Clinical Research Coordinator Jobot
Fountain Valley, CA7 days ago
- $70,000–$75,000 Per Year
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Skills
- Cardiovascularunmatched
- Clinical Researchunmatched
- Clinical Supportunmatched
- Clinical Trialunmatched
- Communication Skillsunmatched
- Conflict Resolutionunmatched
- Data Qualityunmatched
- Dental Insuranceunmatched
- Detail Orientedunmatched
- Documentationunmatched
- English Languageunmatched
- GCP (Good Clinical Practices)unmatched
- Geriatricsunmatched
- Healthcareunmatched
- Healthcare Qualityunmatched
- Identify Issuesunmatched
- Infectious Diseasesunmatched
- Interpersonal Skillsunmatched
- Maintain Complianceunmatched
- Multilingualunmatched
- Nephrologyunmatched
- Operationsunmatched
- Organizational Skillsunmatched
- Phase I Clinical Trialsunmatched
- Phase IV Clinical Trialsunmatched
- Problem Solving Skillsunmatched
- Regulatory Complianceunmatched
- Social Media Optimization (SMO)unmatched
- Spanish Languageunmatched
- Vision Planunmatched
- Willing to Travelunmatched
Description
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 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.
Bilingual in English/Spanish preferred
Requirements
- 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.
- Travel required to additional site locations in Hesperia and Barstow.
Must be local to Victorville, CA area – Full-time Onsite /this is not a remote or hybrid position
Benefits
- Medical, Dental, and Vision Insurance
- 401(k) with company match
- Paid Time Off (PTO)
Compensation: $23.00 - $32.00 per hour
About National Institute Of Clinical Research
NICR is a multi-site Site Management Organization (SMO) operating across California and Texas. With approximately 50 active trials across cardiovascular, cardiorenal, metabolic, neuropsychiatry, and infectious diseases, we are known for our strong enrollment performance and rapid operations. We are in an active growth phase and need a strategic leader to coordinate how we grow our sponsor relationships, investigator (PI) network, and overall market presence.
Who We Are
From our roots in Nephrology, we have expanded into many other specialty fields, including cardiometabolic, infectious diseases, geriatrics, and many other challenging & underserved areas of healthcare. We have dedicated ourselves to providing the highest quality clinical trials to our sponsors, investigators, and study volunteers.
We pride ourselves in our collective experience, industry knowledge, and dedication to moving patient health forward.
Numbers & Facts
| Location | Victorville, California |
| Website | https://www.nicresearch.com |
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