Clinical Research Coordinator
- 401(k) matching
- Competitive salary
- Health insurance
- Paid time off
- Vision insurance
- 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.
- Preferred: 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.
- Preferred: Bilingual in English and Spanish.
- Must be local to Orange County, CA – this is not a remote position.
- Medical, Dental, and Vision Insurance
- 401(k) with company match
- Paid Time Off (PTO)
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