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

📋 Description

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

• Ensure that clinical studies are executed, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and relevant regulations and standards.

• Organize the activities necessary to establish and monitor studies.

• Identify and select investigators.

• Assist in the preparation of regulatory submissions.

• Conduct pre-study and initiation visits.

• Contribute ideas and insights that are appreciated and can lead to positive changes within the organization.

⛳️ Requirements

• A 4-year college degree or equivalent experience is required.

• A minimum of two years as a CRA in a CRO or the pharmaceutical/biotech industry, or similar relevant experience and/or demonstrated competencies.

• Experience in site management or equivalent within clinical research.

• Background in oncology monitoring is preferred.

• Must be available for domestic travel, including overnight stays, which may account for approximately 50-60% travel commitment.

• Proficiency in English; for non-English speaking countries, fluency in the local language of the respective country is necessary.

• Candidates should reside in either Madrid or Barcelona.

• Applications should be submitted in English only.

• A graduate or postgraduate degree with a focus in a scientific or healthcare field is preferred.

• Experience in Phase I studies is a plus.

• Experience managing CAR-T/ FIH studies is preferred.

🏝️ Benefits

• High retention rates for CRAs and a fulfilling quality of life.

• A lower than average number of protocols to manage.

• Reasonable travel requirements that enhance work/life balance.

• Support from direct line management.

• An opportunity to influence and make an impact.

• Employee contributions and ideas are valued and encouraged.