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ICON plc
Overview
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.
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Compensation
$91,336 - $114,170 / 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
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
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 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 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.
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.
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.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Conduct site visits to assess performance, resolve issues, and collaborate with cross-functional teams for accurate data reporting.
The Clinical Research Associate serves as the primary point of contact for investigational sites, ensuring compliance with ICH-GCP and regulatory standards. They are responsible for conducting site visits, monitoring patient safety, managing data integrity, and overseeing drug accountability.
The Clinical Research Associate is responsible for conducting site qualification, monitoring, and close-out visits to ensure protocol compliance and patient safety. They also collaborate with site staff to facilitate study conduct and perform data review to maintain high-quality clinical data.
25 days ago
Fortrea
Responsible for all aspects of study site monitoring, including routine visits, close-outs, and site management for oncology clinical trials. Ensures data integrity, patient protection, and adherence to protocol and regulatory requirements.
$115,000 - $140,000 / YEAR
1 month ago
Responsible for all aspects of clinical site monitoring, including routine visits, close-outs, and site management. Ensures patient protection, data integrity, and adherence to study protocols and regulatory requirements.
Theradex Oncology
The Clinical Research Associate will conduct site monitoring visits, including qualification, initiation, routine, and close-out visits to ensure protocol compliance and data integrity. They will also act as a liaison between study sites and the project team while managing site documentation and safety reporting.
$75,000 - $145,000 / YEAR
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA is responsible for data review, query resolution, and contributing to study documentation and reports.
The Clinical Research Associate serves as the primary point of contact for investigational sites, conducting site visits to ensure compliance with ICH-GCP and regulatory standards. They are responsible for monitoring patient safety, managing site documentation, and overseeing drug accountability throughout the clinical trial process.
Platinum Dermatology Partners LLC
Responsible for the administrative and clinical execution of research studies, including subject recruitment, screening, and data management. Provides direct support to Principal Investigators by assisting with medical procedures and ensuring compliance with FDA and IRB guidelines.
$28 - $31 / HOUR
IQVIA
The Clinical Research Associate performs site monitoring visits to ensure study protocols, regulations, and sponsor requirements are strictly followed. They manage site progress, including recruitment, data integrity, and regulatory documentation to ensure high-quality study execution.
$71,900 - $189,000 / YEAR
