Clinical Trials & Patient Engagement

We are seeking detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trial activities, ensuring strict adherence to GCP guidelines, regulatory requirements, and study protocols. You will play a critical role in coordinating all aspects of clinical research — from participant recruitment to data management and compliance monitoring — to support the delivery of groundbreaking medical advancements.

This is an exciting opportunity to work at the intersection of healthcare innovation, patient care, and research excellence in a collaborative, fast-paced environment.

• Coordinate and manage the day-to-day operations of clinical studies
• Recruit, screen, and consent eligible study participants in accordance with IRB-approved protocols
• Maintain accurate and up-to-date source documentation and electronic data capture (EDC) systems
• Monitor patient safety, schedule study visits, and ensure protocol adherence
• Liaise with principal investigators, sponsors, and ethics committees
• Prepare regulatory documentation, site initiation, and close-out reports
• Track study progress and submit timely updates to stakeholders
• Ensure quality assurance and compliance with ICH-GCP, MHRA, and institutional regulations

• In-depth knowledge of GCP, clinical research regulations, and ethical standards
• Experience with clinical data collection, source documentation, and informed consent processes
• Proficiency with electronic data capture systems (e.g., REDCap, Medidata, or similar)
• Strong organizational and time management skills
• Excellent communication and interpersonal abilities
• Detail-oriented and able to handle multiple trials simultaneously

• Bachelor’s degree in Life Sciences, Nursing, or Health Sciences
• ACRP or SOCRA certification
• Previous experience in oncology, cardiology, or rare disease clinical trials
• Familiarity with clinical trial software platforms and regulatory submissions

• Competitive salary with annual performance bonuses
• Training and career development in clinical operations and trial management
• Private health insurance and pension plan
• Supportive work environment with flexible working options
• Work with a cross-disciplinary team of clinical and research experts