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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.
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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.
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.
Develop and update promotional medical content for various digital and print commercial assets while ensuring compliance with Dutch regulatory guidelines. Collaborate with design, brand, and production teams to translate complex scientific data into clear, engaging, and accurate communication materials.
The Senior Clinical Research Associate conducts site monitoring visits in the Netherlands and Belgium to ensure protocol compliance and data integrity. They provide leadership and guidance to the clinical team while managing study budgets and site-related issues.
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.
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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.
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.
Lead day-to-day clinical trial operations from start-up through close-out while managing study timelines and enrolment targets. Provide oversight of CRA activities, ensure protocol compliance, and manage relationships with sponsors and investigators.
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 Senior Manager will foster and maintain strategic relationships with electrophysiologists and key accounts across the EMEA region. They will act as a liaison between the organization and stakeholders to ensure consistent service, strategic engagement, and effective collaboration.
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.
The Medical Director provides medical leadership and strategic direction for clinical development programs, ensuring study protocols meet scientific and regulatory standards. They serve as a Medical Monitor, interpret clinical trial data, and collaborate with multidisciplinary teams to drive successful program execution.
You will provide critical diagnostic information for veterinary patients while receiving mentorship and feedback from experienced radiologists. The role involves reading both known and live cases to prepare for board certification and maintain high reporting standards.
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Manage the performance and workload of medical writers while overseeing the preparation and quality of publication deliverables. Lead resource planning, budget preparation, and the development of departmental training programs and SOPs.
Manage the end-to-end medical licensing and onboarding process for physicians and nurses in a multi-state telehealth environment. Ensure compliance with state and federal regulations while acting as the primary liaison with medical boards.
Monitor and manage the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Coordinate all necessary activities for study setup, including identifying investigators and preparing regulatory submissions.
The CRA II will monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Responsibilities include coordinating study setup activities, identifying investigators, and managing regulatory submissions.
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