Clinical Research Coordinator

Job Description

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.

Job Responsibilities

• 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
  

Requirements

Required Skills

• 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
  

Desired Skills

• Bachelors 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
  

Benefits

Job Benefits

• 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