Clinical Research Coordinator

📋 Description

• Coordinate studies from start-up to close-out, including feasibility and recruitment.
• Manage regulatory submissions, renewals, amendments, and IRB queries.
• Independently manage all trial phases with GCP and SOP compliance.
• Recruit, screen, consent, and enroll participants per protocol.
• Maintain study docs: CRFs, EDC, and source documents.
• Perform phlebotomy and handle specimens per IATA standards.

🎯 Requirements

• Strong communication, organizational, and problem-solving skills.
• Proficient in phlebotomy, including venipuncture and specimen processing.
• Able to work independently and manage multiple trials concurrently.
• Knowledge of clinical research processes, FDA regs, and IRB compliance.

🎁 Benefits

• Inclusive, patient-centered clinical research that improves accessibility.
• Collaborative team delivering virtual-first clinical research at scale.
• Growth opportunities within an established startup with industry veterans.