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Clinical Research Associate Manager Jobs in Minnesota

Children's Minnesota

Position Summary The primary responsibility of the Clinical Research Associate I (CRA I) is support ... Manage personal career development and administrative tasks Baccalaureate degree or at least 4 ...

Children's Minnesota

Position Summary The primary responsibility of the Clinical Research Associate I (CRA I) is support ... Manage personal career development and administrative tasks Baccalaureate degree or at least 4 ...

Murphy Research

Research Associate

Minneapolis, MN · On-site

$50K - $52K/yr

We are actively seeking full-time Research Associates to join the Murphy Research consulting team ... You understand the importance of time management and the need to prioritize as you work on several ...

Murphy Research

Research Associate

Minneapolis, MN · On-site

$50K - $52K/yr

We are actively seeking full-time Research Associates to join the Murphy Research consulting team ... You understand the importance of time management and the need to prioritize as you work on several ...

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All JobsClinical Research Associate JobsClinical Research Associate Manager JobsClinical Research Associate Manager Jobs in Minnesota

Clinical Research Associate Manager information

See Minnesota salary details

$35.3K

$84.7K

$135.2K

How much do clinical research associate manager jobs pay per year?

As of Aug 24, 2026, the average yearly pay for clinical research associate manager in Minnesota is $84,675.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,900.00 and $111,700.00 per year, depending on experience, location, and employer.

What is a clinical research associate manager?

A Clinical Research Associate Manager is a professional responsible for overseeing and managing a team of Clinical Research Associates (CRAs) who monitor clinical trials to ensure they are conducted according to protocols, regulatory requirements, and good clinical practice. They coordinate trial activities, provide guidance and training to CRAs, and serve as a liaison between the research team, sponsors, and regulatory bodies. Their role is crucial for maintaining the quality and integrity of clinical research studies.

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

To thrive as a Clinical Research Associate Manager, you need expertise in clinical trial management, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and project management certifications like PMP are commonly required. Strong leadership, communication, and problem-solving skills help you effectively oversee teams and ensure adherence to protocols. These skills are crucial for ensuring high-quality research, regulatory compliance, and successful project delivery in clinical studies.

What are some common challenges faced by clinical research associate managers when overseeing multiple clinical trials simultaneously?

Clinical Research Associate Managers often face the challenge of balancing oversight across several ongoing clinical trials, each with unique protocols and site requirements. Managing competing deadlines, ensuring regulatory compliance, and maintaining clear communication across diverse teams are critical aspects of the role. Effective prioritization, strong organizational skills, and proactive risk management are essential to navigate these complexities and ensure trial success. Collaboration with CRAs, investigators, and cross-functional departments helps in addressing site issues promptly and maintaining study quality.

Is it hard to get a clinical research associate manager job?

Securing a clinical research associate manager position can be competitive, often requiring several years of experience in clinical research, strong leadership skills, and relevant certifications such as CCRP or RAC. Candidates with a background in clinical operations, good understanding of regulatory requirements, and proficiency with trial management tools tend to have better prospects.

What are popular job titles related to Clinical Research Associate Manager jobs in Minnesota?

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

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

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

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

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

Clinical Research Associate Manager jobs near you
Infographic showing various Clinical Research Associate Manager job openings in Minnesota as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, 2% Contract, and 1% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $84,675 per year, or $40.7 per hour.

Sr Clinical Research Associate-Class III Device with Security Clearance

Kelly FedSecur

Minneapolis, MN • On-site

$110K/yr

Other

This job post has expired today. 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) Kelly® 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

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