Senior Clinical Research Associate

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

📋 Description

• In the role of Senior CRA, you will be at the forefront of communication with project stakeholders, ensuring that timelines, targets, and standards of clinical research projects across a range of therapeutic areas are met.

• You will establish and nurture relationships with clinical sites and investigators.

• Your primary focus will be on the rights, safety, and well-being of subjects, along with ensuring quality data compliance.

• Your responsibilities will encompass conducting and documenting various onsite monitoring visits, facilitating the study startup phase, carrying out CRF reviews, verifying source documents, and resolving queries.

⛳️ Requirements

• A BSc or MSc in Life Sciences (or a comparable field), or an equivalent combination of education, training, and experience.

• Proven independent on-site monitoring experience within the Netherlands.

• Demonstrated experience in conducting all types of monitoring visits in Phase II and/or III studies.

• Excellent written and verbal communication abilities.

• Proficiency in Dutch and English.

• Experience in supporting Oncology studies is advantageous, though not mandatory.

• Advanced proficiency in MS Office applications.

• A full and clear driver's license, along with the willingness to travel.

• Essential skills include communication, collaboration, and problem-solving.

• Ability to manage multiple tasks and thrive in a dynamic team environment.

🏝️ Benefits

• Take the right step and elevate your career to new heights.

• Become part of a company that prioritizes its people and invests in their professional growth and success.

• Our recruitment process is uncomplicated and transparent, with support provided at every stage.

• We will offer guidance and support with information, ensuring your experience is as seamless as possible.