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$18

$44

$62

How much do clinical research iv jobs pay per hour?

As of Aug 15, 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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Clinical Research Iv jobs near you
Infographic showing various Clinical Research Iv job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $91,797 per year, or $44.1 per hour.

Clinical Research Coordinator

Headlands Research

Lake Worth, FL • On-site

$21.50 - $28.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
Clinical Research Coordinator (CRC)
Location: Lake Worth, FL | Site Name: JEM Research Institute | Full-Time
Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Lake Worth, FL. The CRC will manage and execute Phase II-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.
Type: Regular Full-time Employee
Schedule: Mondays through Fridays, 8:30am - 4:30pm
Location: Onsite in Lake Worth, FL (no capabilities for remote or hybrid work)
Reports to: Clinical Research Manager
Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.
What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • A mission-driven culture focused on advancing medicine and improving patient outcomes

Why Join Us?
You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.
Responsibilities:
  • Coordinate all aspects of assigned clinical trials from site initiation to study close-out
  • Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards
  • Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs
  • Manage subject recruitment, informed consent, and retention strategies
  • Ensure timely data entry and resolution of EDC queries
  • Report and follow up on all adverse events, serious adverse events, and deviations
  • Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems
  • Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control

Requirements:
  • Required: High school diploma or GED
  • Experience:
    • Minimum of 1 year of experience as a Clinical Research Coordinator OR
    • Minimum of 2 years of experience as a Research Assistant in Clinical Research
  • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
  • Proficiency in medical terminology and clinical documentation practices
  • Strong interpersonal, verbal, and written communication skills
  • Organized, detail-oriented, and capable of managing multiple priorities
  • Proficient in Microsoft Office and other clinical research systems
  • Bilingual (English/Spanish) is strongly preferred

Apply now to become a part of a team that's changing the future of healthcare-one trial at a time.
Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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