The Clinical Study Manager must be able to work independently on multiple complex clinical studies using critical thinking skills. This position may be part of a small, cross functional team or may ...
New
The Clinical Study Manager must be able to work independently on multiple complex clinical studies using critical thinking skills. This position may be part of a small, cross functional team or may ...
New
Clinical Study Manager
Fridley, MN · On-site
$110K - $160K/yr
About the role The Clinical Study Manager is a key member of the Clinical Affairs team, responsible for leading the operational execution and management of clinical studies that support the company ...
Clinical Study Manager
Fridley, MN · On-site
$110K - $160K/yr
About the role The Clinical Study Manager is a key member of the Clinical Affairs team, responsible for leading the operational execution and management of clinical studies that support the company ...
Senior Clinical Study Manager
$106K - $145K/yr
The Clinical Study Manager must be able to work independently on multiple complex clinical studies using critical thinking skills. This position may be part of a small, cross functional team or may ...
New
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Senior Clinical Study Manager
$106K - $145K/yr
The Clinical Study Manager must be able to work independently on multiple complex clinical studies using critical thinking skills. This position may be part of a small, cross functional team or may ...
New
Senior Clinical Study Manager
Minneapolis, MN · On-site
$106K - $145K/yr
The Clinical Study Manager must be able to work independently on multiple complex clinical studies using critical thinking skills. This position may be part of a small, cross functional team or may ...
New
Senior Clinical Study Manager
Minneapolis, MN · On-site
$106K - $145K/yr
The Clinical Study Manager must be able to work independently on multiple complex clinical studies using critical thinking skills. This position may be part of a small, cross functional team or may ...
New
Senior Clinical Study Manager
Chaska, MN · On-site
$135K/yr
The Senior Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical ...
Senior Clinical Study Manager
Chaska, MN · On-site
$135K/yr
The Senior Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical ...
The Senior Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical ...
The Senior Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical ...
The Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical Programs and ...
The Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical Programs and ...
Study Manager
Hoyt Lakes, MN · On-site
$150K - $175K/yr
Description Study Manager NewRange Copper Nickel is searching for a highly motivated and committed individual for our Study Manager position. Reporting to the President & General Manager, the Study ...
Study Manager
Hoyt Lakes, MN · On-site
$150K - $175K/yr
Description Study Manager NewRange Copper Nickel is searching for a highly motivated and committed individual for our Study Manager position. Reporting to the President & General Manager, the Study ...
Advanced Clinical Studies Manager
Stillwater, MN · On-site +1
Design clinical study strategies from the ground up, including selecting appropriate study sites ... Manage and develop clinical teams, providing leadership in clinical management and fostering a ...
New
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Advanced Clinical Studies Manager
Stillwater, MN · On-site +1
Design clinical study strategies from the ground up, including selecting appropriate study sites ... Manage and develop clinical teams, providing leadership in clinical management and fostering a ...
New
The incumbent has responsibility for meeting the milestones of a clinical study in compliance with applicable clinical and regulatory standards and in alignment with the Study Manager as well as ...
The incumbent has responsibility for meeting the milestones of a clinical study in compliance with applicable clinical and regulatory standards and in alignment with the Study Manager as well as ...
Clinical Research Coordinator (Research Professional 2)
Minneapolis, MN · On-site
$25 - $33.65/hr
Lead recruitment efforts for the clinical study, including identification, recruitment, screening ... Under the direction of the PI or study manager, works directly with the study participants and ...
New
Clinical Research Coordinator (Research Professional 2)
Minneapolis, MN · On-site
$25 - $33.65/hr
Lead recruitment efforts for the clinical study, including identification, recruitment, screening ... Under the direction of the PI or study manager, works directly with the study participants and ...
New
Perform remote and on-site monitoring visits at participating clinical study centers to ensure the safety of study patients, the reporting of accurate study data and appropriate study management at ...
New
Perform remote and on-site monitoring visits at participating clinical study centers to ensure the safety of study patients, the reporting of accurate study data and appropriate study management at ...
New
... to clinical study management, site management personnel and site personnel by responding to ... protocol-related issues and escalating as appropriate. • Acts as a primary contact for the ...
New
... to clinical study management, site management personnel and site personnel by responding to ... protocol-related issues and escalating as appropriate. • Acts as a primary contact for the ...
New
Clinical Research Associate II
Minneapolis, MN · On-site
$85K - $105K/yr
Collect and archive study related documentation and correspondence. * Communicate monitoring and site management updates to the internal clinical team. * Assist with the development of the clinical ...
New
Clinical Research Associate II
Minneapolis, MN · On-site
$85K - $105K/yr
Collect and archive study related documentation and correspondence. * Communicate monitoring and site management updates to the internal clinical team. * Assist with the development of the clinical ...
New
Clinical Research Associate II
$85K - $105K/yr
Collect and archive study related documentation and correspondence. * Communicate monitoring and site management updates to the internal clinical team. * Assist with the development of the clinical ...
New
Quick apply
Clinical Research Associate II
$85K - $105K/yr
Collect and archive study related documentation and correspondence. * Communicate monitoring and site management updates to the internal clinical team. * Assist with the development of the clinical ...
New
The Associate Clinical Data Manager is responsible for performing data management tasks within ... Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study ...
The Associate Clinical Data Manager is responsible for performing data management tasks within ... Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study ...
The Associate Clinical Data Manager is responsible for performing data management tasks within ... Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study ...
The Associate Clinical Data Manager is responsible for performing data management tasks within ... Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study ...
