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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
The CRC manages Phase II-IV clinical studies from initiation to close-out, ensuring compliance with FDA and GCP guidelines. Key duties include conducting subject visits, managing recruitment, and maintaining accurate clinical documentation.
Salary not listed
9 days ago
The CRC manages and executes Phase I-IV clinical studies from site initiation to close-out, ensuring compliance with FDA and GCP guidelines. Key duties include conducting subject visits, managing recruitment, and maintaining accurate clinical documentation.
10 days ago
Coordinate all aspects of assigned clinical trials from site initiation through close-out, ensuring compliance with protocols and regulatory standards. Manage subject visits, recruitment, data entry, and collaboration with investigators and sponsors.
$70,000 - $80,000 / YEAR
The Clinical Research Coordinator will manage and execute Phase II-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaborating with investigators and lab teams to maintain study integrity.
The Clinical Research Coordinator manages and executes Phase I-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaboration with investigators and sponsors.
DM CLINICAL RESEARCH GROUP
The Clinical Research Coordinator II ensures quality research is conducted at investigative sites in compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines. Key duties include managing subject visits, handling data entry, and overseeing the reporting of adverse events.
11 days ago
Be Well Clinical Studies
The Sub-Investigator supports the Principal Investigator in conducting clinical trials by performing medical procedures and ensuring protocol adherence. They are responsible for subject eligibility assessments, patient safety, and maintaining high standards of data integrity.
$65 - $90 / HOUR
12 days ago
17 days ago
The Clinical Research Coordinator II ensures quality research is conducted at investigative sites following sponsor protocols, FDA regulations, and ICH/GCP guidelines. Key duties include managing subject visits, handling data entry, and overseeing the reporting of adverse events.
23 days ago
Tandem Intermediate LLC
The Clinical Rater conducts interviews and administers psychometric rating scales to evaluate research participants for clinical study enrollment. They ensure data integrity and participant safety while maintaining compliance with FDA, GCP, and ICH guidelines.
1 month ago
Tekton Research Inc
The Psychometric Rater conducts clinical interviews and psychometric rating scales on research participants to evaluate eligibility and health status. They ensure compliance with study protocols, FDA regulations, and maintain accurate source documentation while coordinating with site staff and sponsors.
