Senior Clinical Research Associate

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

📋 Description

• Accountable for site qualification, initiation, interim monitoring, management, and closing visits for studies.

• Offer mentorship and support to junior CRAs and site personnel as necessary.

• Record findings from site visits through comprehensive written reports.

• Evaluate, oversee, and educate study site personnel on adherence to protocols as needed.

• Examine study subject safety information and informed consent documents.

• Perform source document verification to ensure compliance, patient safety, and accuracy of data.

• Review Case Report Forms (CRFs) utilizing paper or electronic data capture systems and assist sites with resolving data queries.

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

⛳️ Requirements

• Minimum of 2 years’ experience as a Clinical Research Associate.

• Bachelor's degree from a four-year university or RN/BSN in Nursing.

• Required experience in Oncology and Neurology.

• Must be willing to travel.

🏝️ Benefits

• A diverse and inclusive workplace.

• Accessible and hands-on leadership.

• Supportive team environment.