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Clinical Research Iv Jobs (NOW HIRING)

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$32.17/hr

The Clinical Research Coordinator IV assists with screening of potential patients, preparation and maintenance of research records, data collection, specimen processing and scheduling of research ...

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$18

$44

$62

How much do clinical research iv jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for clinical research iv in the United States is $44.13, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $52.40 per hour, depending on experience, location, and employer.

What is the difference between Clinical Research IV vs Clinical Research Coordinator?

AspectClinical Research IVClinical Research Coordinator
Required CredentialsBachelor's degree, often with clinical or scientific background; certifications like CCRPHigh school diploma or equivalent; often some college or certification in clinical research
Work EnvironmentPharmaceutical companies, CROs, or research institutions; often in clinical trial sitesResearch sites, hospitals, clinics; direct interaction with patients and study teams
Employer & Industry UsageUsed in clinical trial management, often with more responsibilitiesUsed in patient recruitment, data collection, and study coordination

Clinical Research IV professionals typically have more advanced education and handle higher-level responsibilities in managing clinical trials, while Clinical Research Coordinators focus on day-to-day trial operations and patient interactions. Both roles are essential in the clinical research process but differ in scope and experience requirements.

What are the key skills and qualifications needed to thrive as a Clinical Research IV, and why are they important?

To thrive as a Clinical Research IV, you need advanced knowledge of clinical trial design, regulatory compliance, and data management, typically supported by a relevant degree and significant experience in clinical research. Expertise in clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as SOCRA or ACRP are often required. Strong leadership, analytical thinking, and effective communication distinguish top performers in this role. These skills ensure rigorous study conduct, regulatory adherence, and successful collaboration across multidisciplinary research teams.

What is a Clinical Research IV?

A Clinical Research IV is an advanced-level clinical research professional who manages and oversees complex clinical trials and research projects. They are typically responsible for coordinating all aspects of the study, ensuring compliance with regulatory requirements, mentoring junior staff, and serving as a liaison between investigators, sponsors, and regulatory agencies. Clinical Research IVs often have several years of experience and may contribute to protocol development, data analysis, and publication of research findings. Their role is crucial in ensuring the integrity and success of clinical studies.

What are some typical challenges faced by Clinical Research IV professionals, and how can they be addressed?

Clinical Research IV professionals often encounter challenges such as managing complex, multi-site trials, ensuring regulatory compliance, and coordinating large, interdisciplinary teams. To address these, strong organizational skills, clear communication, and a proactive approach to problem-solving are essential. Leveraging project management tools and maintaining up-to-date knowledge of industry regulations can also help streamline processes and ensure successful study outcomes.
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What job categories do people searching Clinical Research Iv jobs look for? The top searched job categories for Clinical Research Iv jobs are:
Clinical Research Iv jobs near you
Clinical Research Coordinator

Clinical Research Coordinator

National Institute of Clinical Research, Inc.

Victorville, CA • On-site

$23 - $32/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 22 days ago

Job 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 is a plus!

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.
Must be local to Victorville, CA area – this is not a remote position.

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