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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 Medical Director provides medical and scientific oversight for clinical research programs, serving as the primary medical monitor for sponsor-dedicated studies. Responsibilities include protocol development, safety monitoring, SAE reporting, and providing medical expertise to project teams throughout the clinical trial lifecycle.
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.
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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.
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.
The Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining high-quality study documentation. They will also manage site relationships, support patient recruitment, and validate study data throughout the clinical trial lifecycle.
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.
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.
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 Medical Director oversees the execution of clinical trials in Neuroimmunology, specifically focusing on Lupus SLE, for a top-5 pharma client. Responsibilities include developing clinical development plans, overseeing medical writing for protocols, and managing clinical teams and scientific risks.
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.
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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The role involves serving as a statistical resource to mentor biostatisticians and oversee the preparation of Statistical Analysis Plans and clinical study reports. Additionally, the position focuses on maintaining R-based computing environments and developing Rshiny applications for data visualization.
Provide statistical support to the Medical Affairs group focusing on exploratory analysis, observational studies, and real-world evidence. Manage the statistical lifecycle of projects from protocol development to the final clinical study report.
Provide medical leadership and support for clinical trials, including the creation of protocols and real-time medical monitoring of study subjects. Serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and safety.
Conduct 45-minute online psychological counseling sessions to help clients improve their mental well-being. Identify client needs and provide individualized, sustainable solutions for issues ranging from stress to career growth.
The consultant supports operational staff in using ADaM and define.xml for statistical analysis within Medidata standards. They are responsible for developing efficiency tools, managing metadata repositories, and consulting with clients on CDISC implementation projects.
Oversee, train, and performance manage a team of clinical operations staff using metrics and KPIs. Ensure adherence to SOPs and WPDs while collaborating with leadership on resourcing and strategic planning.
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The specialist will plan, implement, and monitor the overall study supply chain strategy to maximize efficiency and minimize costs. This includes managing inventories of study drugs and collaborating with project management and vendors to optimize delivery processes.
Remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects and caregivers. Provide central monitoring by reviewing neuropsychological test batteries to ensure accuracy in administration and scoring.
Provide strategic medical and scientific expertise in hematology-oncology to support proposal development, protocol design, and clinical development plans. Act as a subject matter expert and consultant throughout the research and development lifecycle to guide project teams and sponsors.
The role involves providing medical monitoring and pharmacovigilance support for clinical research projects to ensure successful delivery. Additionally, the position requires building client relationships and providing medical expertise during the drug development and protocol design phases.
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