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

📋 Description

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

• Ensure that clinical trials are executed, documented, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all relevant regulations and standards.

• Coordinate all essential activities necessary to establish and oversee a study (e.g., identifying investigators; assisting in the preparation of regulatory submissions, conducting pre-study and initiation visits, etc.).

⛳️ Requirements

• Bachelor's degree or equivalent experience.

• A minimum of 2 years as a Clinical Research Associate (CRA) in a Contract Research Organization (CRO) or in the pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies.

• Experience in site management or a comparable role in clinical research.

• Experience in oncology monitoring.

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

• Proficiency in English, and for positions in non-English speaking countries, fluency in the local language.

• Applicants must be residing in Madrid or Barcelona.