Clinical Research Coordinator

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The Clinical Research Coordinator (CRC) will play a key role in managing studies from initiation through completion of the final study report. The CRC is responsible for ensuring quality, compliance, and efficiency in the conduct of clinical trials.

• Manage clinical studies from placement through study closeout.
• Oversee daily trial operations to ensure protocol adherence and data integrity.
• Maintain regulatory compliance with Good Clinical Practice (GCP) and ICH guidelines.
• Coordinate study visits, track enrollment, and ensure accurate documentation.
• Anticipate and coordinate study needs proactively.
• Resolve issues through strong troubleshooting and conflict‑resolution skills.
• Collaborate with investigators, sponsors, and clinical staff to support trial success.

• Minimum of 2 years of clinical research experience.
• In‑depth knowledge of clinical trial processes, GCP, and ICH guidelines.
• Strong interpersonal and communication skills.
• Exceptional organizational and planning abilities with strong attention to detail.
• Proven ability to anticipate study needs and coordinate effectively.
• Skilled in troubleshooting and conflict resolution.
• Bilingual in English and Spanish (preferred).
• Must be local to Victorville & Barstow area – this is not a remote position.

• Medical, Dental, and Vision Insurance
• 401(k) with company match
• Paid Time Off (PTO)