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Contract Clinical Research Associate Jobs (NOW HIRING)

ScholarshipsAds Inc.

Redwood City, CA Length: 6 Month Contract Were seeking a Clinical Research Associate (CRA) with strong clinical monitoring experience to support a growing clinical team. This is a monitoring-focused ...

North American Science Associates, Inc.

$100K/yr

Assists with the coordination of the site budget and contract negotiations as directed by the ... Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical ...

Adecco

Clinical Research Associate

Waltham, MA · On-site

$32 - $33.75/hr

Temporary / Contract Schedule: Full-Time | Onsite Pay Rate: $32.00-$33.75 per hour Job Summary We are seeking a detail-oriented and motivated Clinical Research Associate to support clinical research ...

ClinChoice

Senior Clinical Research Associate

May assist with contract negotiation with sites on study budget after appropriate training ... Guide and supervise Clinical Research Associate I (CRA I) to coach and train them on the job.

ClinChoice

Senior Clinical Research Associate

May assist with contract negotiation with sites on study budget after appropriate training ... Guide and supervise Clinical Research Associate I (CRA I) to coach and train them on the job.

NAMSA

Senior Clinical Research Associate

$100K/yr

Assists with the coordination of the site budget and contract negotiations as directed by the ... Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical ...

UNAVAILABLE

TI Clinical Research Associate

Portland, OR · On-site

This TI Clinical Research Associate will be known internally as a Float Clinical Research Associate (Float CRA). It is a collaborative role supporting clinical research programs of the Knight Cancer ...

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How much do contract clinical research associate jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for contract clinical research associate in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is a contract clinical research associate?

Contract Clinical Research Associates (CRAs) are professionals who monitor clinical trials on behalf of pharmaceutical companies, contract research organizations (CROs), or other sponsors, but work on a contract or freelance basis rather than as permanent employees. Their primary responsibilities include ensuring that trials are conducted according to regulatory guidelines, monitoring data accuracy, and verifying that patient rights and safety are protected. Contract CRAs may work on multiple projects for different clients and often enjoy more flexibility in their schedules and work locations. This role requires strong organizational skills, knowledge of Good Clinical Practice (GCP), and the ability to travel to clinical sites.

What are some of the unique challenges faced by contract clinical research associates compared to permanent employees?

Contract Clinical Research Associates often need to quickly adapt to new study protocols, sponsor requirements, and team dynamics since they may work on multiple projects for different organizations. This can mean a faster onboarding process and the need to build rapport with new colleagues and site staff efficiently. Additionally, contract CRAs must be highly organized to manage shifting assignments and maintain compliance across different trial sites, as well as keep up with varying documentation standards. While this variety can be rewarding, it can also present challenges in terms of consistency and long-term project ownership.

What are the key skills and qualifications needed to thrive as a contract clinical research associate, and why are they important?

To thrive as a Contract Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP and ICH), and typically a degree in life sciences or related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly valued. Strong attention to detail, organizational skills, and effective communication help build productive site relationships and ensure compliance. These skills are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting successful clinical trial outcomes.

What is the difference between Contract Clinical Research Associate vs Clinical Research Associate?

AspectContract Clinical Research AssociateClinical Research Associate
CredentialsTypically requires a degree in life sciences and relevant certificationsSame as Contract CRA, often with additional experience
Work EnvironmentTemporary, project-based assignments often with multiple sponsorsFull-time employment with a single organization or sponsor
Employer & Industry UsageUsed by CROs and pharma companies for short-term projectsCommonly employed directly by pharmaceutical companies or CROs
Search & Comparison IntentOften compared for flexibility and contract work benefitsViewed as a permanent role with career growth

In summary, Contract Clinical Research Associates work on temporary, project-specific basis, often with multiple sponsors, offering flexibility. Clinical Research Associates typically hold full-time roles within a single organization, providing stability and career development opportunities.

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Contract Clinical Research Associate jobs near you
Infographic showing various Contract Clinical Research Associate job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Contract Clinical Research Assistant

Las Vegas, NV

Kelly Services
See more jobs at Kelly Servicesexternal

$28 - $30/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

New

Job description

Clinical Research Coordinator
Location: Las Vegas, NV
Schedule: Monday–Friday | Business Hours | 
Pay Rate: $28.00 – $30.00/hour
Job Type: Full-Time | Now until 1/2027. This opportunity could be extended past the end of the year and  has the potential for a CRC to convert to a permanent employee based on the site needs 
At Kelly Science & Clinical, we connect talented professionals with industry-leading organizations advancing healthcare and scientific innovation. This contract opportunity offers the chance to gain valuable clinical research experience while working alongside a collaborative and dedicated research team. We are currently accepting applications for a contract Clinical Research Coordinator to support one of our leading clinical research site network clients in Las Vegas Nevada. If you have experience supporting clinical trials, enjoy working directly with patients, and thrive in a fast-paced research environment, please apply today. 
Position Summary
The Clinical Research Coordinator (CRC) supports the day-to-day coordination and execution of clinical research studies while ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. This role partners closely with investigators, research staff, and study participants to ensure high-quality clinical research and an exceptional participant experience.
Responsibilities
  • Coordinate and support clinical research studies in accordance with study protocols and regulatory requirements.
  • Screen potential study participants and collect medical histories and other required information.
  • Assist with the informed consent process and participant enrollment.
  • Schedule study visits, procedures, and participant follow-up activities.
  • Collect, document, and maintain accurate source documentation and clinical research data.
  • Educate participants on study requirements and respond to study-related questions.
  • Monitor study progress and report adverse events, protocol deviations, and other research-related findings.
  • Maintain study files and documentation through scanning, uploading, filing, and record management.
  • Draw, process, package, and ship laboratory specimens when qualified.
  • Follow site SOPs, HIPAA, GCP, FDA regulations, and other applicable research standards.
  • Support additional research activities as assigned.
Qualifications
  • High school diploma or equivalent required; Associate's degree or higher in a health-related field preferred.
  • Previous clinical research experience or foundational knowledge of clinical research strongly preferred.
  • Experience with patient care and medical terminology required.
  • Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
  • Excellent communication and interpersonal skills.
  • Proficiency with Microsoft Office and electronic data capture (EDC) systems preferred.
  • Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines preferred.
  • Experience with participant screening and informed consent is highly desirable.
Preferred Certifications
  • Medical Assistant (MA) certification preferred.
  • Current CPR/BLS certification preferred.
  • Certified Clinical Research Coordinator (CCRC) certification, or willingness to obtain certification, preferred.

 
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
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