Senior Clinical Research Associate

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

📋 Description

• Accountable for site qualification, initiation, interim monitoring, management of sites, and conducting study close-out visits.

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

• Record findings from site visits through comprehensive written reports.

• Evaluate, supervise, and instruct study site personnel on adherence to protocols as needed.

• Analyze study subject safety data and informed consent documentation.

• Perform source document verification to ensure compliance, safeguard patient well-being, and verify data accuracy.

• Examine CRFs utilizing paper or electronic data capture systems and assist sites in resolving data queries.

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

• Guarantee site adherence to investigational product receipt, accountability, and return or destruction protocols.

• Conduct accompanied site visits for the assessment or training of fellow CRAs as requested and deemed appropriate.

⛳️ Requirements

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

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

• Required experience in Oncology, Hematology, and Neurology.

• Must be willing to travel.

🏝️ Benefits

• Health insurance.

• Retirement plans.

• Paid time off.

• Flexible work arrangements.

• Opportunities for professional development.