Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
Phoenix
Arizona
1222 live openings
Indianapolis
Indiana
1164 live openings
Detroit
Michigan
1158 live openings
Atlanta
Georgia
1156 live openings
Legal
VitalHires helps educators discover verified school and district opportunities. Confirm compensation, credentials, and deadlines on the official hiring site before applying.
ICON plc
Overview
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.
Quick view →
Compensation
$110,520 - $138,150 / YEAR
Posted
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
IQVIA
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 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
Glaukos
The CRA is responsible for assessing, training, and monitoring clinical research sites to ensure data integrity and protocol compliance. This includes conducting site visits, managing investigator relationships, and overseeing the accountability of investigational products.
$73,600 - $85,000 / YEAR
The University of Alabama
Provides research support for the Healthy Brain and Child Development Study, including participant recruitment, retention, and guidance. Responsible for collecting data via MRI, EEGs, cognitive assessments, and bio-specimens while tracking community resource usage.
$21 - $27 / HOUR
10 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
11 days ago
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.
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.
17 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.
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.
The Senior CRA is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They also collaborate with site staff and contribute to the preparation of study documentation and clinical study reports.
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA will collaborate with site staff and perform data review to maintain high-quality clinical trial documentation.
You will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. This involves conducting site visits, collaborating with cross-functional teams, and providing training to site staff to ensure successful trial execution.
You will conduct clinical trial monitoring activities, including site visits and data review to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while contributing to the preparation of essential study documentation.
The Senior CRA oversees clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They conduct site visits, manage data collection, and provide training to site staff to ensure successful trial execution.
The Senior CRA oversees clinical trial monitoring activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They also collaborate with cross-functional teams and provide training to site staff to facilitate successful trial execution.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with site staff and investigators while performing data review to maintain high-quality clinical documentation.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. This includes conducting site visits, collaborating with cross-functional teams, and providing training to site staff to ensure successful trial execution.
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data entry and site documentation.