The Associate Clinical Data Manager is responsible for performing data management tasks within ... Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study ...
The Associate Clinical Data Manager is responsible for performing data management tasks within ... Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study ...
... management plans and statistical analysis plans * Ensurestimelyandaccuratereporting of study ... Clinical research/clinical trials experience at Medtronic or within a medical device industry
New
... management plans and statistical analysis plans * Ensurestimelyandaccuratereporting of study ... Clinical research/clinical trials experience at Medtronic or within a medical device industry
New
... management plans and statistical analysis plans * Ensurestimelyandaccuratereporting of study ... Clinical research/clinical trials experience at Medtronic or within a medical device industry
New
... management plans and statistical analysis plans * Ensurestimelyandaccuratereporting of study ... Clinical research/clinical trials experience at Medtronic or within a medical device industry
New
Clinical Study Manager information
See Minnesota salary details
$28.25 - $34.25
4% of jobs
$34.25 - $40.24
6% of jobs
$40.24 - $46.23
7% of jobs
$50.73 is the 25th percentile. Wages below this are outliers.
$46.23 - $52.22
9% of jobs
$52.22 - $58.22
15% of jobs
The median wage is $60.86 / hr.
$58.22 - $64.21
18% of jobs
$68.48 is the 75th percentile. Wages above this are outliers.
$64.21 - $70.20
21% of jobs
$70.20 - $76.20
7% of jobs
$76.20 - $82.19
6% of jobs
$82.19 - $88.18
3% of jobs
$88.18 - $94.17
2% of jobs
$28
$61
$94
How much do clinical study manager jobs pay per hour?
As of Aug 6, 2026, the average hourly pay for clinical study manager in Minnesota is $61.23, according to ZipRecruiter salary data. Most workers in this role earn between $49.66 and $68.99 per hour, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as a clinical study manager?
To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.
What are some common challenges faced by clinical study managers, and how can they be addressed?
Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.
What are the most commonly searched types of Clinical Study jobs in Minnesota? The most popular types of Clinical Study jobs in Minnesota are:
What are popular job titles related to Clinical Study Manager jobs in Minnesota? For Clinical Study Manager jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Clinical Study Manager jobs in Minnesota look for? The top searched job categories for Clinical Study Manager jobs in Minnesota are:
- Centralized Monitor Clinical Research
- Overnight Ucsf Clinical Research
- Clinical Research Wearable Devices
- Spaulding Clinical Research
- Volunteer Clinical Studies
- Associate Research Coordinator
- Clinical Trials Ophthalmology
- Temp Clinical Research Coordinator
- Sr Clinical Research Coordinator
- Medical Device Clinical Research Manager
What cities in Minnesota are hiring for Clinical Study Manager jobs? Cities in Minnesota with the most Clinical Study Manager job openings:
Other
Posted 2 days ago
New
Job description
POSITION SUMMARY
This position is for overseeing clinical activities related to one or more clinical studies and performing/managing the daily in-house operations associated with the studies. The Clinical Study Manager must be able to work independently on multiple complex clinical studies using critical thinking skills. This position may be part of a small, cross functional team or may have direct reports.
MAIN DUTIES/RESPONSIBILITIES
- Responsible for managing clinical studies in accordance with internal standard operating procedures and applicable regulations and guidelines
- Collaborate with internal and external clinical team members, consultants and/or CROs to draft clinical study protocols and other clinical study documentation
- Oversee clinical site selection and activation
- Manage study safety by tracking and reporting adverse events as required by regulatory bodies, reviewing adverse event trends, and overseeing safety committees including Clinical Events Committees and Data Safety Monitoring Boards
- Oversee monitoring activities related to assigned clinical studies including review and approval of monitoring plan and monitoring reports, managing monitoring schedule and ensuring corrective action related to monitoring findings
- Develop training plans for study training and review/approve training documentation
- Prepare study-related reports including annual, interim and final study reports
- Organize and lead study-related conference calls and Investigator meetings as needed through the study
- Oversee investigational device allocation, distribution and reconciliation
- Collaborate with data management team and/or CRO to ensure appropriate data capture, query management and to identify data analysis needs
- Use critical thinking skills to review and analyze scientific journal articles
- Assist with generation and/or review of study-related abstracts, posters, presentations, manuscripts as needed
QUALITY SYSTEM RESPONSIBILITIES
- Document product and therapy related field reports within the prescribed timelines and provide any necessary documents required to complete the investigation. Provide follow-up reporting as needed.
- Complete training requirements and competency confirmations as required for this position within the required timeline.
- Comply with applicable quality system procedures/policies and make suggestions for continuous process improvement.
- Ensure all direct reports maintain training records that comply with applicable quality system requirements. (if applicable)
QUALIFICATIONS
Educational Requirements:
- Required: Bachelor's Degree required
- Preferred: Science Degree preferred (Biology, Chemistry, etc.)
Required Experience:
- Previous clinical research experience (minimum 5 years) required
- Previous clinical study management experience preferred
- International clinical experience preferred
- Previous collaboration with physician investigators
- Strong knowledge of clinical research study design and study monitoring functions
- Understanding of GCP and 21 CFR 812
- Experience working with Institutional Review Boards and/or Ethics Committees
- Strong technical writing skills
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About Inspire Medical Systems
Sourced by ZipRecruiter
Industry
Outpatient health care
Company size
201 - 500 Employees
Headquarters location
Golden Valley, MN, US
Year founded
2007