Top 86 Clinical research associate Jobs in Maple Grove Mn

Clinical Research Associate (CRA) III
CVRx, Inc. —Brooklyn Park, MN
- $127,000 - $142,000 a year
- Full-time
- Ability to walk for extended periods
- Mid-level
- Bachelor's degree
- Health savings account
- Employee stock purchase plan
Quick Apply
Clinical Research Associate II
Inspire Medical Systems Inc. —Minneapolis, MN
- $95,000 - $125,000 a year
- Patient monitoring
- Bachelor of Science
- Mid-level
- Health savings account
- Employee stock purchase plan
Quick Apply
Clinical Research Associate II
Inspire Medical Systems —Minneapolis, MN
- $95,000 - $125,000 a year
- Patient monitoring
- Bachelor of Science
- Mid-level
- Health savings account
- Employee stock purchase plan
Clinical Research Coordinator
University of Minnesota —Minneapolis, MN
- Online Application
- Background check
- Bachelor of Science
- HIPAA
14d
Senior Clinical Research Associate
AtriCure —Minnetonka, MN
- $106,000 - $130,000 a year
- Remote
- 5 years
- Bachelor's degree
- Travel
- Paid parental leave
- Health insurance
Safety Clinical Research Associate (on-site)
Abbott Laboratories —Maple Grove, MN
- $61,300 - $122,700 a year
- Full-time
- Nursing
- Mid-level
- Bachelor's degree
- Continuing education credits
- Health insurance
9d
PSG Tech and Clinical Research Coordinator
University of Minnesota —Minneapolis, MN
- Online Application
- Background check
- Patient monitoring
- Bachelor of Science
11d
Clinical Research Coordinator (Research Professional 2)
University of Minnesota —Minneapolis, MN
- Part-time
- Background check
- Psychiatry
- Hospital
Clinical Research Coordinator, RP3
University of Minnesota —Minneapolis, MN
- Online Application
- Background check
- Bachelor of Science
- HIPAA
9d
Research Professional 1-Clinical Research
University of Minnesota —Minneapolis, MN
- Part-time
- Background check
- Bachelor of Science
- Mid-level
- Work from home
4d
Clinical Research Nurse 2
University of Minnesota —Minneapolis, MN
- Online Application
- Background check
- Nursing
- RN License
14d
Clinical Research Professional – Neurostimulation Research in Mental Illness - (Research Professional 1)
University of Minnesota —Minneapolis, MN
- Online Application
- Background check
- Psychiatry
- Hospital
9d
Clinical Trials Research Assistant
Retina Minnesota MSO LLC —Edina, MN
- $22 - $28 an hour
- Full-time
- Patient monitoring
- Laboratory experience
- High school diploma or GED
- Health savings account
- Paid holidays
Clinical Research Coordinator
CENTER FOR VETERANS RESEARCH AND EDUCATION —Minneapolis, MN
- $48,000 - $75,000 a year
- Weekends as needed
- Background check
- Microsoft Excel
- Microsoft Outlook
Quick Apply
Clinical Research Coordinator
Fairview Health Services —Saint Paul, MN
- $29.29 - $41.35 an hour
- Weekends as needed
- Bachelor of Science
- Inpatient
- Mid-level
Clinical Research Coordinator
MNGI Digestive Health —Minneapolis, MN
- $60,153.60 - $69,180.80 a year
- Full-time
- Hybrid work
- Writing skills
- Mid-level
- Clinic
- Profit sharing
- Paid holidays
Quick Apply
Clinical Research Coordinator 1
University of Minnesota —Minneapolis, MN
- Online Application
- Background check
- Computer literacy
- Bachelor of Science
2d
Research Assistant
University of Minnesota —Minneapolis, MN
- Part-time
- Background check
- Classroom
- Spanish
Research Assistant
Fairview Health Services —Saint Paul, MN
- $21.84 - $30.83 an hour
- Full-time
- Computer Science
- Mid-level
- Quality control
Research Assistant - Research Professional 2
University of Minnesota —Minneapolis, MN
- 8 hour shift
- Background check
- Vital signs
- Medication administration

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Clinical Research Associate (CRA) III

CVRx, Inc.
Brooklyn Park, MN

Quick Apply

Job Details

Full-time
$127,000 - $142,000 a year

Benefits

Stock options
Health savings account
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
RSU
Paid time off
401(k) matching
Flexible schedule
Life insurance

Qualifications

Professional ethics
Bachelor's degree
Clinical quality assurance standards
Cross-functional collaboration
Medical terminology
Cross-functional communication

Full Job Description

Why work for CVRx?

CVRx pioneers' unique therapies that harness and harmonize the body’s natural systems, benefiting society and making CVRx a universal role model in healthcare. We value our commitments to others and continue to overcome challenges through determination, collaboration and purpose. If our culture and values speak to you, and if you have a passion for cutting-edge medical technologies, join our team and our mission to help others live better lives.

This position is remote. Our ideal candidate will reside near our headquarters in Brooklyn Park, MN for occasional on-site visits.

The Role

The Clinical Research Associate III (CRA III) will be responsible for the day-to-day operations associated with the execution of clinical trials and monitoring the clinical trial sites to ensure they are complying to the applicable study protocol, Standard Operating Procedures (SOPs), CVRx requirements, Good Clinical Practice (GCP), and the applicable regulatory requirement(s). The CRA III will work closely with the Clinical Study Manager to ensure site day-to-day operations and monitoring is executed to meet project deliverables. CRA III is expected to work from the CVRx office, or at the sites when monitoring.

