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Headlands Research
Overview
The Pharmacy Technician is responsible for the safe handling, preparation, and dispensing of investigational products in accordance with study protocols and GCP regulations. They also manage pharmacy documentation, maintain inventory logs, and provide administrative support for clinical trials.
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Compensation
$22 - $26 / HOUR
Posted
4 days ago
Systimmune
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
$90,000 - $130,000 / YEAR
10 days ago
Flourish Research
The coordinator executes protocol-specified patient visits and procedures while documenting study data in accordance with GCP and FDA guidelines. They are also responsible for recruiting qualified subjects, obtaining informed consent, and reporting adverse events to sponsors and investigators.
$31 - $43 / HOUR
14 days ago
The coordinator executes protocol-specified patient visits and procedures while ensuring all study data is documented according to GCP and FDA guidelines. They are also responsible for ethical subject recruitment, obtaining informed consent, and managing trial materials.
$25 - $28 / HOUR
15 days ago
Bon Secours Mercy Health
Coordinate and manage clinical research studies within the Cancer Institute, including patient recruitment, enrollment, and data collection. Serve as a liaison between sponsoring agencies and hospital departments while ensuring adherence to study regulations and providing direct patient care.
Salary not listed
BMC Software
The Clinical Research Coordinator II manages research activities including patient recruitment, informed consent, and the processing of biological specimens. They are responsible for maintaining patient databases, entering data into electronic capture forms, and assisting with regulatory submissions and audits.
$42,500 - $59,500 / YEAR
19 days ago
The CRA II manages and oversees clinical study sites to ensure data quality and patient safety in compliance with ICH-GCP and local regulations. Key duties include performing site visits, managing patient recruitment, and maintaining the Trial Master File.
$80,000 - $110,000 / YEAR
23 days ago
Best Care
Coordinates clinical research studies including regulatory compliance, study start-up, subject follow-up, and record maintenance. Manages trial oversight, participant safety, and the handling of investigational products.
29 days ago
