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Clinical Research Coordinator II
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17 roles found

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HealthcareFull-time
Houston, TXScience & PharmaceuticalPosted 17d ago

Responsibilities Develop strong working relationships and become the point of contact for the clinic as well as the sponsor for clinic related activities Manage multiple concurrent trials Assist with mentoring and training study team members Maintain required records of study activity including study logs, case report forms, and/or regulatory forms Schedule volunteers for appointments, procedures and inpatient stays

HealthcareFull-time
Seattle, WAScience & PharmaceuticalPosted 17d ago

Responsibilities Assist the assigned division research team within the organization, implementation and completion of clinical research trials Maintain regulatory documents; assist the Principal Investigator in the planning of protocol implementation and site initiation visits and routine monitoring of clinical studies Along with the PI, ensure that research projects are conducted in compliance with federal regulatio

HealthcareFull-time
Peoria, ILScience & PharmaceuticalPosted 17d ago

Alpha Home Health and Hospice seeks a Clinical Research Coordinator II to coordinate clinical investigations and ensure compliance with federal regulations, GCP, and institutional policies. The role maintains accurate study data and documentation, verifies protocol adherence, and supports study participants, research teams, sponsors, and the IRB. Responsibilities Coordinates research studies, designs source documents

HealthcareFull-time
Celebration, FLScience & PharmaceuticalPosted 18d ago

AdventHealth hires a Clinical Research Coordinator II to coordinate and oversee multiple clinical trial protocols, ensuring accurate documentation, patient advocacy, regulatory compliance, and trial integrity. The role collaborates with investigators, support staff, sponsors, and institutional partners throughout study start-up, execution, and closeout. Responsibilities Manages multiple clinical trial protocols, coor

HealthcareFull-time
Memphis, TNScience & PharmaceuticalPosted 19d ago

Responsibilities Prioritize activities with specific regard to protocol timelines Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials Maintain effective relationships with study participants and other care Access Research personnel Balances protocol needs with patient experience; proactively addresses concerns Monitors quality metrics; prevents deviations; resolves qu

HealthcareFull-time
Lubbock, TXScience & PharmaceuticalPosted 19d ago

Iterative Health is hiring a Clinical Research Coordinator II to independently coordinate clinical trials from start-up through closeout, ensuring protocol compliance, regulatory standards, and patient safety. The role manages study activities, patient recruitment and retention, documentation and data quality, and communication with participants, investigators, sponsors, and CROs. Responsibilities Independently coord

HealthcareFull-time
Worcester, MAScience & PharmaceuticalPosted 19d ago

Responsibilities Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data Conduct preliminary quality assurance reviews of s

HealthcareFull-time
Dallas, TXScience & PharmaceuticalPosted 19d ago

Adams Clinical is a clinical trial site network specializing in late-phase industry-sponsored trials for psychiatric and neurological conditions. The Clinical Research Coordinator II independently manages complex or high-enrolling clinical trials, oversees study operations and participant visits, supports study start-up, and maintains data quality and inspection readiness. The role also serves as a liaison with spons

HealthcareFull-time
Rockville, MDScience & PharmaceuticalPosted 20d ago

Responsibilities Collaborating with principal investigators and other research staff to develop, implement, and monitor clinical research protocols. Timely reporting of adverse events to investigators and research team leadership Coordinating all aspects of clinical research studies, including participant recruitment, screening, enrollment, and follow-up visits Performing clinical procedures, including taking vitals,

HealthcareFull-time
Nashville, Tennessee, USAScience & PharmaceuticalPosted 21d ago

Meharry Medical College is a higher education institution focused on health sciences. They are seeking a Clinical Research Coordinator II to independently coordinate advanced clinical research projects, ensuring compliance with regulatory guidelines and institutional policies. The role involves managing study activities, maintaining records, assisting with financial functions, and supporting the Principal Investigato

HealthcareFull-time
Los Angeles, CAScience & PharmaceuticalPosted 22d ago

Children's Hospital Los Angeles (CHLA) is hiring a Clinical Research Coordinator II to administer clinical trials across all protocol phases. The role supports study teams and principal investigators with recruitment, data collection, study scheduling and follow-up, data quality assurance and control, and cross-coverage for other coordinators. Responsibilities The Clinical Research Coordinator II, as a certified rese

HealthcareFull-time
Salt Lake City, UtahScience & PharmaceuticalPosted 25d ago

Job Description: Advance Life-Changing Clinical Research Join Intermountain Health as a Clinical Research Coordinator and play a key role in advancing innovative clinical studies that improve patient outcomes. In this patient-facing position, you will partner with physicians, investigators, research participants, and sponsors to coordinate complex research protocols while ensuring regulatory compliance and exceptiona

Clinical Research Coordinator II

$42,500.00- $59,500.00

HealthcareFull-time
Boston, MassachusettsScience & PharmaceuticalPosted 27d ago

The Clinical Research Coordinator II will play a key role in supporting research activities within the Translational Research Laboratory and Biospecimen Repository in the Section of Hematology & Medical Oncology. Primary responsibilities include obtaining informed consent for research studies and biobank enrollment, abstracting data from medical records, maintaining patient databases, and processing and managing bios

Clinical Research Coordinator II

$42,500.00- $59,500.00

HealthcareFull-time
Boston, MassachusettsScience & PharmaceuticalPosted 27d ago

The Clinical Research Coordinator II will play a key role in supporting research activities within the Translational Research Laboratory and Biospecimen Repository in the Section of Hematology & Medical Oncology. Primary responsibilities include obtaining informed consent for research studies and biobank enrollment, abstracting data from medical records, maintaining patient databases, and processing and managing bios

HealthcareFull-time
Rochester, NYScience & PharmaceuticalPosted 30+ Days Ago

Bausch + Lomb is a global eye health company dedicated to protecting and enhancing sight through its portfolio of eye health products. The Clinical Research Coordinator II independently coordinates and oversees clinical studies of moderate complexity, ensuring study objectives, timelines, documentation, and regulatory requirements are met. The role also leads study start-up and close-out activities, resolves operatio

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