04/13/2026
Job Title: Clinical Research Coordinator (CRC)
Company: Vida Clinical Research
Job Type: Full-Time
Position Overview:
Vida Clinical Research is seeking a highly skilled and experienced Clinical Research Coordinator (CRC) to oversee and manage clinical trials under the direction of the Clinical Research Site Director and Principal Investigator. The ideal candidate will demonstrate strong clinical knowledge, regulatory compliance expertise, and the ability to manage multiple studies while ensuring patient safety and data integrity.
Key Responsibilities:
• Manage and coordinate 6–8 clinical trials simultaneously
• Ensure strict adherence to study protocols, Research SOPs, and Good Clinical Practices (GCP)
• Protect the rights, safety, and well-being of study participants
• Obtain and document informed consent and ensure proper patient communication
• Conduct patient visits, including vital signs, ECGs, and study-related procedures
• Collect, process, and ship laboratory specimens per protocol requirements
• Maintain accurate and complete case report forms (CRFs) in compliance with FDA guidelines
• Monitor, document, and report adverse events appropriately
• Review laboratory results and ensure physician oversight for clinical significance
• Schedule and coordinate patient visits and study procedures
• Maintain regulatory binders and essential study documentation
• Prepare for and coordinate monitoring visits
• Submit patient reimbursement requests in a timely manner
• Collaborate effectively with physicians, staff, and sponsors
Qualifications & Requirements:
• Minimum 5 years of healthcare experience (required)
• Minimum 5 years of clinical trials experience (required)
• Minimum 5 years of EMR systems experience (required)
• Strong knowledge of Good Clinical Practices (GCP), FDA regulations, and human subject protection
• Familiarity with IATA regulations for shipping biological specimens
• Excellent organizational, analytical, and problem-solving skills
• Strong written and verbal communication skills
• Ability to work both independently and in a team environment
• Bilingual (required)
• preferably CCRC certified
Education & Experience:
• Minimum of 5 years in a related healthcare position or equivalent combination of education and experience (clinical trial experience preferred)
Additional Requirements:
• Ability to interpret technical procedures, protocols, and regulatory guidelines
• Professional conduct with close attention to detail
• Willingness to travel to satellite locations as needed
Compensation:
Salary will be discussed during the interview process.
How to Apply:
Interested candidates are encouraged to email their resumes and qualifications for consideration at raveloo@vidaclinicalresearch.com.
Vida Clinical Research is committed to maintaining the highest standards in clinical research and patient care. We look forward to welcoming a dedicated professional to our growing team.