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ICON plc
Overview
Support the design, implementation, and management of clinical trials by coordinating site initiation, patient recruitment, and data collection. Maintain comprehensive study documentation and collaborate with cross-functional teams to ensure adherence to protocols and regulatory guidelines.
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Compensation
Salary not listed
Posted
6 days ago
Serve as the primary contact between investigational sites and sponsors while conducting various site visits including selection, initiation, and close-out. Ensure site compliance with ICH-GCP and regulations while managing data quality and patient safety reporting.
$91,336 - $114,170 / YEAR
7 days ago
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 driving high-quality data entry.
$110,520 - $138,150 / YEAR
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with regulations. Oversee patient safety, drug accountability, and data quality while collaborating with cross-functional clinical teams.
KenCrest
Provide care, supervision, and habilitation to individuals with intellectual and developmental disabilities across various residential settings. Act as a caregiver and life coach to promote independence through assistance with daily living activities and community integration.
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.
Serve as the primary contact between investigational sites and sponsors while conducting various site visits including initiation and close-out. Ensure site compliance with ICH-GCP and regulations while managing data queries and patient safety reporting.
8 days ago
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 quality and site documentation.
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.
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.
Support the design, implementation, and management of clinical trials by coordinating site initiation and patient recruitment. Maintain comprehensive study documentation and collaborate with cross-functional teams to ensure regulatory compliance and data accuracy.
9 days ago
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.
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for cardio and obesity trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
14 days ago
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance and data integrity while collaborating with investigators to maintain high-quality clinical data.
16 days ago
22 days ago
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. It also requires collaborating with investigators and performing data review to maintain high-quality clinical data.
The CRA 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.
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.
