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IQVIA
Overview
The technician will be responsible for entering concomitant medications, preparing investigational products according to protocol, and compounding IV and oral agents adhering to USP standards. Key duties also involve managing drug inventory documentation and providing administrative support for audits and SOP development.
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Compensation
$33,000 - $82,600 / YEAR
Posted
4 days ago
United Urology Group
The Research Coordinator will screen, enroll, and follow study subjects for clinical trials, ensuring protocol compliance and monitoring. Responsibilities include conducting clinical trials, enrolling subjects, and managing follow-up procedures.
$27 - $31 / HOUR
24 days ago
University of Chicago
The Clinical Research Nurse coordinates and conducts clinical research trials for the Irritable Bowel Disease Program, including screening patients and obtaining informed consent. They perform clinical study visits, administer medications, and serve as a liaison between investigators, patients, and regulatory groups.
$70,000 - $100,000 / YEAR
Fortrea
The Physician Assistant provides clinical expertise and support for Phase I clinical trials, including performing physical examinations and participant assessments. The role involves acting as a technical advisor to clinical teams and ensuring compliance with FDA, GCP, and ICH regulations.
Salary not listed
29 days ago
USPI
The RN is responsible for preparing patients for procedures and managing their recovery in Phase II. This includes monitoring vital signs, administering medications, and coordinating a safe discharge process.
Northside Hospital Inc.
The Registered Professional Nurse independently plans and provides professional nursing care to patients. All care must be delivered in accordance with physician orders, established guidelines, and the Georgia Nurse Practice Act.
1 month ago
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Coordinator will participate in and coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
$46,500 - $67,046 / YEAR
City of Hope
The Clinical Nurse III will provide specialized infusion care to oncology patients within the Phase I clinic. They are responsible for applying the nursing process, maintaining professional standards, and adhering to organizational ethics and safety guidelines.
CenExel
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and performing data entry. They also assist with participant assessments, scheduling, and the facilitation of study monitoring visits.
$20 - $22 / HOUR
2 months ago
HUCKEYE HEALTH SERVICES LLC
The Clinical Research Coordinator manages complex clinical trials including drug, device, and biologic studies across all phases. They work closely with physicians and stakeholders to ensure compliance with Good Clinical Practice and FDA regulations.
$48 / HOUR
The role involves maintaining full knowledge of laboratory procedures, assisting the manager with site preparation, and managing laboratory documentation like harvest logs and sample manifests. Responsibilities also include obtaining, processing, and properly storing study samples according to protocol and ensuring freezer/refrigerator temperatures are maintained.
$20 - $21 / HOUR
The role involves executing laboratory procedures according to protocol, assisting the laboratory manager with site preparation, and maintaining detailed logs for sample handling and inventory. Responsibilities also include obtaining, processing, and properly storing biological samples while ensuring equipment and storage temperatures are maintained.
The role is responsible for assisting in coordinating clinical trials while strictly adhering to ICH, GCP, protocol, and company guidelines, managing all aspects of patient involvement from initiation to completion. Duties include organizing research information, observing subjects, scheduling data collection, documenting adverse events, and performing safety and efficacy assessments as required.
$30 - $33 / HOUR
The role is responsible for administering various clinical and neurocognitive test evaluations and interviews/ratings on study participants according to the protocol, including assessing cognitive, neuropsychological, behavioral, and functional status. Essential duties involve conducting clinical rating scales to confirm diagnoses, assisting the Principal Investigator (PI) in maintaining data integrity, and ensuring continuity of data collection among rating staff.
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.
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution for all Case Report Forms (CRFs).
$20 - $23 / HOUR
This role provides direct support to Clinical Research Coordinators to achieve protocol-specific study goals while strictly adhering to all relevant guidelines and policies. Key duties involve creating and maintaining patient charts, managing study supplies, timely data entry and query resolution, and assisting with participant assessments and scheduling.
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution for CRFs.
This role involves performing select diagnostic testing across laboratory disciplines like hematology, urinalysis, and chemistry, requiring minimal interpretation. Essential duties include maintaining laboratory logs, monitoring sample storage temperatures, preparing supplies, and ensuring strict adherence to clinical research regulations and SOPs.
The Research Assistant II provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, conducting specific assessments, and timely completion of data entry and query resolution for CRFs.
