Jobs at Syneos Health

Perform site monitoring, manage clinical data compliance, document activities, ensure regulatory compliance, support patient recruitment, and liaise with project teams.

The SCRA I is responsible for site management, compliance monitoring, and supporting clinical study activities while ensuring regulatory adherence and data integrity.

The SCRA I is responsible for site monitoring and management, ensuring compliance with regulations, managing site documents, and supporting study activities throughout the lifecycle.

The CRA I conducts site management activities, ensuring compliance with regulations, oversees data integrity, and assists in subject recruitment and retention throughout clinical study lifecycles.

The CRA I will manage site qualification, initiation, compliance monitoring, and documentation activities, ensuring protocol adherence in clinical trials. Responsibilities include supporting study lifecycles and training site staff while maintaining effective communication with project teams and site personnel.

The CRA I performs site qualification, monitoring, and management activities ensuring compliance with regulations and protocols while facilitating effective communication between sites and the project team.

Responsible for site management activities including site qualification, monitoring, compliance assessments, and documentation as per regulatory standards and guidelines. Serves as a liaison between project site personnel and supports audit readiness and subject recruitment.

The CRA II/ SCRA performs site management tasks including qualification, initiation, monitoring, and close-out visits while ensuring compliance with regulations. They manage data integrity, assess subject safety, and engage in project communications, aiming to meet study objectives effectively.

The Sr CRA will oversee clinical study site management including site qualification, monitoring, and compliance with regulatory standards while supporting project timelines and objectives.

The role involves site management activities in clinical trials, ensuring compliance with regulations, data accuracy, and effective communication with site personnel. It supports patient safety and recruitment, while managing site activities and documentation throughout the study lifecycle.

The CRA II- SCRA conducts site qualification and management activities, ensuring compliance with regulatory guidelines, supporting patient recruitment, and documenting site activities.

The CRA II- SCRA will oversee site activities, ensuring compliance with regulatory standards while performing monitoring, data verification, and site management throughout the study lifecycle.