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Contract Clinical Research Associate Jobs in Minnesota

Maple Grove, MN Duration: 8-month contract (likelihood of extension) Position Summary: Participates ... Certification as a Research Professional by Society of Clinical Research Associates (SoCRA) or ...

Position Summary The primary responsibility of the Clinical Research Associate I (CRA I) is support of the research team in the conduct of department research projects. Responsibilities include but ...

Position Summary The primary responsibility of the Clinical Research Associate I (CRA I) is support of the research team in the conduct of department research projects. Responsibilities include but ...

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Contract Clinical Research Associate information

See Minnesota salary details

$11

$40

$68

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

As of Aug 24, 2026, the average hourly pay for contract clinical research associate in Minnesota is $40.28, according to ZipRecruiter salary data. Most workers in this role earn between $28.27 and $51.54 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 Minnesota?

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

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

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

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

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

Infographic showing various Contract Clinical Research Associate job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 26% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $83,781 per year, or $40.3 per hour.

Sr Clinical Research Associate-Class III Device with Security Clearance

Minneapolis, MN โ€ข On-site

$110K/yr

Other

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Title: Senior Clinical Research Associate-Medical Device Pay: Starting at $110,000, DOE FT or PT: Full-time, Contract-to-hire (about 3 months to conversion) Location: Remote with domestic travel (25-50% anticipated) Kellyยฎ Science & Clinical is seeking a Senior Clinical Research Associate for a temp-to-hire position at an early-stage, innovation-driven medical device client. If you're passionate about supporting high-impact clinical studies and improving patient care in surgical settings, and are ready to take the next step in your career, trust The Experts at Hiring Experts. As a Senior Clinical Research Associate, you will be responsible for overseeing the execution of clinical trials from site start-up to site closure, ensuring compliance with study protocols, regulatory requirements, and maintaining quality documentation. Key responsibilities include coordinating and conducting site qualification, initiation, and monitoring visits; managing site operations; reviewing informed consent procedures; assessing investigational product accountability; and supporting the development of study documentation and site-facing presentation materials. You will develop strong relationships with clinical site staff, proactively identify and mitigate risks, and facilitate timely communication among stakeholders. Requirements: * Bachelor's Degree or higher in healthcare or science related field (alternately, relevant experience may be considered)
* Minimum 5 years' experience as a Clinical Research Associate
* At least 3 years of monitoring Class III medical device trials
* Proficiency with Epic required
* Thorough knowledge of clinical research concepts, FDA regulations, and Good Clinical Practice (GCP)
* Strong organizational, communication, and critical thinking skills
* Willingness and ability to travel domestically 25-50% of the time
* Experience in breast cancer, breast reconstruction, or related therapeutic areas preferred
* Proficient in Microsoft Office and comfortable learning new clinical trial management systems Our client offers a fast-paced, high-growth environment with opportunities for professional development and impactful work. If you have a passion for clinical research and medical devices, apply today! 10338188