This is a fully remote position, open to applicants in Belgium, +1 more country.

📋 Description

• Oversee and manage the advancement of clinical trials at investigative locations.

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

• Coordinate the necessary activities for the setup and monitoring of studies.

• Identify and select investigators.

• Assist in preparing regulatory submissions.

• Conduct pre-study and initiation visits.

• Travel to sites for morning visits.

• Identify potential risks associated with studies and suggest mitigation strategies.

• Prepare for investigator meetings, site visits, and updates for the project team.

• Address conflicts utilizing effective resolution strategies.

⛳️ Requirements

• Degree in life sciences and/or equivalent experience.

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

• Experience in site management or equivalent in clinical research.

• Proven experience in managing oncology studies.

• Exceptional communication and organizational skills.

• Strong team-oriented mindset.

• Demonstrated commitment to a client-focused approach.

• Willingness to travel domestically, including overnight stays, for approximately 50–60% of the time.

• Proficiency in English and Dutch.

• Candidates must have legal authorization to work in the country of employment without requiring employer sponsorship.