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Orison Solutions

CRA- Analyst

Minneapolis, MN · On-site

$30 - $32/hr

Monitor Clinical Research Organizations (CROs) and study management of multiple sites. * Additional ... In-house pharma CRA experience (strictly Regional CRA experience will be considered) * Clinical ...

Orison

CRA- Analyst

Minneapolis, MN · On-site

Monitor Clinical Research Organizations (CROs) and study management of multiple sites. * Additional ... In-house pharma CRA experience (strictly Regional CRA experience will be considered) * Clinical ...

IQVIA

CRA 2/Senior CRA

Dallas, TX

$90K - $175K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

IQVIA

CRA 2/Senior CRA

Sacramento, CA

$90K - $175K/yr

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

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How much do cra research jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for cra research 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.

How hard is it to get a CRA job?

Securing a CRA (Clinical Research Associate) position typically requires a relevant degree in life sciences or healthcare, along with experience in clinical trials or regulatory environments. Employers often look for strong organizational skills, knowledge of Good Clinical Practice (GCP), and proficiency with trial management tools, making entry competitive but achievable with proper qualifications and certifications.

What is the difference between Cra Research vs Clinical Research Coordinator?

AspectCra ResearchClinical Research Coordinator
Required CredentialsBachelor's degree, often with certifications like CCRP or CRA certificationBachelor's degree, often with certifications like CCRP or CRC certification
Work EnvironmentPharmaceutical companies, Contract Research Organizations (CROs), biotech firmsHospitals, clinics, research sites, academic institutions
Employer & Industry UsageUsed mainly in pharmaceutical and biotech industries for drug developmentCommon in healthcare settings for managing clinical trials

Cra Research and Clinical Research Coordinator roles share similar credentials and work environments but differ mainly in their focus. Cra Research typically involves overseeing clinical trial data and regulatory compliance in pharma or biotech companies, while Clinical Research Coordinators manage day-to-day trial activities at research sites. Both roles are essential in clinical research but serve different functions within the industry.

What are some typical challenges a CRA (Clinical Research Associate) might face when monitoring clinical trial sites, and how can these be managed?

CRAs often encounter challenges such as ensuring site compliance with study protocols, managing tight timelines, and maintaining clear communication with site staff. Addressing these requires strong organizational skills, attention to detail, and the ability to build collaborative relationships with site teams. Proactive planning, regular site visits, and effective use of monitoring tools help CRAs manage these challenges and ensure trials run smoothly.

What jobs pay $10,000 a month without a degree?

For a CRA researcher, high-paying roles without a degree are uncommon, as clinical research associate positions typically require relevant certifications or experience. However, some sales, real estate, or tech roles such as software sales or digital marketing can reach or exceed $10,000 monthly with strong skills and performance. These jobs often rely on commissions, experience, and self-education rather than formal degrees.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (CRA), and why are they important?

To thrive as a Clinical Research Associate (CRA), you need a solid background in life sciences, clinical research processes, and regulatory guidelines, usually supported by a relevant degree and industry certifications such as ACRP or SOCRA. Familiarity with electronic data capture (EDC) systems, trial management software, and Good Clinical Practice (GCP) standards is typically required. Attention to detail, strong organizational skills, and effective communication are essential soft skills for managing study sites and interacting with diverse teams. These competencies ensure regulatory compliance, data integrity, and the smooth execution of clinical trials.

What jobs pay $500,000 a year in the US?

In the field of CRA research, high-paying roles such as senior clinical research directors or chief scientific officers can reach or exceed $500,000 annually, especially in large pharmaceutical or biotech companies. These positions typically require extensive experience, advanced degrees, and leadership skills, often involving strategic oversight and regulatory knowledge.

What is the role of a CRA in research?

A Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They oversee site activities, verify data accuracy, and communicate with investigators, often using electronic data capture systems, to support the integrity and quality of the research process.

What are CRA (Clinical Research Associate) research jobs?

