Medical Device Clinical Safety Scientist

For our client, an international pharmaceutical company, we are currently looking for a Medical Device Clinical Safety Scientist.

Location: Basel

Contract: 6 months (extension likely)

Tasks & Responsibilities:

• Provide expert leadership and oversight for all clinical safety and vigilance activities associated with Class II and/or III Medical Devices (MD), ensuring adherence to global regulatory requirements and internal standards throughout the product lifecycle.
• Oversee and execute the MD vigilance process, including the intake, assessment, processing, and reporting of adverse events, ensuring timely and compliant submissions to regulatory bodies.
• Review core Medical Device study documentation to ensure comprehensive and accurate inclusion of safety-related content, including documents such as the Clinical Investigation Plan (CIP/Protocol) and Investigator's Brochure (IB).
• Develop, maintain, and ensure the accuracy and timely updates of Reference Safety Information (RSI) for clinical investigations, incorporating emerging safety data and ensuring proper dissemination.
• Lead or significantly contribute to benefit-risk assessments for Medical Devices, providing expert analysis of clinical safety data to guide regulatory and strategic business decisions.
• Ensure the integration of MD risk management principles within clinical safety processes, aligning activities with ISOstandards for risk management in medical devices.
• Act as the subject matter expert for all safety-related activities in MD clinical investigations.
• Maintain an advanced understanding of ISO:2020 principles and apply them effectively to the design, execution, monitoring, documentation, and reporting of clinical investigations, with a strong focus on safety reporting and subject protection.

Must-Haves:

• Bachelor's, Master's, or PhD in a scientific field.
• At least 3 years of relevant experience in healthcare, scientific research, or biomedical research focused on clinical safety, with hands-on experience in the use of MDs and/or combination products within the pharmaceutical, biotech, or medical device industries.
• Strong understanding of the technical and biomedical aspects of Medical Devices.
• Solid working knowledge of applicable regulations and industry standards for Medical Devices.
• Significant expertise in MD clinical investigations, with hands-on experience in safety activities related to Class II and/or III MD clinical investigations. Demonstrated ability to take on roles with safety responsibilities in MD clinical studies.
• Advanced understanding of ISO:2020 and the ability to apply this standard effectively across all phases of MD clinical investigations. Proven capability to integrate ISOprinciples into practice.
• Experience in developing and providing safety input for core MD clinical investigation documents, including the Clinical Investigation Plan (CIP/Protocol), Investigator's Brochure (IB), and Reference Safety Information (RSI). Demonstrated ability to strategically lead the development of these deliverables independently.
• Demonstrable experience in MD benefit-risk assessments and practical application of risk management principles as per ISOstandards.
• Familiarity with combination products (drug/MD).
• Direct experience in clinical safety and vigilance activities for Medical Devices.