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Manage day-to-day clinical trial operations, ensuring adherence to timelines, budget, and quality standards. Collaborate with cross-functional teams to implement protocols while building strong relationships with investigators and stakeholders.
The Clinical Independent Rater reviews assessment quality and provides guidance to raters on methodology and scoring techniques. They also conduct patient interviews and administer clinical rating scales while ensuring protocol compliance and data integrity.
You will lead and develop a team of clinical consulting professionals to deliver Radiology Informatics implementation services across Central and Eastern Europe. The role involves partnering with sales and implementation teams to validate solution designs and ensure successful clinical adoption of Philips solutions.
The Clinical Development Liaison will serve as a scientific bridge between investigators and internal stakeholders to support clinical trial start-up, patient recruitment, and study execution. They will establish trusted relationships with healthcare professionals and provide scientific expertise to ensure high-quality study conduct across the Benelux region.
The manager is responsible for shaping and executing enterprise account strategies to build long-term, transformational partnerships with strategic healthcare customers. They will lead the full opportunity lifecycle, manage total account revenue, and drive cross-functional collaboration to deliver integrated medical solutions.
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The Principal Biostatistician leads statistical activities across multiple studies, serving as the primary sponsor contact and providing expert consultancy on study design and protocol development. They also oversee project deliverables, mentor junior staff, and ensure compliance with regulatory standards throughout the clinical trial lifecycle.
You will coordinate all aspects of the clinical monitoring and site management process to ensure trial compliance with protocols and regulatory standards. This includes conducting remote or on-site visits, managing documentation, and ensuring data reliability through rigorous review and problem-solving.
The role involves coordinating all aspects of clinical monitoring and site management to ensure trials are conducted according to protocols and ICH-GCP guidelines. You will perform risk-based monitoring, ensure data accuracy, and maintain collaborative relationships with investigational sites.
The nurse will conduct patient home visits to support clinical trial sites by performing IV infusions, collecting vital signs, and processing blood draws. This role is performed on an ad hoc basis and can be managed alongside other professional commitments.
The Senior Manager will lead global Medical Affairs strategies, fostering partnerships with Key Opinion Leaders and managing scientific evidence generation. They will also provide medical leadership throughout the product lifecycle and ensure all communications comply with regulatory and ethical standards.
The Senior Clinical Research Associate is responsible for site management and monitoring activities across the country for a single sponsor. They will drive subject recruitment plans, provide protocol training, and maintain monitoring visit reports.
The Principal Biostatistician serves as the statistical lead for late-phase clinical trials, providing scientific oversight and strategic guidance. They are responsible for authoring statistical analysis plans, performing complex analyses, and representing the biostatistics function within cross-functional clinical teams.
The Associate Tutor is responsible for delivering high-quality instructor-led training courses on standards such as ISO 13485 and ISO 7101. They must facilitate engaging learning experiences while ensuring compliance with BSI methodologies and accreditation requirements.
The specialist manages clinical trial site activities, including site activation, protocol training, and case coverage to ensure efficient study conduct. They also maintain strong relationships with investigators and provide continuous status updates to internal clinical trial leaders.
The Medical Director provides medical leadership for clinical trials, including protocol development, medical monitoring, and safety evaluation. They serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and effective issue resolution.
The Senior Clinical Pharmacologist will lead clinical pharmacology strategies across early and late-phase drug development programs while partnering with cross-functional teams to drive decision-making. They will apply model-informed drug development principles to support dose selection, biomarker optimization, and regulatory submissions.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to pediatric subjects in clinical trials. They are also responsible for scoring assessments and providing central monitoring to ensure data accuracy and quality.
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The Local Clinical Trial Manager is responsible for leading local study teams and ensuring clinical deliverables meet time, budget, and quality expectations. They serve as the operational point-of-contact, managing site selection, regulatory submissions, and vendor oversight to ensure study integrity.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects via tele-health platforms. They are also responsible for scoring assessments and providing central monitoring of neuropsychological test data to ensure accuracy.
The role involves conducting patient interviews and clinical assessments while ensuring the integrity and reliability of clinical trial data. The rater will provide guidance to other raters on methodology and scoring techniques through live interactions.
The incumbent will lead medical science and strategy for metabolic clinical research, providing expert input on development plans, regulatory issues, and clinical trial protocols. They will also engage in business development, support client proposals, and mentor internal clinical teams to ensure high-quality delivery of research projects.
The incumbent will lead medical science and strategy for oncology, driving business outcomes through proposal development, client engagement, and strategic clinical trial design. They will also provide therapeutic expertise to internal teams, mentor clinical scientists, and contribute to innovative clinical research initiatives.
The Clinical Research Monitor ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and company procedures. They also manage relationships with investigators and site staff to support study initiation, patient recruitment, and data reporting.
The Clinical Specialist is responsible for reviewing clinical trial data and assessment scales to ensure standardized practices and data integrity. They provide guidance to raters through live discussions, feedback, and functional assessments like mock interviews.
Perform manual, independent reviews of clinical trial interviews and scale administrations to ensure scoring accuracy and protocol adherence. Senior roles involve clinical decision-making regarding site performance and overseeing rater remediation.
Serve as the primary medical and scientific strategic lead for psychiatry-focused clinical studies and business development. Collaborate with cross-functional teams to design protocols, execute study strategies, and provide expert medical input for internal and external stakeholders.
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The Field Trainer will lead in-person clinical training sessions to help dental practices adopt intraoral scanning and digital workflows. They will also act as a clinical advisor, monitoring practice outcomes and providing coaching to ensure long-term success.
Manage a portfolio of Medical Device CE marking schemes and conduct technical reviews within the IVD sector. Provide leadership in Quality Management Systems and offer technical support to the commercial team.
The Director will drive regional IoT/OT revenue by executing targeted strategies and managing a healthy pipeline in the European region. They will also partner with Sales and Channel teams to close complex enterprise deals while providing technical leadership to shape future product roadmaps.
The EHS Manager is responsible for the global oversight, standardization, and alignment of the organization’s EHS framework across international aviation operations. This role develops global policies, monitors regional conformance, and supports independent assurance activities to ensure safety and regulatory compliance.
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