Senior Clinical Research Associate role at a global CRO supporting oncology and hematology studies across Spain. Responsibilities include site monitoring, protocol compliance, patient safety oversight, and mentoring junior staff. Based remotely with approximately 8–10 travel days monthly to investigative sites.

Responsibilities

- Lead site qualification, initiation, interim monitoring, management, and close-out in compliance with protocols and regulations
- Conduct source document verification, review CRFs, and resolve data queries to protect patient safety and data integrity
- Mentor and coordinate CRAs on general studies; provide training and accompanied site visits
- Develop monitoring plans, study tools, and training materials; review site visit reports




- Partner with study teams to evaluate site performance and support protocol adherence across investigative sites

Requirements

- MD, PharmD, MSPH, or equivalent pharmacy degree with 3+ years CRA experience
- Or bachelor's degree in medical/biological/health science with 5+ years CRA experience
- Or associate degree/nursing qualification with 7+ years CRA experience
- Strong knowledge of FDA, EU regulations, ICH Guidelines, and GCP
- Therapeutic area expertise in two to three areas
- Proficiency in Microsoft Office, IxRS, and EDC systems
- Valid passport and driving license; fluency in English and local Spanish language

📌 Senior Clinical Research Associate (España)
🏢 Worldwide Clinical Trials
📍 España