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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 Senior Clinical Research Associate will oversee site monitoring, study management, and ensure the integrity of clinical trials. They will also act as a mentor to peers, assist in hiring and training, and serve as an escalation point for site or patient issues.
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.
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Provide best-in-class, evidence-based, and culturally affirming nutrition care to patients. Manage patient sessions, perform charting, and collaborate with a team of dedicated dietitians.
The Clinical Research Associate conducts qualification, initiation, monitoring, and closeout visits for research sites to ensure protocol compliance. They are responsible for verifying investigator qualifications, reviewing regulatory documents, and ensuring accurate data reporting in accordance with GCP and SOPs.
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 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.
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.
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.
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.
Provide high-quality mental health support through psychotherapy, counseling, or coaching sessions. Lead support groups and deliver masterclasses to clients across the Asia-Pacific region and Europe.
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