Jobs 1 - 20 out of 22 for Clinical Trial Coordinator

Trial coordination of allocated clinical trials within the framework of Good Clinical Practice. Responsible for the delivery of clinical-trial-related care of patients, completing study related procedures and associated documentation, coordinating patient visits and scheduling, maintaining communica...

Company Description Here at the Sunshine Coast University Private Hospital (SCUPH), we are proud to offer advanced facilities, including 9 state-of-the-art operating theatres, two cardiac catheter laboratories, a minor procedure room, a day surgery unit, an 11 bed intensive care unit/coronary care ...

Provides Trial Management Filing (TMF) system support, including document inspection, filing, and auditing. Supports study budget negotiation and contract finalization related to study providers and investigator sites. Manages study and site materials, reviews informed consents, and ensures complian...

Job Title: Clinical Trial SpecialistJob Description The Clinical Trial Specialist coordinates and supports all aspects of clinical research studies from initiation through activation and ongoing conduct. This role focuses on oncology clinical trials and involves preparing study tools, managing regu...

The Clinical Trial Coordinator is responsible for implementing and supporting multiple clinical trial programs across SiteLabs' decentralized pharmacy network. You will act as the primary liaison between pharmacies, clinical partners, and SiteLabs internal teams. Responsibilities include onboarding ...

The Clinical Trial Coordinator is responsible for implementing and supporting multiple clinical trial programs across SiteLabs' decentralized pharmacy network. You will act as the primary liaison between pharmacies, clinical partners, and SiteLabs internal teams, ensuring sites are equipped, complia...

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians and institutions to develop elegant medical devices. Our products are being u...

Assist with the development of protocol, policies, and procedures, documentation and training of new staff, participate in protocol development and audits, ensure compliance with FDA and IRB requirements, provide agendas for meetings, contribute to scientific writing, monitor study progress, maintai...

Overview Black Canyon Consulting (BCC) is searching for a Clinical Trials Coordinator to support our work for the National Center for Complementary and Integrative Health (NCCIH). This opportunity is part-time, 20-30 hours per week, and onsite at the NIH-NCBI in Bethesda, MD and/or remote work. Duti...

The Division of Clinical Research provides infrastructure support for all aspects of clinical research. UT MD Anderson has the nation's largest cancer clinical trials program enrolling patients in Texas and beyond through our Cancer Network® partners across the country. UT MD Anderson is devoted to ...

PRiSMS Group facilitates Clinical Trial programs for community hospital systems. We specialize in cancer and cardiovascular therapeutics. Position: Clinical Research Coordinator (CRC) comprises an integral part of the research team. Working under the Lead Physician, he/she is responsible for conduct...

The Clinical Trial Laboratory Coordinator ensures high-quality protocol execution, compliance, and efficiency in clinical research laboratory operations. Responsibilities include protocol development, quality assurance, specimen collection oversight, and clinical trial inventory management. The coor...

At Houston Methodist, the Research Coordinator position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. This position ensures accurate data collection, documentation, organization and...

Coordinate the day-to-day activities of research protocols, assess and determine qualification of patients for research studies, ensure accurate data collection and documentation, and maintain safety of research participants. Conduct screening and interviews to evaluate patient eligibility, schedule...

The Regulatory Coordinator II (RC II) will work under the direction of the Director of Clinical Research Administration for the Clinical Trials Office to complete the regulatory requirements of the clinical research projects. The RC coordinates aspects of protocol submissions, prepares and submits r...

Provides Trial Management Filing (TMF) system support, including document inspection, filing, and auditing. Supports study budget negotiation and contract finalization related to study providers and investigator sites. Manages study and site materials and reviews informed consents. Provides feedback...

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians and institutions to develop elegant medical devices. Our products are b...

At Houston Methodist, the Research Coordinator position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. This position ensures accurate data collection, documentation, organization and...

Support the Clinical Operations Team by assisting with the management and inventory of clinical supplies, ensuring materials are available at clinical sites, and supporting multiple Clinical Trials. Conduct reviews of trial data and follow GCP/ICH protocols/guidelines, including travel to Clinical s...

Support the planning, coordination, and execution of clinical trials in accordance with applicable protocols and regulations. Maintain accurate trial documentation, manage trial master files, and track study milestones. Liaise with clinical sites, CRO partners, and internal cross-functional teams to...