Job Summary:We are seeking a highly organized and motivated Senior Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include...
We are seeking a highly skilled and experienced Senior Clinical Research Coordinator to join our expanding research team in Pennsylvania. The ideal candidate will bring advanced expertise in clinical trial coordination, regulatory compliance, and patient management, as well as leadership in supporting junior staff and contributing to study planning and execution. Key Responsibilities. Lead and oversee the coordination of multiple clinical trials ...
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20 sites across the US and Canada, with plans for further expansion. . . Artemis Research is a leading principal investiga...
Clinical Research Coordinator. Location: Brooklyn, NY. About Brooklyn Clinical Research. Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. Clinical-trial enrollment should accurately represent the broader population. In meeting this objective, we help improve therapeutic efficacy and safety for all individuals. The Senior Clinical Research Coordinator (“SCRC”) monitors all data manageme...
Summary. The primary responsibility of the Senior Clinical Research Coordinator is to coordinate and oversee a clinical trial, including the day-to-day operations, training and supervising research staff, recruiting patients, communicating with study clinic staff, and monitoring patient safety. The Senior Clinical Research Coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by fe...
The Senior Clinical Research Coordinator will perform and manage tasks that are critical to clinical research studies. The Senior Clinical Research Coordinator must ensure compliance with federal regulations, study protocol guidelines, as well as monitor study participants, and take a proactive approach to identify issues on an ongoing basis throughout the clinical research study. . To consistently embody AMR Clinical’s Core Values. United We Ach...
Gastro Health, LLC is a leading medical group made up of physicians and advanced practitioners specializing in the treatment of gastrointestinal disorders, nutrition, and digestive health. Our research division provides patient access to Phase I-IV clinical research initiatives relational to Gastroenterology and Hepatology throughout the world. Our mission is to provide outstanding medical care and an exceptional healthcare experience. Gastro Hea...
Must be located/based in Tampa, Florida. Location. On site, Tampa, FL. JOB SUMMARY. The Senior Clinical Research Coordinator at. Axiom Brain Health. is responsible for the coordination, implementation, and management of clinical research studies in accordance with Good Clinical Practice (GCP), Institutional Review Board (IRB) approvals, and regulatory requirements. This role serves as a subject-matter resource for junior staff, supports protocol ...
The Senior Clinical Research Coordinator will perform and manage tasks that are critical to clinical research studies. The Senior Clinical Research Coordinator must ensure compliance with federal regulations, study protocol guidelines, as well as monitor study participants, and take a proactive approach to identify issues on an ongoing basis throughout the clinical research study. To Consistently Embody AMR Clinical’s Core Values. United We Achie...
This position is responsible for managing, coordinating and implementing all components of clinical research protocols, including pre and post research activities, internal and external to the clinical setting. Responsible for the implementation and conducting of multiple, complex research projects in the Clinical Research Center. Manages comprehensive patient protocol treatment schedules to maintain compliance to study protocol requirements. Dev...