KEY DUTIES AND RESPONSIBILITIES

Develops and maintains successful working relationships with study sites and serves as the primary point of contact.

Assists in preparation of study materials and training of investigators and site staff

Supports Clinical Centers in the execution of site IRB or ethics committee submissions

Responsible for the collection and tracking of required regulatory documents from Clinical Centers

Coordinates and conducts monitoring (as directed by the monitoring plan) at participating centers to ensure compliance with the protocol and applicable regulations, as well as the timely receipt of accurate data and other required study documents

Prepares and submits high-quality monitoring reports per study-specific requirements

Evaluate site performance through analysis of enrollment trends, data quality metrics, protocol deviations, product accountability, and patient safety parameters

Support sites in AE/SAE identification, documentation, and reporting

Verify timely submission of required safety documentation, device complaint forms, and follow-up queries

Drive proactive risk identification at the site level and support the execution of risk-mitigation plans

Source verifies clinical data/information and oversees data correction to match source

Maintains Clinical Study files

Manages device accountability at site (if applicable)

Processes payments to sites, vendors, and consultants

Reviews clinical data/information and oversees data correction

Reviews center activation documentation

Work closely with Clinical Project Managers, Data Management, Safety, Regulatory, Quality, and Training to ensure end-to-end study execution

Provide operational input on protocol development, CRFs, risk assessments (RACT), monitoring plans, investigational brochures, and essential document requirements

Collaborate in Trial Master File (TMF) quality checks to ensure site-level documentation is complete, audit-ready, and compliant

Contribute to process improvement initiatives, QMS updates, and clinical operations optimization

Assist management in metrics reporting, monitoring dashboards, and early risk detection through data analytics

Participate in vendor oversight (central labs, imaging, core labs) to ensure site compliance (if applicable)

Assists in training new Clinical Research Associates

Assists with successful conduct of assigned studies. This includes interfacing with representatives from key functional groups including Regulatory Affairs and Quality Assurance, Research & Development, U.S. Market Development, Commercial Development and Clinical Research Organizations

Provides mentoring regarding site monitoring to internal team

Completes special projects and performs job-related duties as assigned

REQUIRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE

Bachelor’s degree

5+ years experience directly supporting clinical research or similar experience in a medical/scientific area

2+ years experience in monitoring clinical trial sites

Knowledge of GCP’s and regulatory compliance guidelines for clinical trials

Knowledge of medical terminology

High attention to detail and accuracy

Able to manage multiple tasks and operate independently

Operates in an efficient and expedient manner

High ethical standards and integrity

Strong team player with experience working cross-functionally and maintaining high-performance standards

Comfortable in a small company and thrives in a high-growth environment

Advanced written and oral communications skills

Good problem-solving skills

Adaptable, resourceful, and comfortable navigating change

Entrepreneurial approach

PREFERRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE

Advanced degree in a related field is preferred

WORKING CONDITIONS AND REQUIRED PHYSICAL EFFORT

Normal office conditions and a reliable internet connection when working in a home office
Must be able to sit/stand/walk 8 hours per day
Position requires up to 40% travel
May be required to be fully vaccinated against the COVID-19 virus and other diseases

CVRx is unable to provide employment visa sponsorship for this position. Candidates must be legally authorized to work in the United States without current or future sponsorship

What we offer:

CVRx is proud to offer competitive salaries and benefits plans.

We offer a culture of teamwork, collaboration, and positivity, where challenging the status quo is welcomed, continuous learning is valued, and each of us has an opportunity to make a significant impact in an exciting, purpose-driven startup environment while also having fun.

Salary range for U.S locations (USD): 127,000 - 142,000 per year.

The pay range is applicable across the U.S., complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and specific location.

We also offer a competitive and rewarding benefits package, details listed below:

Competitive Health & Dental Insurance options with generous Company contributions
Company contributions to an HSA with a high deductible insurance plan selection
401(k) with a company match
Employee stock purchase plan (ESPP) & stock option and RSU grants
12 company-paid holidays per year in addition to a generous Flex PTO plan
Generous paid time off for new parents
Company-paid life insurance & disability options
Unlimited growth opportunities in a growing company
Endless training & learning opportunities
Flexible Schedule

EEO STATEMENT

CVRx, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

If you're an independent, self-motivated individual with excellent interpersonal skills, a desire to do great things and have a background in medical devices, healthcare or a related field, we want to hear from you!

If you need assistance or an accommodation due to a disability, you may contact us at [email protected]

CVRx Privacy Policy
CVRx SMS Terms of Service

This requisition will be open until filled.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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Refine Your Search

clinical research associate jobs in maple grove mn

Clinical Research Associate (CRA) III

Clinical Research Associate II

Clinical Research Associate II

Clinical Research Coordinator

Senior Clinical Research Associate

Safety Clinical Research Associate (on-site)

PSG Tech and Clinical Research Coordinator

Clinical Research Coordinator (Research Professional 2)

Clinical Research Coordinator, RP3

Research Professional 1-Clinical Research

Clinical Research Nurse 2

Clinical Research Professional – Neurostimulation Research in Mental Illness - (Research Professional 1)

Clinical Trials Research Assistant

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator 1

Research Assistant

Research Assistant

Research Assistant - Research Professional 2

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KEY DUTIES AND RESPONSIBILITIES

REQUIRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE

PREFERRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE

WORKING CONDITIONS AND REQUIRED PHYSICAL EFFORT

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