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Contract Clinical Research Jobs (NOW HIRING)

Contract Compensation: $26.00-$30.00/hr Work Model: 100% Onsite Hours: 40.0 We are seeking a dedicated Clinical Research Coordinator to join our team in Inglewood, California. In this role, you will ...

Contract Compensation: $26.00-$30.00/hr Work Model: 100% Onsite Hours: 40.0 We are seeking a dedicated Clinical Research Coordinator to join our team in Inglewood, California. In this role, you will ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Showing results 21-40

Contract Clinical Research information

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$49K

$107.3K

$189K

How much do contract clinical research jobs pay per year?

As of Aug 16, 2026, the average yearly pay for contract clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a contract clinical research?

A Contract Clinical Research job involves working on a temporary or project-based basis to support clinical trials and research studies. Professionals in this role ensure compliance with regulatory standards, oversee study protocols, and manage data collection and reporting. They often work for pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. These roles require expertise in clinical trial processes, good clinical practices (GCP), and regulatory guidelines. Contract positions vary in duration and may offer flexibility in location and work arrangements.

What are the key skills and qualifications needed to thrive in the contract clinical research position, and why are they important?

To thrive in Contract Clinical Research, you need a strong background in clinical trial processes, regulatory compliance (such as GCP/ICH guidelines), and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like CCRA or CCRC are often required. Excellent organizational, communication, and problem-solving skills are vital for managing multiple projects and collaborating with cross-functional teams. These abilities ensure the smooth and ethical conduct of clinical trials while meeting tight timelines and quality standards.

What are the typical day-to-day responsibilities for someone in a contract clinical research role?

In a Contract Clinical Research position, you will typically oversee the execution of clinical trials, which includes tasks such as monitoring study sites, ensuring regulatory and protocol compliance, and managing study documentation. You'll collaborate closely with principal investigators, sponsors, and clinical site staff to ensure timelines are met and data is collected accurately. Responsibilities may also include preparing reports, assisting with site selection or initiation, and resolving any study-related issues that arise. This dynamic role often requires balancing administrative, technical, and interpersonal tasks to successfully support clinical research projects.

More about Contract Clinical Research jobs

What cities are hiring for Contract Clinical Research jobs?

Cities with the most Contract Clinical Research job openings:

What are the most commonly searched types of Clinical Research jobs?

The most popular types of Clinical Research jobs are:

What states have the most Contract Clinical Research jobs?

States with the most job openings for Contract Clinical Research jobs include:

Infographic showing various Contract Clinical Research 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 $107,336 per year, or $51.6 per hour.

Clinical Research Coordinator

System One

Inglewood, CA • On-site

$26 - $30/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago


Job description

Job Title: Clinical Research Coordinator Location: Inglewood, California Type: Contract Compensation: $26.00-$30.00/hr Work Model: 100% Onsite Hours: 40.0 We are seeking a dedicated Clinical Research Coordinator to join our team in Inglewood, California. In this role, you will assist with the coordination and execution of clinical research studies, ensuring compliance with all regulatory guidelines. This position involves screening participants, managing study documentation, and supporting study procedures to ensure smooth operations. This is an onsite, contract opportunity offering engaging work in a dynamic research environment.

Responsibilities

  • Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff.
  • Conduct screening visits to collect medical history & other information from study participants.
  • Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines.
  • Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams.
  • Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards.
  • Communicate with study participants to provide education, answer questions, and support adherence to study requirements.
  • Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team.

Requirements

  • High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred.
  • Experience with participant screening and the informed consent process strongly preferred.
  • Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred.
  • Current CPR/BLS certification preferred.
  • Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#LI-EL-1 Ref: #568-Clinical