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IQVIANew
Overview
Responsible for the preparation, scanning, and maintenance of electronic and paper medical records for a clinical trial practice. The role involves gathering patient records from various sources and ensuring all releases of information comply with HIPAA guidelines.
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Compensation
$25,900 - $64,800 / YEAR
Posted
New
ICON plcNew
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.
$19 / HOUR
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 Sr. CRA is responsible for managing investigative sites and performing monitoring activities throughout the clinical trial lifecycle to ensure data integrity and subject safety. Key duties include conducting site visits, managing essential documents, and ensuring compliance with protocols and regulatory standards.
$110,520 - $138,150 / YEAR
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
Design and execute experiments for method development in flow cytometry and ligand binding assays. Provide scientific leadership through mentoring junior staff, reviewing data, and communicating project status to clients and management.
3 days ago
IQVIA
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
4 days ago
Perform in-home diagnostic services including phlebotomy, EKGs, and macular edema screenings for patients. Manage clinical supplies, transport specimens to laboratories, and maintain accurate visit documentation.
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 and report adverse events.
Perform in-home diagnostic services including blood specimen collection, EKGs, and macular edema screenings. Manage clinical supplies and collaborate with the coordination team to submit accurate visit paperwork.
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 phlebotomy, EKGs, and macular edema screenings for patients. Manage clinical supplies and coordinate with the clinical team to submit accurate visit-related paperwork.
Perform in-home diagnostic services including phlebotomy, EKGs, and macular edema screenings. Manage clinical supplies and coordinate with the clinical team to submit visit-related paperwork and report adverse events.
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
The Clinical Research Nurse is responsible for coordinating and conducting clinical trial procedures according to protocol requirements. This includes performing technical clinical tasks, documenting patient data, and collaborating with interdisciplinary teams to ensure trial compliance.
10 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.
16 days ago
The Medical Research Associate is responsible for greeting clinical research volunteers and performing vital sign assessments and phlebotomy procedures according to study protocols. They also provide personalized care to study subjects and ensure their comfort throughout the research process.