CRA research jobs involve overseeing and monitoring clinical trials to ensure they comply with regulatory requirements and study protocols. Clinical Research Associates (CRAs) are responsible for visiting clinical sites, ensuring data accuracy, verifying patient safety, and maintaining proper documentation. They act as a bridge between the study sponsor and the clinical trial site, helping to ensure trials are conducted ethically and effectively. CRAs often travel to different locations and must have a strong understanding of clinical research regulations and Good Clinical Practice (GCP) guidelines.
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Cra Research jobs near you

Clinical Research Associate/Monitor

Futran Tech Solutions Pvt. Ltd.

Remote

Contractor

Posted yesterday

Job description

Job Title: Clinical Research Associate/Monitor
6 months contract to perm
Work location: REMOTE
Required 30%-50% traveling
Candidate home location: required within DC, VA, MD only (a candidate needs to reside in DC, VA, MD)
Multiple Regional CRAs: 5 openings
USC/GC required
Search Term: Regional CRA, Contract CRA, Sr. CRA, Home-based CRA, Regional Clinical Research Associate, Regional CRA III, Sr. Clinical Research Associate, Senior Clinical Research Associate, Monitor, Contract CRA II, CRA III, Regional Monitor, Home-based Regional CRA, CRA, Contract Clinical Research Associate, Regional CRA Consultant, Phase I, Study Monitor, Contract Monitor, CRA, Research Associate
Multiple Studies with Health patients - Previous Phase I experience required
Contract CRAs, regional based with strong monitoring skills, minimum 3-5+ years monitoring experience within the pharmaceutical industry required traveling of minimum of 50% traveling to 1-2 sites within the same state as required. Require 100% commitment and contractors paid hourly. Therapeutic areas can range and candidates will be expected on working on about 6-8 protocols (max at 10 protocols) with different indications. Multiple sites and candidate has to be local to DC, VA, and MD areas.
Minimum 3-5+ years of CRA / Monitoring experience required
Start date is ASAP
TRAVEL INFORMATION FOR CANDIDATES -
The client is working to ensure candidates are as close as possible to their sites. Company is constantly adding new studies to the monitoring project. Monitors may be asked to take on additional sites closer to their home (or maybe a bit further then what they currently have) - they will work to keep travel as regionally located as possible. There are multiple sites in each region (depends on the allocation of the individual CRAs)
In addition they should be very clear about their monitoring experience showing that they are a Regional CRA/monitor currently. (I would say 3 years monitoring experience with Oncology study required) Candidates need to allocate 50% to 100% of their time to this assignment, preferred candidates home is close to the site locations (listed above).The CRA/Study Monitor designated activities include site visits, trial monitoring, tracking, documentation, collection, solicitation and review of (e) CRFs and submit data, preparation of reports, regulatory review and participation in teleconferences. Approximately 50% travel will be required, as the CRA Study Monitor's primary responsibilities will be monitoring of study sites.
Requirements
A strong healthcare background with at least 1-2 years prior monitoring Oncology study experience is required. Phase I research experience as a monitor, auditor, research coordinator, research associate or similar oncology research experience is required. The CRA/Study Monitor must hold a Bachelor's degree from an accredited college or University or be a grad from an accredited school of nursing.
Requirement:
  • 2+ years prior monitoring Oncology study experience is required. preferred. Phase I-IV research experience as a monitor, clinical research associate experience is required.
  • BS/BA in life sciences or health-related discipline, BSN, Bachelor of Science - Nursing, Pharmacy is highly desirable.
  • Minimum 3-5+ years clinical research monitoring experience including years in Phase I studies.
  • Strong working knowledge of GCPs, ICH Guidelines, and FDA Regulations
  • Ability and willingness to travel up to 50 % of the time, including minimum overnight stays travel as necessary
  • Experience with regulatory document review/collection and IRB submissions (including OHRP regulations), a plus
  • Experience with using a Trial Master File, a plus.

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