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.

• Offer mentoring and support to junior CRAs and site personnel.

• Record site visit observations through comprehensive written reports.

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

• Analyze study subject safety data and informed consent documents.

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

• Review Case Report Forms (CRFs) using both paper and electronic data capture systems, assisting sites with data query resolution.

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

• Guarantee site compliance with the receipt, accountability, and return or destruction of investigational products.

• Conduct accompanied site visits for assessment or training purposes for other CRAs.

⛳️ Requirements

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

• Outstanding organizational capabilities with a keen eye for detail.

• Ability to operate 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 required.

• Willingness to travel is mandatory.

🏝️ Benefits

• Equal employment opportunities.

• Diverse and inclusive workplace.

• Supportive and collaborative teams.

• Accessible and hands-on leadership.

• Opportunities for professional growth and development.