Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
ICON plcNew
Overview
The intern will support clinical delivery by managing essential document collection, maintaining the Trial Master File, and ensuring timely data entry into CTMS. They will also assist with risk assessment, trial material tracking, and general clinical operations tasks.
Quick view →
Compensation
$19 / HOUR
Posted
New
ICON plc
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
$91,336 - $114,170 / YEAR
2 days ago
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
Salary not listed
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
9 days ago
The Study Startup Specialist coordinates and oversees all aspects of clinical trial initiation, including managing essential document collection, regulatory submissions to bodies like IRB/EC, and tracking startup milestones to ensure sites are ready for patient enrollment on time. This role involves preparing, reviewing, and submitting regulatory documents, supporting contract/budget negotiations, and maintaining audit-ready documentation in systems like eTMF.
$70,000 - $95,000 / YEAR
Rapport Therapeutics
The Senior Clinical Trial Associate manages clinical study documentation, including the Trial Master File, to ensure inspection readiness and compliance with ICH-GCP standards. They also support the trial team with administrative tasks, vendor invoice tracking, and the preparation of essential study-related documents.
$90,000 - $110,000 / YEAR
11 days ago
AstraZeneca
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for study sites, driving performance, resolving issues, and ensuring data quality through monitoring visits and source data review.
$112,154 - $168,232 / YEAR
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for sites, driving performance, resolving study-related issues, and managing study supplies.
Care Access
Perform clinical tasks including venipuncture and biospecimen processing to support clinical trials. Handle administrative duties such as participant scheduling, data entry, and maintaining site logs.
$24 - $38 / HOUR
13 days ago
Adams Clinical
Provide foundational operational and administrative support for clinical trials, including participant screening, scheduling, and clinical procedures. Maintain accurate ALCOA+-compliant documentation and perform data entry into EDC systems to ensure audit readiness.
$22 - $25 / HOUR
The Enrollment RA supports the evaluation, triage, and enrollment of clinical trial participants while ensuring compliance with study protocols and regulatory requirements. They perform essential administrative and clinical tasks, including scheduling, data entry, and basic clinical procedures like vital signs and phlebotomy.
$18 - $24 / HOUR
The Laboratory Technician manages daily lab workflows, including specimen collection, processing, and shipping while ensuring compliance with clinical trial protocols. They also perform participant-facing clinical procedures such as phlebotomy, vital signs, and ECGs to support study visit flow.
$24 - $27 / HOUR
The Lead Study Therapist will provide support to participants throughout clinical trials and monitor dosing sessions in alignment with study protocols. They will also collaborate with the clinical team to ensure data quality and participant safety.
$60 - $70 / HOUR
Ora
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks and collaborate with project managers and investigators to execute research directives.
14 days ago
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks, manage study documentation, and collaborate with investigators to execute research directives.
The Clinical Research Coordinator I collects and organizes subject information during clinical study visits while ensuring protocol compliance. They perform technician-based tasks, manage study documentation, and collaborate with investigators and project managers.
CHOC
The Clinical Research Coordinator II provides coordinator support for multiple human subjects’ research projects, performing all core CRC responsibilities with minimal supervision. This includes assessing protocol feasibility, preparing IRB submissions, identifying participants, coordinating data/specimens, maintaining accurate study records, and managing supplies.
$31 - $51 / HOUR
15 days ago
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
$110,520 - $138,150 / YEAR
16 days ago
The Senior Clinical Research Associate will conduct site qualification, monitoring, and close-out visits while ensuring protocol compliance and data integrity. They will also collaborate with investigators and contribute to the preparation of study documentation and clinical reports.
17 days ago
The Senior Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining data integrity throughout clinical trials. They also collaborate with site staff and investigators to facilitate study conduct and prepare essential study documentation.
