Senior Medical Advisor

hace 6 días


Alcobendas, Madrid, España BeiGene A tiempo completo
About the Role

We are seeking a highly motivated and experienced Senior Medical Advisor to join our team at BeiGene. As a key member of our Medical Affairs department, you will play a pivotal role in supporting the development and execution of local medical strategies.

Key Responsibilities
  • Establish and maintain credible peer-to-peer scientific relationships with national and regional key opinion leaders and medical experts.
  • Provide education to the medical community on BeiGene products and disease areas of focus.
  • Work closely with internal stakeholders to develop and execute a medical plan designed to meet shared objectives.
  • Facilitate responses to unsolicited requests for medical information, often in direct collaboration with BeiGene Medical Information Services personnel as appropriate.
  • Develop and execute tactics for communicating complex scientific information to the healthcare community.
  • Provide impactful feedback, information and insights to internal stakeholders on emerging clinical and scientific trends from external interactions to help shape company strategy and research, and to ensure the safe and appropriate use of BeiGene products.
  • Act as a scientific resource with professional and advocacy organizations with the objective of developing relationships and identifying potential collaborative opportunities.
  • Build specific excellence and integrity within the healthcare community. Develop contacts with key clinicians, university teaching hospitals, and other medical/scientific groups and stakeholders.
  • Develop speakers through one-on-one clinical training on approved clinical slide sets.
  • Assist in the development and execution of clinically relevant regional medical meetings (e.g., advisory boards, consultancies, and investigator meetings) as required.
  • Identify and verify investigators and sites for company-sponsored clinical trials. Scientifically support clinical trials and investigator centers for ongoing clinical studies as needed.
  • Serve as the primary territory liaison for the submission and review of Investigator-Research proposals, facilitating the process from concept submission through publication and uncovering scientific data that may have the potential for publication and/or abstract presentation.
  • Support Healthcare Professionals with Expanded Access to individual requests or programs as needed.
  • Provide scientific training and medical support for internal Medical Affairs and Commercial colleagues as needed.
Requirements
  • MD, PharmD., or Ph.D. within a clinical and/or scientific profession (or an equivalent level of professional, clinical, and/or scientific education, training, and experience) preferred.
  • > 5 years of existing experience as a Medical Science Liaison, Medical Advisor, or similar field-based Medical Affairs role within other Biotech/Pharmaceutical companies.
  • Experience in hematology is strongly preferred.
  • Exposure to Clinical Operations and Drug Development is also preferred.
  • Knowledge of applicable treatment, compliance, and regulatory guidelines within the given therapeutic area and country or region.
Competencies
  • Impactful verbal and written communication skills.
  • Ability to effectively disseminate and present complex scientific information in a dynamic and global environment.
  • Strong comprehension of disease states, knowledge of differential algorithms for treatment decisions, and experience in disease states of interest to BeiGene.
  • Understanding of the design and execution of research studies and strategic implications.
  • An expert in understanding the Country's health care delivery system, including the managed care arena and its impact on patient care, local medical care, and the pharmaceutical industry. Ability to identify the unmet medical, educational, and research needs at a local (& regional) level in the medical community.
  • Able to lead training initiatives and best practices.
  • Strong time management and organizational skills.
  • Able to engage in work-related travel.
Computer Skills
  • PC and iPad literacy, proficient in Microsoft Office required.
  • Experienced with electronic CRM systems.
Other Qualifications
  • High Level of English Communication (verbal and written).
  • Valid Drivers License.


  • Alcobendas, Madrid, España Parexel A tiempo completo

    Job SummaryParexel is a leading biopharmaceutical services company that improves the world's health by transforming scientific discoveries into new treatments. We are seeking a highly experienced Senior Medical Director to lead our Safety Medical Sciences business functions and provide strategic inputs to Safety Services Leadership.Key...


  • Alcobendas, Madrid, España Parexel A tiempo completo

    Job SummaryParexel is a leading biopharmaceutical services company that improves the world's health by transforming scientific discoveries into new treatments. We are seeking a highly experienced Senior Medical Director to lead our Safety Medical Sciences business functions and provide strategic inputs to Safety Services Leadership.Key...


  • Alcobendas, Madrid, España Parexel A tiempo completo

    About the RoleParexel is seeking a highly experienced Senior Medical Director to lead our Safety Medical Sciences business functions and provide strategic inputs to Safety Services Leadership. As a key member of our team, you will be responsible for implementing suitable technology and innovations for the function and acting as Business Owner of related...


  • Alcobendas, Madrid, España Parexel A tiempo completo

    About the RoleParexel is seeking a highly experienced Senior Medical Director to lead our Safety Medical Sciences business functions and provide strategic inputs to Safety Services Leadership. As a key member of our team, you will be responsible for implementing suitable technology and innovations for the function and acting as Business Owner of related...


  • Alcobendas, Madrid, España Parexel A tiempo completo

    About the RoleParexel is seeking a highly skilled Medical Director to join our team. As a Medical Director, you will be responsible for providing medical expertise and leadership to our clients across the globe.Key ResponsibilitiesProject Execution: Deliver medical support for successful project delivery, including medical monitoring and pharmacovigilance...


