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The Adult Research Nurse will manage daily trial operations, including protocol adherence, data documentation, and patient assessments. They will also coordinate trial visits, administer medication, and ensure accurate reporting of adverse events while maintaining effective communication with the research team.
The Principal Biostatistician leads biomarker-related statistical activities across clinical studies, serving as the primary contact for sponsors. They are responsible for developing biomarker evaluation plans, conducting advanced data analysis, and mentoring junior staff to ensure high-quality deliverables.
The Principal Biostatistician leads statistical activities across multiple studies, serving as the primary sponsor contact and providing expert consultancy on study design and protocol development. They also oversee project deliverables, mentor junior staff, and ensure compliance with regulatory standards throughout the clinical trial lifecycle.
You will source, screen, and engage qualified healthcare professionals while managing the full recruitment cycle from search to placement. Additionally, you will build a strong candidate pipeline and collaborate with clients to meet hiring targets.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They act as a cross-functional liaison, manage study documentation, and facilitate communication between internal teams and clinical sites.
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The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They also manage study documentation, perform file reviews, and act as a liaison for cross-functional project initiatives.
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.
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.
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 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 manager provides leadership for the operational and financial aspects of clinical trial supplies throughout the project life cycle. They are responsible for vendor management, inventory planning, and ensuring compliance with regulatory standards and study requirements.
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 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.
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.
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 Principal Biostatistician serves as a resource for the statistical department, mentoring biostatisticians and overseeing training plans. They provide support across all statistical tasks during the project lifecycle and ensure high-quality work is completed on time.
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Advocates assess and evaluate refugee clients for vulnerability in preparation for asylum interviews and provide crisis intervention assistance. They also offer general mental health and trauma support to the Advocates Abroad teams.
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