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Explore live opportunities across Blue Bell, South Dakota. 26 open roles • 2 newly posted in the last 14 days.
Open jobs
26
Posted in 14 days
2
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.
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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
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
Provide technical support in molecular biology, microbiology, and immunology to support structure-based drug designs for microbial pathogens. Perform genetic analysis and culture infectious agents within BSL-2 and BSL-3 laboratory environments.
$68,616 - $85,770 / YEAR
17 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.
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.
