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Contract Clinical Research Associate Jobs in Nevada

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Contract Responsibilities * Assist in the coordination and execution of clinical research protocols ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Contract Responsibilities * Assist in the coordination and execution of clinical research protocols ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Contract Responsibilities * Assist in the coordination and execution of clinical research protocols ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Contract Responsibilities * Assist in the coordination and execution of clinical research protocols ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

Actalent

Clinical Research Coordinator

Las Vegas, NV

$25 - $33/hr

Clinical Research Coordinator This role is a part-time, on-site Clinical Research Coordinator ... Job Type & Location This is a Contract position based out of Las Vegas, NV. Pay and Benefits The ...

New

Actalent

Reno, NV- Clinical Research Coordinator

Reno, NV · On-site

$25 - $35/hr

Clinical Research Coordinator This part-time Clinical Research Coordinator role in Reno, NV offers ... Job Type & Location This is a Contract position based out of Reno, NV. Pay and Benefits The pay ...

Actalent

Clinical Laboratory Technician

Las Vegas, NV · On-site

$21/hr

Ability to adapt to changing study needs and perform additional duties as assigned in a fast-paced clinical research setting. Job Type & Location This is a Contract position based out of Las Vegas ...

Actalent

Clinical Laboratory Technician

Henderson, NV · On-site

$21/hr

Ability to adapt to changing study needs and perform additional duties as assigned in a fast-paced clinical research setting. Job Type & Location This is a Contract position based out of Las Vegas ...

Actalent

Clinical Laboratory Technician

Las Vegas, NV · On-site

$21/hr

Ability to adapt to changing study needs and perform additional duties as assigned in a fast-paced clinical research setting. Job Type & Location This is a Contract position based out of Las Vegas ...

IQVIA

CRA 1, IQVIA Biotech

Las Vegas, NV · On-site

$71K - $145K/yr

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.

IQVIA

CRA 1, IQVIA Biotech

Las Vegas, NV · On-site

$71K - $145K/yr

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.

IQVIA

CRA 1, IQVIA Biotech

Henderson, NV · On-site

$71K - $145K/yr

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.

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Contract Clinical Research Associate information

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

As of Aug 30, 2026, the average hourly pay for contract clinical research associate in Nevada is $41.88, according to ZipRecruiter salary data. Most workers in this role earn between $29.38 and $53.61 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.

What are popular job titles related to Contract Clinical Research Associate jobs in Nevada?

For Contract Clinical Research Associate jobs in Nevada, the most frequently searched job titles are:

What job categories do people searching Contract Clinical Research Associate jobs in Nevada look for?

The top searched job categories for Contract Clinical Research Associate jobs in Nevada are:

What cities in Nevada are hiring for Contract Clinical Research Associate jobs?

Cities in Nevada with the most Contract Clinical Research Associate job openings:

Contract Clinical Research Associate jobs near you
Infographic showing various Contract Clinical Research Associate job openings in Nevada as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $87,108 per year, or $41.9 per hour.

Senior Clinical Research Associate, Dermatology & Rheumatology, US West Region (NV,KS,AZ)

Las Vegas, NV • On-site, Remote

Indero
See more jobs at Inderoexternal

Other

Re-posted 13 days ago

Job description

Description
Senior Clinical Research Associate - Dermatology & Rheumatology | US West Region (Nevada, Kansas and/or Arizona preferred)
The senior clinical research associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
This role will be perfect for you if:
  • You are a seasoned Clinical Research Associate (CRA) who thrives in autonomous environments and consistently meets high-quality standards and deadlines.
  • You bring experience in dermatology and rheumatology, and you're eager to deepen your expertise in these therapeutic areas.
  • You value working within a mid-sized CRO where your contributions are visible, appreciated, and have a direct impact.

RESPONSIBILITIES
The senior clinical research associate (CRA):
  • Conducts site qualification, initiation, monitoring, and close-out visits for research sites according to the monitoring plan, Innovaderm and sponsor SOPs, ICH/CGP guidelines and applicable regulations
  • Participates in investigators' meetings
  • Prepares site visit reports and follow-up letters to the investigator
  • Builds productive relationships with investigators and site staff to achieve study objectives, including patient recruitment targets
  • Performs source data verification, ensures on-site study drug storage, dispensing, and accountability, data collection, and regulatory document collection is adequate

The Sr CRA may also assume the following Lead CRA responsibilities:
  • Reviews and approves site visit reports.
  • Tracks site visit and trip report metrics and escalates issues to project teams.
  • Recommends potential solutions to identified issues and work with the project managers to find resolution.
  • Supports the development of annotated site visit reports, clinical monitoring plans, and monitoring tools.
  • Supports the preparation and development of materials related to the training of CRAs.
  • Mentors CRAs.
  • Conducts on-site quality control visits with CRAs.

Requirements
Education
  • B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience

Experience
  • At least 5 years experience in conducting on-site clinical monitoring in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry
  • Rheumatology exposure

Knowledge and skills
  • Good knowledge of ICH/GCP standards and applicable regulatory requirements
  • Strong verbal and written communication skills in English
  • Ability to prioritize different assignments and work under pressure while maintaining attention to detail and meeting timelines
  • Excellent judgement and problem-solving skills
  • Travel to research sites approximately 65% of the time
  • Excellent knowledge of Microsoft Office (i.e., Word, Excel, PowerPoint)
  • Experience in dermatology

Our company
The work environment
At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.
Recruitment process: what to expect
  • As part of the recruitment process for this position you will meet various team members at Indero
  • The first interview will be conducted by Teams (30 minutes) and the second via video conference (1 hour)

About Indero
A Global Clinical Leader In Dermatology and Rheumatology!
Formerly known as Innovaderm, Indero is a world-renowned expert and clinical research leader in dermatology. We have more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint.
Indero is a dual-focus CRO for dermatology and rheumatology, with 25+ years' experience in clinical research and trial delivery. Our full-service approach - which includes everything from protocol design and patient recruitment to trial monitoring and biometrics - provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively. With capabilities in North America, Europe, Asia Pacific and Latin America; vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies, Indero is the ideal CRO partner for clinical needs at global scale.
Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.
Indero only accepts applicants who can legally work in the US regions.

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