Clinical Research Associate II – Sponsor Dedicated

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

📋 Description

• Perform both on-site and remote oversight of clinical research studies to ensure adherence to widely recognized clinical practices.

• Create and implement tools, procedures, and processes to guarantee quality monitoring.

• Aid in the design, execution, and delivery of processes, programs, and policies.

• Oversee specific components of projects or processes within the designated area of responsibility.

• Ensure the precise and timely documentation of monitoring activities and observations.

• Work in collaboration with cross-functional teams to facilitate clinical trial operations.

⛳️ Requirements

• A Bachelor's degree in a related discipline or equivalent experience.

• At least 2-4 years of experience in clinical research monitoring.

• Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory standards.

• Exceptional communication and interpersonal abilities.

• Proficiency in Dutch.

• Capacity to work independently and manage several priorities simultaneously.

• Competence in using clinical trial management systems and other pertinent software.

🏝️ Benefits

• We are dedicated to the growth of our employees through career development and advancement opportunities.

• Supportive and engaged line management.

• Technical and therapeutic area training.

• Peer recognition and a comprehensive rewards program.

• We are committed to fostering an inclusive culture where you can genuinely be yourself.