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

• 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
  

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