Senior Clinical Research Associate – Oncology, Hematology

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Perform site qualification, initiation, interim monitoring, site management, and study close-out visits.

• Provide mentorship and support to less seasoned CRAs and site personnel when necessary.

• Record site visit observations through detailed written reports.

• Evaluate, oversee, and instruct study site staff on adherence to protocols.

• Analyze study subject safety data and informed consent documentation.

• Execute source document verification to ensure compliance, patient safety, and data integrity.

• Review Case Report Forms (CRFs) utilizing paper or electronic data capture systems.

• Aid sites in resolving data queries.

• Update site-specific documentation for inclusion in the Trial Master File (TMF).

• Ensure adherence to investigational product receipt, accountability, and proper return or disposal.

• Conduct joint site visits for the assessment or training of other CRAs as required and appropriate.

⛳️ Requirements

• Exceptional interpersonal, verbal, and written communication abilities in English.

• Outstanding organizational skills with a keen eye for detail.

• Capability to work independently with minimal supervision.

• Proficient in Microsoft Office, Clinical Trial Management Systems (CTMS), and Electronic Data Capture (EDC) systems.

• Over 5 years of experience as a Clinical Research Associate.

• Bachelor’s degree or RN/BSN in Nursing.

• Willingness to travel as needed.

🏝️ Benefits

• Equal employment opportunities without regard to protected characteristics.

• A diverse and inclusive workplace.

• Supportive and collaborative teams.

• Accessible and hands-on leadership.

• Opportunities for professional growth and development.

• Mentorship and guidance opportunities available.