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This is a remote position.

Candidates should possess an Associate's or Bachelor's degree in one of the following disciplines:

• Psychology
  
• Life Sciences
  
• Biology
  
• Biomedical Science
  
• Public Health
  
• Health Sciences
  
• Nursing
  
• Healthcare Administration
  
• Medical Laboratory Science
  
• Related scientific or healthcare disciplines
  

• Associate's or Bachelor's degree in a relevant field.
  
• Clinical research experience preferred
  
• Strong organizational and time management skills.
  
• Excellent written and verbal communication skills.
  
• High attention to detail.
  
• Proficiency with Microsoft Office (Excel, Word, Outlook, and PowerPoint).
  
• Ability to manage multiple priorities in a fast-paced environment.
  
• Working knowledge of ICH-GCP guidelines and clinical research processes is preferred.
  

• Support the day-to-day coordination of clinical trials.
  
• Maintain and organize Trial Master File (TMF) documentation.
  
• Assist with regulatory document collection and tracking.
  
• Coordinate communication with clinical sites, sponsors, and vendors.
  
• Track study milestones, deliverables, and timelines.
  
• Review study documentation for completeness and accuracy.
  
• Support investigator meetings and study start-up activities.
  
• Assist with data management and query resolution.
  
• Ensure compliance with Good Clinical Practice (ICH-GCP), company SOPs, and regulatory requirements.
  
• Prepare reports and maintain accurate study records.
  

• Competitive hourly compensation
  
• Flexible contract assignment
  
• Opportunity to gain experience supporting clinical trials
  
• Potential for contract extension based on business needs and performance