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Perform ongoing clinical data review, including reconciliation of third-party data and serious adverse events. Conduct user acceptance testing and quality control of clinical databases while maintaining relevant documentation.
The Senior Clinical Data Associate performs data management activities for Phase I-III clinical trials, including data review and reconciliation. They are also responsible for conducting User Acceptance Testing (UAT) and Quality Control (QC) of clinical databases.
The Medical Director serves as the Global Lead Medical Monitor for clinical trials, providing therapeutic expertise and protocol-specific training to project teams. They also contribute medical input to clinical development programs and support business development activities through proposal generation and sponsor meetings.
Perform manual, independent reviews of clinical trial interviews to ensure scoring accuracy, interview quality, and protocol adherence. Maintain clear documentation of review findings and scoring justifications while overseeing site performance and rater remediation.
The Clinical Data Associate assists the Data Manager with data cleaning, trial documentation, and database verification. They are also responsible for user registration in EDC/CTMS systems and reconciling data from external sources.
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The Clinical Trial Coordinator provides administrative and technical support for clinical trials, including site activation, documentation maintenance, and vendor management. They ensure study activities are performed accurately, on time, and in compliance with regulatory standards and client requirements.
Manage the full lifecycle of clinical site payment administration, including protocol schedules, startup payments, and invoiceable items. Ensure accurate configuration of site contracts and budgets while troubleshooting payment failures to maintain operational excellence.
The Safety Physician provides medical and operational oversight for end-to-end pharmacovigilance activities, including ICSR medical assessment and coding standards. They also lead quality control initiatives, support benefit-risk strategies, and act as a primary point of contact for cross-functional medical review requirements.
The Senior Clinical Team Manager directs and coordinates the technical and operational aspects of clinical trials to ensure successful completion within budget and timelines. They manage clinical and start-up activities, lead project teams, and maintain compliance with ICH GCP and regulatory standards.
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.
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.
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 translator will perform translation and localization tasks within the life sciences, medical, and clinical trials domains. They are expected to contribute to AI and language technology projects while maintaining high quality standards.
The Clinical Team Manager oversees all clinical operational and quality aspects of respiratory studies in compliance with ICH-GCP. This includes developing monitoring strategies, managing project financials, and leading clinical teams to ensure deliverables are met within contractual timelines.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves tracking study progress against milestones, managing resource allocation for CRAs, and ensuring regulatory compliance and data integrity.
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Provide high-quality medical information services via phone and email, answering technical product questions and handling adverse event reports. Translate medical documents between English and Spanish and ensure all inquiries are logged accurately in compliance with SOPs.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters on scoring techniques. Responsibilities include conducting live feedback sessions, performing mock interviews, and submitting accurate documentation.
Monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Coordinate study set-up activities and provide mentorship to junior staff while interacting directly with clients.
Monitor and manage clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Coordinate study set-up activities, mentor junior staff, and interact with clients regarding proposals and payments.
Provide high-quality mental health support through psychotherapy, counseling, or coaching sessions to clients in the Asia-Pacific and Europe regions. Responsibilities also include leading support groups and delivering educational Masterclasses.
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.
Remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects in pharmaceutical trials. Provide central monitoring by reviewing test batteries and recordings to ensure data accuracy and providing feedback to raters.
The role involves managing administrative tasks, triaging tickets and emails in Jira, and responding to payment queries from sites and sponsors. Additionally, the associate supports system migrations and study reconciliation activities through data preparation and tracking.
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.
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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.
Design and implement statistical strategies and analysis plans for clinical trials across various therapeutic areas. Perform SAS programming to generate study reports and provide expert guidance on methodology and sample size calculations.
Provide medical leadership and support for clinical trials in nephrology, including protocol creation and real-time medical monitoring. Act as the primary medical liaison between the sponsor and internal departments to ensure subject safety and study compliance.
The Director will engage with senior management to establish strategic department initiatives and drive business development activities for Clinical Assessment Technologies. They are also responsible for overseeing the development of assessment training content and ensuring all materials meet protocol and regulatory requirements.
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