Freelance Clinical Research Associate (m/f/d) (0.5 FTE)

EPM Scientific are currently partnered with a mid sized CRO client running oncology clinical trials in Spain at the moment. They are seeking a Freelance Clinical Research Associate to support their clinical operations team due to temporary absence of a member. See a short summary below:

Contract Conditions:

• Start date: March
• Location: Spain
• Contract Type: Freelance, 0.5 FTE, 6 Months Contract
• Language: English, Spanish
• Project: Oncology (Phase II)

Key Responsibilities:

• Conduct site monitoring visits (pre-study, initiation, routine, and close-out) to ensure compliance with protocol, GCP, and regulatory requirements.
• Serve as the primary point of contact for investigator sites, ensuring high-quality data collection and patient safety.
• Support site selection, feasibility assessments, and start-up activities.
• Identify and resolve site-level issues, escalating risks as needed to ensure timely trial delivery.
• Maintain accurate and timely documentation of monitoring activities and site communications.
• Contribute to continuous process improvement and best practices in clinical operations.

Requirements:

• Bachelor's or Master's degree in Life Sciences or related field preferred.
• Strong (5+ years of experience preferred) as a CRA.
• Strong understanding of ICH GCP, and clinical trial processes.
• Experience in Oncology clinical trials is a must.
• Excellent organizational, communication, and interpersonal skills.
• Ability to work independently and manage multiple sites in Spain.
• Willingness to travel up to 50%.