Job Title: Clinical Research Coordinator
About the Role:
We are seeking a detail-oriented and proactive Clinical Research Coordinator (CRC) to assist with essential study-related tasks on a flexible, part-time basis. This role is perfect for someone who is highly organized, self-directed, and looking to contribute to clinical research in a supportive, focused capacity.
Key Responsibilities:
- Assist with study documentation and regulatory compliance
- Support data entry and maintenance in EDC systems
- Help schedule and track patient visits or study milestones
- Coordinate with study sponsors, investigators, and research staff
- Ensure accurate filing and organization of study documents
- Assist with IRB communications and submissions, if needed
Requirements:
- Previous experience in clinical research coordination
- Familiarity with regulatory requirements (GCP, IRB, FDA)
- Strong attention to detail and ability to manage tasks independently
- Excellent communication and organizational skills
- Proficient in using EDC systems, Microsoft Office, and email
Preferred Qualifications:
- CCRC or ACRP certification
Location: Houston, TX
Schedule: 5 hours per week
Start Date: ASAP
Employment Type: Part-Time / Contract