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Avalo Therapeutics
Overview
The Clinical Trial Associate will support the planning, execution, and delivery of clinical trials in compliance with regulatory standards and internal SOPs. Responsibilities include tracking study progress, managing vendor relationships, and ensuring the quality and completeness of trial documentation.
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Compensation
Salary not listed
Posted
7 days ago
Headlands Research
Support clinical trial delivery by preparing study documents, conducting patient procedures like vital signs and phlebotomy, and managing study data. Coordinate participant visits and ensure compliance with FDA and Good Clinical Practice guidelines.
10 days ago
The role involves supporting clinical trial visits by performing phlebotomy, collecting patient vitals, and managing biological samples. Additionally, the assistant handles study documentation, data entry into EDC/CTMS systems, and general administrative support for research coordinators.
Support clinical trials by preparing study documents, recruiting participants, and conducting patient-facing procedures like vital signs and phlebotomy. Manage study data entry in EDC and CTMS systems while ensuring compliance with FDA and GCP guidelines.
$22 - $27 / HOUR
Seattle Children's
The coordinator is responsible for recruiting and screening eligible participants and conducting study visits according to established protocols. They also manage data collection, ensure regulatory compliance, and maintain professional interactions with patients and families.
$29 - $44 / HOUR
29 days ago
The role involves recruiting and screening eligible participants for pulmonary research studies and coordinating study visits. It also requires managing data collection, ensuring regulatory compliance, and maintaining professional interactions with patients and families.
$88,786 - $133,180 / YEAR
Syneos Health
Coordinate and manage clinical research projects, including site preparation, patient recruitment, and data collection. Ensure all study activities comply with Good Clinical Practices (GCP) and regulatory requirements while supporting the Principal Investigator.
$49 - $59 / HOUR
1 month ago
Nationwide Children's Hospital
Assists with administrative components to ensure regulatory compliance for clinical research projects, including maintaining study binders and files. Prepares and submits IRB documents while ensuring accuracy across regulatory and grant systems.
Hoag
The Clinical Research Coordinator RN manages all aspects of FDA-regulated clinical trials, from protocol review and subject recruitment to data collection and regulatory maintenance. They work closely with study physicians to ensure the accurate execution of Phase I-IV trials and maintain compliance with Good Clinical Practices.
$49 - $76 / HOUR
Coordinate and manage clinical research projects, including site start-up, patient recruitment, and data collection. Ensure all study activities comply with Good Clinical Practices (GCP) and regulatory requirements while supporting the Principal Investigator.
Assists with administrative components to ensure regulatory compliance for clinical research projects. Responsibilities include maintaining study binders, submitting IRB documents, and collecting investigator credentials.
Johnson & Johnson Innovative Medicine
The Clinical Trials Assistant supports the clinical study team with project communications, site payments, and file management. They are responsible for maintaining clinical databases, processing regulatory documents, and ensuring study supplies are managed effectively.
$41,000 - $66,700 / YEAR
Pinnacle Clinical Research
The Clinical Research Coordinator manages daily clinical trial operations, including participant recruitment, screening, and study protocol adherence. They also ensure accurate documentation, regulatory compliance, and effective communication with sponsors and the research team.
Alliance for Clinical Trial in Oncology Foundation
The Clinical Research Associate will manage clinical trial operations, including site selection, study start-up, and maintenance of trial master files. They will collaborate with CROs and investigative sites to ensure compliance with ICH GCP guidelines and organizational standards.
2 months ago
CenExel
The coordinator ensures the highest standards of data quality and participant safety are maintained, along with adherence to protocols, SOPs, and regulatory guidelines. This involves assisting the QA Manager, reviewing various study documents for trends, and performing ongoing quality reviews of study records and documentation.
The Clinical Research Coordinator III is responsible for managing all aspects of complex clinical research trials, including drug, device, and biologic studies, while collaborating with physicians and stakeholders. Key duties involve conducting protocol review, administering informed consent, recruiting subjects, ensuring accurate data collection, completing CRFs, and overseeing adverse event reporting and subject follow-up.
$39 - $59 / HOUR
Professional Case Management
The Clinical Research Coordinator provides technical and administrative support to the clinical operations team while delivering direct patient care for research study participants, including assessing and following participants according to trial protocols. This role is accountable for regulatory compliance, performance of mobile clinics, patient engagement, screening, and ensuring timely and accurate Electronic Data Capture (EDC) data entry and query resolution.
$54,080 - $74,880 / YEAR
The Clinical Research Coordinator will provide technical and administrative support to the clinical operations team while delivering direct patient care for research study participants, including assessing and following participants per trial protocols. This role is accountable for regulatory compliance, performance of mobile clinics, patient engagement, screening, and ensuring timely and accurate Electronic Data Capture (EDC) data entry and query resolution.
The Patient Care Technician assesses participants' psychosocial and case management needs, observes behavior changes, and assists subjects with ADLs, meals, laundry, and housekeeping while ensuring strict adherence to study protocols. Responsibilities also include coordinating discharge planning, managing necessary documentation, and developing relationships with external agencies to support participant services.
$20 - $21 / HOUR
3 months ago
The coordinator ensures the highest standards of data quality and participant safety are maintained, along with adherence to protocols, SOPs, and regulatory guidelines. This involves assisting the QA Manager, reviewing various monitoring reports and logs for trends, and performing ongoing quality reviews of study documentation.
