Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
St. Elizabeth Healthcare
Overview
Coordinate clinical research studies by managing subject enrollment, data collection, and regulatory compliance. Collaborate with physicians to open new studies and ensure adherence to protocol and FDA guidelines.
Quick view →
Compensation
Salary not listed
Posted
16 days ago
Tufts Medicine
This role involves assisting the Principal Investigator in planning and implementing clinical research studies, including participant recruitment, screening, and follow-up activities. Responsibilities also cover maintaining regulatory compliance, managing study documentation, performing basic lab activities, and coordinating data collection and query resolution.
$47,924 - $59,895 / YEAR
29 days ago
CenExel
Responsible for conducting basic to moderately complex diagnostic testing and managing laboratory samples according to study protocols. Duties include maintaining harvest logs, monitoring storage temperatures, and ensuring adherence to FDA and GCP guidelines.
$20 - $25 / HOUR
1 month ago
Performs diagnostic testing and basic laboratory activities across disciplines such as hematology and chemistry. Responsible for sample collection, storage, documentation, and adherence to FDA and GCP guidelines.
$19 - $23 / HOUR
Performs diagnostic testing and basic laboratory activities across disciplines such as hematology and chemistry. Responsible for sample collection, storage, and strict adherence to FDA and GCP guidelines.
$19 - $24 / HOUR
The laboratory technician performs diagnostic testing and manages laboratory activities including sample collection, processing, and storage. They ensure adherence to clinical protocols, FDA regulations, and GCP standards while maintaining accurate laboratory logs and inventory.
TIDEWATER PHYSICIANS MULTISPECIALTY GROUP P C
The Clinical Research Coordinator manages the daily operations of clinical studies, including patient enrollment, protocol compliance, and data collection. They also handle laboratory specimens, maintain regulatory documentation, and coordinate with investigators and sponsors to ensure study success.
2 months ago
UCSF
The Clinical Research Coordinator will assist with implementing study protocols, coordinating clinical trials, and managing data and specimen collection. They will also recruit and screen study participants while interacting with healthcare providers and research staff.
Hoag
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
HonorHealth
The Coordinator II acts as the primary contact for the study sponsor, managing day-to-day project activities, resources, and overall clinical data and protocol management for clinical trials at HonorHealth. Essential functions include managing complex protocols involving recruitment, screening, informed consent, data collection, query resolution, and serving as a liaison with the sponsor.
3 months ago
INSIGHT Surgical Hospital
The Clinical Research Coordinator Assistant supports the CRC, administrative staff, and principal investigators by overseeing clinical study details, ensuring compliance with regulations, and assisting with communications between sponsors and institutes. Key duties include performing study start-up tasks, executing recruitment plans, maintaining study documentation, collecting data, and performing technical study procedures like phlebotomy.
The Clinical Research Coordinator will support principal investigators, act as a liaison between sponsors and the institute, and oversee the details of clinical studies, ensuring compliance with review boards and regulations across multiple research projects. Key duties include providing technical support, directing trial operations, managing enrolled patients, maintaining regulatory documents, and reporting adverse events to all governing bodies.
Rovia Clinical Research
This role involves managing the day-to-day operations of clinical studies, ensuring execution aligns with protocols, GCP, and SOPs, including coordinating startup activities, overseeing facility issues, and leading site meetings. Responsibilities also include monitoring enrollment progress, ensuring timely data entry into platforms like EDC, leading study visits, and providing guidance and training to site research staff.
$55,000 - $70,000 / YEAR
Profound Research
The Clinical Research Coordinator will manage all clinical trial activities under supervision, ensuring compliance with protocols, laws, and regulations. Key duties include leading trial implementation from start-up to follow-up, training staff, managing documentation, and reporting adverse events.
