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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.
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Compensation
$19 / HOUR
Posted
New
UT Southwestern Medical Center
Provide technical assistance for preclinical research studies evaluating gene therapy in rodent models of neurological disorders. Responsibilities include conducting behavioral assays, monitoring animal health, and maintaining research rodent colonies.
Salary not listed
2 days ago
Labcorp
Perform phlebotomy services within a hospital setting to support diagnostic testing. Provide vital information to help healthcare providers make confident patient care decisions.
4 days ago
IQVIA
Deliver in-home clinical services including phlebotomy, EKGs, and macular edema screenings for patients initiating complex medication therapies. Manage clinical supply inventory and coordinate with the clinical team to submit visit-related paperwork and report adverse events.
$28 / HOUR
Deliver in-home clinical services including phlebotomy, EKGs, and macular edema screenings for patients initiating complex therapies. Manage clinical supplies and coordinate with the clinical team to submit visit-related paperwork and report adverse events.
Perform in-home diagnostic services including blood specimen collection, EKGs, and macular edema screenings. Manage clinical supplies and coordinate with the clinical team to submit visit-related paperwork accurately.
$25 / HOUR
Avalo Therapeutics
The Clinical Trial Associate will support the planning, execution, and delivery of clinical trials in compliance with regulatory standards and internal SOPs. Responsibilities include tracking study progress, managing vendor relationships, and ensuring the quality and completeness of trial documentation.
6 days ago
Terumo
The Clinical Research Coordinator provides administrative and operational support to the Clinical Research and Operations department to ensure adherence to study plans and regulatory standards. Responsibilities include managing study documentation, maintaining the electronic trial master file, and coordinating with clinical sites and vendors.
$44,900 - $61,710 / YEAR
7 days ago
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
$71,900 - $169,300 / YEAR
9 days ago
Systimmune
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
Headlands Research
Clinical Research Coordinators manage the day-to-day execution of clinical trials, including coordinating study visits and collecting data. They work directly with patients, investigators, and cross-functional teams to ensure compliance with protocols and regulatory requirements.
$45,000 - $100,000 / YEAR
American Clinical Research Services Opco LLC
The Clinical Research Coordinator manages clinical trials by overseeing subject recruitment, dosing, and data collection while ensuring regulatory compliance. They collaborate with investigators to maintain study documentation and monitor participant progress throughout the trial.
$50,000 - $67,000 / YEAR
13 days ago
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.
Perform routine and complex technical procedures in hematology while monitoring and troubleshooting laboratory instrumentation. Ensure quality patient care by reporting accurate test results and maintaining a safe work environment.
The role involves conducting routine and non-routine sample analysis in compliance with SOPs and regulatory guidelines. Responsibilities include maintaining laboratory records, performing equipment maintenance, and assisting in the validation of immunotoxicology assays.
15 days ago
Beth Israel Lahey Health
Conduct routine molecular, cell biology, and biochemistry experiments under the supervision of a principal investigator. Collect and analyze study data using basic statistics and maintain detailed records of methodologies and results.
$19 - $26 / HOUR
17 days ago
ICON plc
The Senior CRA will oversee clinical trial monitoring activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They will also conduct site visits, manage site performance, and collaborate with cross-functional teams to ensure accurate data collection.
