Clinical Research Coordinator

Job Title: Clinical Research Associate (CRA)

Job Summary

We are seeking a detail-oriented and motivated Clinical Research Associate to oversee and monitor clinical trials. The ideal candidate will ensure studies are conducted in compliance with regulatory requirements, protocols, and ethical standards while maintaining data accuracy and patient safety.

Key Responsibilities

• Monitor and manage clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory guidelines
• Conduct site initiation, monitoring, and close-out visits
• Verify accuracy and completeness of clinical data (source data verification)
• Ensure proper documentation and maintenance of trial master files (TMF)
• Collaborate with investigators, site staff, and cross-functional teams
• Identify, report, and follow up on adverse events and protocol deviations
• Train site personnel on study protocols and procedures
• Prepare monitoring reports and maintain study records
  
  

Qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field
• Prior experience in clinical research or clinical trials preferred
• Strong understanding of GCP, ICH guidelines, and regulatory requirements
• Excellent organizational, analytical, and communication skills
• Ability to travel to clinical trial sites (if required)
  
  

Skills & Competencies

• Attention to detail and problem-solving ability
• Time management and multitasking skills
• Strong interpersonal and teamwork abilities
• Proficiency in clinical trial management systems (CTMS) and MS Office
• Ethical mindset with a commitment to patient safety
  
  

Work Environment

• Combination of office-based and on-site monitoring work
• May require travel depending on study requirements
• Fast-paced, deadline-driven environment
  
  

Career Growth Opportunities

• Senior Clinical Research Associate
• Clinical Trial Manager / Project Manager
• Regulatory Affairs Specialist
• Clinical Operations Lead