support, guidance,...
-
Regulatory Affairs Specialist
il y a 3 semaines
Paris, Île-de-France ProductLife Group Temps pleinProductLife Group is seeking a highly skilled Regulatory Affairs Officer to join our team in Paris. We are looking for an expert with a strong background in medical devices regulation, particularly in the context of the new European regulation (2017/745) and other specific requirements in various zones.Key ResponsibilitiesDevelop and coordinate the...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a Regulatory Affairs Specialist to ensure the delivery of regulatory activities performed onsite in Paris region as part of a project for one of our Top Clients.About usProductLife GroupResponsibilitiesCoordination of the collection of information relating to regulatory requirements or the analysis of the...
-
Regulatory Affairs Specialist
il y a 4 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs SpecialistWe are seeking a Regulatory Affairs Specialist to ensure the delivery of regulatory activities performed onsite in Paris region.About usProductLife GroupResponsibilitiesUnder the responsibility of the regulatory coordinator of this project and in close collaboration with subsidiaries, production sites, CMC Regulatory Project...
-
Regulatory Affairs Specialist
il y a 3 semaines
Paris, Île-de-France ProductLife Group Temps pleinRegulatory Affairs Specialist We are seeking a Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our regulatory team, you will be responsible for ensuring the delivery of regulatory activities performed onsite in the Paris region. About us: Group 10 Responsibilities: Coordination of the collection of...