Senior Clinical Research Associate – Contractor

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

📋 Description

• Conduct Pre-Study, Initiation, Interim, and Close-Out monitoring visits, either on-site or remotely.

• Ensure that the facilities and staff at investigational sites are suitable for the execution of the study.

• Identify and verify the qualifications, resources, facilities, equipment, and personnel of investigators throughout the duration of the study.

• Provide training to investigational site staff as needed.

• Oversee clinical research activities in Belgium, the Netherlands, and potentially France.

⛳️ Requirements

• A college or university degree in Life Sciences or an equivalent combination of education, training, and experience.

• Proficiency in French, Flemish, and English.

• Significant experience in on-site monitoring for phase 2/3 trials.

• Preferably, experience with complex trials in oncology or rare diseases.

• Capability to plan, multitask, and thrive in a dynamic team setting.

• Strong communication, collaboration, and problem-solving abilities.

• Willingness to travel.

🏝️ Benefits

• Emphasis on work-life balance.

• Engage in a collaborative, international team environment.

• Opportunities for career advancement.

• Empowered to take ownership early in your role.

• Supportive team culture.

• Chance to contribute to providing safe and effective pharmaceutical treatments to patients worldwide.