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Clinical Research Associate Cro Jobs in Nevada (NOW HIRING)

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred. * Basic knowledge of clinical research strongly preferred. * Medical terminology ...

Amgen

Imaging Specialist Manager

Las Vegas, NV · On-site +1

Experience at or oversight of outside clinical research vendors (CRO's, central labs, imaging vendors, etc.) * Experience in operationalizing global clinical studies with imaging and vendor ...

Danaher

Principal Clinical Scientist

Las Vegas, NV · On-site +1

Our associates are involved in every stage of diagnostics, from ideation to development and ... Partner crossfunctionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to ...

micro1 AI

Director of Biostatistics

Sparks, NV · Remote

$60 - $65/hr

... clinical research. In this role, you'll apply your expertise to help train next-generation AI ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Director of Biostatistics

Reno, NV · Remote

$60 - $65/hr

... clinical research. In this role, you'll apply your expertise to help train next-generation AI ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Henderson, NV · Remote

$60 - $65/hr

... clinical research. In this role, you'll apply your expertise to help train next-generation AI ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

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All JobsClinical Research Associate Cro JobsClinical Research Associate Cro Jobs in Nevada

Clinical Research Associate Cro information

What is the difference between Clinical Research Associate Cro vs Clinical Trial Assistant?

AspectClinical Research Associate CroClinical Trial Assistant
CredentialsBachelor's degree, often with certifications like CCRP or RACTypically a high school diploma or associate degree, with some roles requiring a certificate
Work EnvironmentConducts site visits, monitors trials, and ensures complianceSupports trial coordination, manages documentation, and assists with logistics
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, clinical trial teams

The Clinical Research Associate Cro focuses on monitoring clinical trials, ensuring compliance, and site management. In contrast, the Clinical Trial Assistant provides administrative support, manages documentation, and assists with trial logistics. Both roles are essential in clinical research but differ in responsibilities and required experience.

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Clinical Research Associate Cro jobs near you
Infographic showing various Clinical Research Associate Cro job openings in Nevada as of June 2026, with employment types broken down into 1% As Needed, 82% Full Time, 8% Part Time, 1% Temporary, and 8% Contract. Highlights an 72% Physical, 3% Hybrid, and 25% Remote job distribution.

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

Indero

Las Vegas, NV • On-site, Remote

Other

Re-posted 20 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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