  • Alcobendas, Madrid, España Parexel A tiempo completo

    About the RoleParexel is seeking a highly skilled Medical Director to join our team. As a Medical Director, you will be responsible for providing medical expertise and leadership to our clients across the globe.Key ResponsibilitiesProject Execution: Deliver medical support for successful project delivery, including medical monitoring and pharmacovigilance...


  • Alcobendas, Madrid, España Parexel A tiempo completo

    Job SummaryParexel is seeking a highly skilled Medical Director / Senior Medical Director with a strong background in Gastroenterology to join our team. As a medical expert with specialized therapeutic expertise, you will be responsible for initiating and maintaining medical and consultative relationships with clients, consulting on early engagement and...


  • Alcobendas, Madrid, España Parexel A tiempo completo

    Job SummaryParexel is seeking a highly skilled Medical Director / Senior Medical Director with a strong background in Gastroenterology to join our team. As a medical expert with specialized therapeutic expertise, you will be responsible for initiating and maintaining medical and consultative relationships with clients, consulting on early engagement and...


  • Alcobendas, Madrid, España Parexel A tiempo completo

    At Parexel, we believe in the power of shared values to drive success. Parexel, a premier Clinical Research Organization (CRO), is in search of a distinguished Senior Regulatory Affairs Advisor (Associate Director level) with a strong background in Chemistry, Manufacturing, and Controls (CMC) for biological products and/or vaccines. The successful...


  • Alcobendas, Madrid, España Stryker Group A tiempo completo

    Job SummaryThe Senior Regulatory Affairs Specialist will be responsible for implementing and improving Stryker's regulatory and post-market surveillance system, quality management system, and environmental management system in Iberica. The focus will be on ensuring the safety of healthcare professionals and patients who come into contact with the company's...


  • Alcobendas, Madrid, España Stryker Group A tiempo completo

    Job SummaryThe Senior Regulatory Affairs Specialist will be responsible for implementing and improving Stryker's regulatory and post-market surveillance system, quality management system, and environmental management system in Iberica. The focus will be on ensuring the safety of healthcare professionals and patients who come into contact with the company's...


  • Alcobendas, Madrid, España Stryker A tiempo completo

    Job SummaryThe Senior Regulatory Affairs Specialist will be responsible for implementing and improving Stryker's regulatory and post-market surveillance system, quality management system, and environmental management system in Iberica. This role will ensure the safety of healthcare professionals and patients who come into contact with the company's medical...


  • Alcobendas, Madrid, España Stryker A tiempo completo

    Job SummaryThe Senior Regulatory Affairs Specialist will be responsible for implementing and improving Stryker's regulatory and post-market surveillance system, quality management system, and environmental management system in Iberica. This role will ensure the safety of healthcare professionals and patients who come into contact with the company's medical...


  • Alcobendas, Madrid, España Stryker Group A tiempo completo

    About the RoleThe Stryker Group is seeking a highly skilled Senior Regulatory Affairs Specialist to join our team in Madrid. As a key member of our Quality Management team, you will be responsible for implementing and improving our regulatory and post-market surveillance system, ensuring the safety of healthcare professionals and patients who come into...


  • Alcobendas, Madrid, España Stryker Group A tiempo completo

    About the RoleThe Stryker Group is seeking a highly skilled Senior Regulatory Affairs Specialist to join our team in Madrid. As a key member of our Quality Management team, you will be responsible for implementing and improving our regulatory and post-market surveillance system, ensuring the safety of healthcare professionals and patients who come into...


  • Alcobendas, Madrid, España Stryker A tiempo completo

    About the RoleThe Senior Regulatory Affairs Specialist will play a key role in ensuring the safety and quality of Stryker's medical device products. This position will be responsible for implementing and improving the company's regulatory and post-market surveillance system, as well as the Quality Management system and Environmental management system in the...


  • Alcobendas, Madrid, España Stryker A tiempo completo

    About the RoleThe Senior Regulatory Affairs Specialist will play a key role in ensuring the safety and quality of Stryker's medical device products. This position will be responsible for implementing and improving the company's regulatory and post-market surveillance system, as well as the Quality Management system and Environmental management system in the...


  • Alcobendas, Madrid, España Precision Medicine Group A tiempo completo

    About the RoleWe are seeking an experienced Project Manager or Senior Project Manager to join our global team at Precision Medicine Group. As a key member of our clinical trials team, you will be responsible for overseeing the delivery of full-service clinical projects across global and regional trials in Oncology, Rare Diseases, and CNS.Key...


  • Alcobendas, Madrid, España Precision Medicine Group A tiempo completo

    About the RoleWe are seeking an experienced Project Manager or Senior Project Manager to join our global team at Precision Medicine Group. As a key member of our clinical trials team, you will be responsible for overseeing the delivery of full-service clinical projects across global and regional trials in Oncology, Rare Diseases, and CNS.Key...

  • Senior RAQA Specialist

    hace 4 semanas


    Alcobendas, Madrid, España Stryker A tiempo completo

    Work Flexibility: HybridThe Job's MissionBased in Madrid, the Senior RAQA Specialist is responsible for implementing and improving Stryker's regulatory and post market surveillance system, the Quality Management system and the Environmental management system in Iberica.The focus is on ensuring the safety of health care professionals and patients that come...