Clinical Research Associate

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

📋 Description

• Perform qualification, initiation, monitoring, and closeout visits for research sites in alignment with the approved protocol.

• Engage with medical site personnel, including coordinators, clinical research physicians, and site staff.

• Confirm investigator qualifications, training, resources, facilities, laboratories, equipment, and personnel.

• Validate medical records and research source documentation against case report form data.

• Notify site staff of entry errors and ensure adherence to good documentation practices.

• Report protocol deviations in accordance with SOPs, GCP, and relevant regulatory requirements.

• Ensure that investigators enroll only eligible subjects.

• Review regulatory documents.

• Oversee accountability and inventory management of medical devices and investigational products/drugs.

• Verify and evaluate adverse events, serious adverse events, concomitant medications, and related illnesses.

• Analyze site patient recruitment and retention, providing suggestions for improvement.

• Complete monitoring reports and follow-up letters that summarize findings, deviations, deficiencies, and suggested compliance actions.

• Maintain strong collaboration with internal cross-functional teams at Medpace globally.

• Attend the virtual Medpace event on 14 October 2026, from 16:00 to 17:00 CEST via Microsoft Teams, if selected.

⛳️ Requirements

• Currently employed as a Clinical Research Coordinator, Clinical Research Nurse, or in an equivalent position.

• Must reside in Belgium with full work authorization.

• A minimum of a Bachelor of Science degree in a Health or Life Science-related field.

• At least 1 year of clinical research experience with direct patient interaction as a Clinical Research Coordinator, Clinical Study Coordinator, or similar role.

• Proficient in English, Dutch, and French.

• Exceptional communication and problem-solving abilities.

• Willingness to travel approximately 60-70% nationally.

• Valid driver’s license required.

• Proficiency in Microsoft® Office.

• Applications must be submitted in English.

🏝️ Benefits

• Competitive compensation programs that acknowledge and reward performance.

• Comprehensive health, wellness, retirement, and paid time off (PTO) benefits.

• Office-based culture with occasional work from home flexibility for eligible positions post-training.

• Company-sponsored social events.

• Purpose-driven work alongside physicians, scientists, and industry-leading experts.

• Collaborative work environment.

• Defined career paths with clear opportunities for advancement.

• Industry-renowned onboarding and training programs.

• Ongoing training and continuous learning opportunities.

• On-site mentorship available.

• Open channels of communication and a foundation of mutual trust.

• An environment that encourages employees to influence change, contribute ideas, and advance rapidly.