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

📋 Description

• Oversee and take ownership of the advancement of clinical trials at investigative sites.

• Ensure that clinical trials are executed, documented, and reported according to protocol, SOPs, ICH-GCP, and all relevant regulations and standards.

• Organize all essential activities necessary to initiate and oversee a study (e.g., identifying investigators; assisting with regulatory submissions, conducting pre-study and initiation visits, etc.)

⛳️ Requirements

• Bachelor's degree or equivalent experience.

• At least 2 years of experience as a CRA in either a CRO or the pharmaceutical/biotech sector, or equivalent relevant experience and/or demonstrated competencies.

• Experience in site management or equivalent in clinical research.

• Experience in oncology monitoring.

• Willingness to travel domestically, including overnight stays, which may require approximately 50-60% travel commitment.

• Proficiency in English and, for non-English speaking countries, the local language of the country where the position is based.

• Candidates must be residing in Madrid or Barcelona.