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The role provides scientific support for epidemiology studies by conducting literature reviews, data cleaning, and quality control activities. It also involves coordinating operational tasks across multiple studies to ensure high-quality execution and cross-functional alignment.
The Medical Science Liaison will serve as a field-based scientific expert, engaging with healthcare professionals and key opinion leaders to provide balanced medical information. They will also support clinical trial progress and gather competitive intelligence to inform strategic decision-making within the hemato-oncology therapeutic area.
The Clinical Project Leader is responsible for leading cross-functional teams to deliver clinical trials on time, within budget, and in compliance with ICH GCP standards. They manage client relationships, project P&L, risk mitigation, and ensure high-quality project deliverables.
The Centralized Monitoring Analyst is responsible for setting up and programming the Centralized Monitoring platform, including QTLs, KRIs, and data visualizations. They also support the Centralized Monitoring Lead in developing study-specific strategies and maintaining platform specifications.
The Clinical Project Leader is responsible for leading cross-functional teams to deliver clinical trials on time, within budget, and in compliance with ICH GCP standards. They manage client relationships, project plans, risk mitigation, and financial performance including revenue recognition and forecasting.
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The Senior Manager, Clinical Operations acts as the Clinical Process Owner, responsible for the governance, harmonization, and lifecycle management of clinical operations SOPs and documentation. They lead cross-functional initiatives to ensure processes are compliant, scalable, and effectively implemented across the organization.
The Senior Manager, Clinical Operations serves as the Clinical Process Owner, responsible for the governance, harmonization, and lifecycle management of clinical operations processes. They lead cross-functional initiatives to ensure processes are compliant, scalable, and effectively implemented across the organization.
The Senior Clinical Trial Manager provides leadership and direction to clinical site management teams while overseeing regional CTMs and coordinating study activities. They are responsible for developing monitoring strategies, managing budgets, and ensuring compliance with clinical protocols and regulatory requirements.
The Clinical Payments Specialist manages end-to-end global investigator payments, including setup, deployment, and reconciliation of study payment solutions. They act as a liaison between investigative sites and clinical teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
The Clinical Payments Specialist manages end-to-end investigator payments, including setup, deployment, and reconciliation for assigned studies. They act as a liaison between investigative sites and internal teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
The Senior Decentralized Clinical Trial Study Lead is responsible for the strategic development and delivery of decentralized clinical trials, ensuring they meet quality, speed, and financial objectives. They act as the primary point of contact for customers and lead cross-functional teams to manage study milestones, risks, and project performance.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects. They are also responsible for scoring assessments and providing central monitoring of neuropsychological test data to ensure accuracy.
You will oversee clinical trial management workstreams, ensuring all deliverables meet quality, timeline, and regulatory standards. This includes collaborating with cross-functional teams to implement protocols, manage budgets, and optimize study outcomes through data analysis.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, conduct site visits, and manage documentation to maintain audit readiness.
The Medical Director will provide expert medical monitoring and leadership for clinical research projects, ensuring compliance with protocols and safety standards. They will also support business development, mentor junior staff, and maintain strong consultative relationships with clients.
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.
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The role involves leading clinical trial start-up activities, including site activation and the preparation of essential regulatory documents. You will collaborate with cross-functional teams to streamline processes and provide guidance to study teams to ensure compliance and project success.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are performed accurately. Responsibilities include managing system access, maintaining project documentation, and performing quality audits on trial files.
The Clinical Rater performs manual, independent reviews of clinical trial interviews and scale administrations to ensure scoring accuracy and protocol adherence. They maintain detailed documentation of findings and, in senior roles, oversee site performance and rater remediation.
Lead statistical strategy and delivery for complex clinical trials, ensuring high-quality outputs and regulatory compliance. Provide technical leadership, mentor junior staff, and collaborate with multidisciplinary stakeholders to support global programs.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites to ensure subject safety and data integrity. They collaborate with study teams and sponsors to maintain protocol compliance and manage investigational product accountability.
The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also provide guidance to raters through live interactions, feedback, and functional assessments.
Deliver clinical education and training for the Women’s Health ultrasound portfolio to customers and internal teams. Collaborate with management to identify market trends and execute strategies for expanding into new care areas.
The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality. They also review assessments conducted by other raters to maintain protocol compliance and provide feedback on scoring techniques.
Deliver high-quality clinical and technical ultrasound training to customers while identifying emerging market trends and unmet clinical needs. Collaborate with product managers to execute commercial strategies and support the adoption of new technologies within the Women's Health segment.
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The Clinical Project Leader will provide cross-functional leadership for clinical trials, ensuring projects are delivered on time, within budget, and in compliance with ICH GCP standards. They are responsible for managing client relationships, project P&L, and mitigating risks throughout the project lifecycle.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing clinical project teams, tracking study progress against milestones, and ensuring regulatory compliance and data integrity.
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