National Institute of Clinical Research, Inc.
Clinical Research Coordinator
National Institute of Clinical Research, Inc., Garden Grove, California, United States, 92641
Job Description
Benefits :
401(k) matching
Competitive salary
Health insurance
Paid time off
Vision insurance
Position:
Clinical Research Coordinator (CRC) Location: Garden Grove, CA (On-site, Full-time) The National Institute of Clinical Research (NICR) is an independent, multi-site Site Management Organization (SMO) conducting Phase I-IV clinical trials since 1996. With over 500 successful trials completed, we are dedicated to delivering the highest quality in clinical research. Position Summary 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. Key Responsibilities Manage clinical studies from start to finish, including study initiation, conduct, and 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. Proactively anticipate and coordinate study needs. Resolve issues through troubleshooting and conflict-resolution skills. Collaborate with investigators, sponsors, and clinical staff to support trial success. Requirements Minimum of 2 years of clinical research experience (preferred). 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 Orange County, CA — this is not a remote position. Additional Benefits Medical, Dental, and Vision Insurance 401(k) with company match Paid Time Off (PTO)
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Clinical Research Coordinator (CRC) Location: Garden Grove, CA (On-site, Full-time) The National Institute of Clinical Research (NICR) is an independent, multi-site Site Management Organization (SMO) conducting Phase I-IV clinical trials since 1996. With over 500 successful trials completed, we are dedicated to delivering the highest quality in clinical research. Position Summary 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. Key Responsibilities Manage clinical studies from start to finish, including study initiation, conduct, and 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. Proactively anticipate and coordinate study needs. Resolve issues through troubleshooting and conflict-resolution skills. Collaborate with investigators, sponsors, and clinical staff to support trial success. Requirements Minimum of 2 years of clinical research experience (preferred). 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 Orange County, CA — this is not a remote position. Additional Benefits Medical, Dental, and Vision Insurance 401(k) with company match Paid Time Off (PTO)
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