Clinical Research Coordinator

Green Life Science; San Francisco (CA); On-site; USD 65,000 - 95,000; Full time

Job summary

Green Life Science in San Francisco is seeking an experienced Clinical Research Coordinator to manage the day-to-day delivery of clinical studies across multiple therapeutic areas at a site.

The ideal candidate has hands-on clinical skills including phlebotomy, a solid grasp of GCP and study protocols, and the ability to coordinate patient visits, support recruitment, maintain study documentation, and collaborate with investigators and sponsors.

Qualifications

• Hands-on clinical skills including phlebotomy and patient-facing procedures.
• Broad clinical trial experience across multiple study Phases and therapeutic areas.

Responsibilities

• Serve as the main contact for study participants and Sponsor/CRO representatives.
• Coordinate patient visits and support recruitment and retention.
• Maintain study documentation and ensure regulatory compliance.
• Collaborate with investigators and sponsors to support data quality and participant safety.
• Manage multiple studies and competing priorities with strong attention to detail.

Skills

Phlebotomy

GCP knowledge

Patient-facing procedures

Study coordination

Organization & multitasking

Job description

Looking for an experienced Clinical Research Coordinator from a clinical research site, with a strong track record of managing the day to day delivery of clinical studies across a broad range of therapeutic area.

Ideal Candidate -

• Strong hands on clinical skills, particularly phlebotomy, with confidence performing patient facing procedures.
• Broad clinical trial experience across multiple study phases and therapeutic areas.
• Strong understanding of GCP, study protocols, patient safety, and regulatory requirements.
• Comfortable coordinating patient visits, supporting recruitment and retention, maintaining study documentation, and working closely with investigators and sponsors.
• Highly organised, detail oriented, and able to manage multiple studies and competing priorities effectively.

The CRC will be the main point of contact for study participants and Sponsor/CRO representatives, working closely with investigators on participant safety and data quality. The site says CRCs typically see 3–5 patients per day, with higher volumes on heavily recruiting studies.