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%.
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