Top 18 Clinical trial manager Jobs in Maple Grove, Mn

Clinical Project Manager
Laborie Medical Technologies Corp —Minnetonka, MN
- $130,000 - $135,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Doctoral degree
- Health savings account
- Health insurance
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Clinical Research Manager
Minneapolis Heart Institute Foundation —Minneapolis, MN
- $115,000 - $125,000 a year
- Part-time
- Bachelor's degree
- Organizational skills
- Experience equivalent to degree accepted
- Health savings account
- Paid holidays
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Senior Manager, Clinical Studies
Inspire Medical Systems Inc. —Minneapolis, MN
- $140,000 - $180,000 a year
- 5 years
- Bachelor's degree
- Continuous improvement
- Health savings account
- Employee stock purchase plan
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7d
Senior Manager, Clinical Studies
Inspire Medical Systems —Minneapolis, MN
- $140,000 - $180,000 a year
- 5 years
- Bachelor's degree
- Continuous improvement
- Health savings account
- Employee stock purchase plan
Senior Manager, Clinical Operations
Zoll Medical Corporation —Minneapolis, MN
- $150,000 - $175,000 a year
- Hybrid work
- Office
- 3 years
- Bachelor's degree
Manager, Clinical Data Review
Abbott Laboratories —Maple Grove, MN
- $99,300 - $198,700 a year
- Full-time
- Word processing
- 8 years
- Bachelor's degree
- Health insurance
- Tuition reimbursement
Research Manager 2 - Clinical Research Project Management
University of Minnesota —Minneapolis, MN
- Online Application
- Background check
- 6 years
- Psychiatry
Clinical Specialist Manager
VivaQuant, Inc. —Arden Hills, MN
- $120,000 - $140,000 a year
- Full-time
- Nursing
- Management
- Up to 50% travel
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Clinical Project Manager
Meditrial Europe Ltd. —Minneapolis, MN
- Full-time
- 6 years
- Master's degree
- Bachelor's degree
Associate Clinical Data Manager
Abbott Laboratories —Maple Grove, MN
- $61,300 - $122,700 a year
- Full-time
- Computer science
- Anatomy knowledge
- Computer Science
- Health insurance
- Tuition reimbursement
Senior Clinical Study Manager
Beckman Coulter Diagnostics —Chaska, MN
- $125,000 - $135,000 a year
- Full-time
- Doctoral degree
- 3 years
- Master's degree
- Health insurance
- Dental insurance
Manager, Clinical AI Partnerships & Integration
VIDA Diagnostics —Edina, MN
- $120,000 - $150,000 a year
- Computer science
- Computer Science
- 5 years
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Senior Clinical Marketing Manager, Interventional (REMOTE)
Teleflex —Maple Grove, MN
- $132,900 - $199,400 a year
- Up to 50% travel
- Bachelor's degree
- Travel
- Disability insurance
- Health insurance
Clinical Data Manager
Meditrial Europe Ltd. —Minneapolis, MN
- 5 years
- Office
- Master's degree
Senior Manager, Study Data Architecture (on-site)
Abbott Laboratories —Maple Grove, MN
- $113,300 - $226,700 a year
- Full-time
- 7 years
- Computer Science
- Quality control
- Health insurance
- Tuition reimbursement
Medical Imaging Supervisor
University of Minnesota —Minneapolis, MN
- Online Application
- Background check
- Patient monitoring
- Word processing

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Clinical Project Manager
Laborie Medical Technologies Corp —Minnetonka, MN
Ensure all project level study documentation is filed in the TMF in accordance with company SOPs/all regulatory requirements and provide oversight to the…
$130,000 - $135,000 a year
Quick Apply
Clinical Research Manager
Minneapolis Heart Institute Foundation —Minneapolis, MN
At times, may serve as an individual contributor assisting in study design, implementation, and administration, ensuring compliance with HRRC (IRB) requirements…
$115,000 - $125,000 a year
Quick Apply

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Senior Local Trial Manager (Sponsor Dedicated, Multiple Therapeutics)
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Degree in a health or science-related field. This may require development of local trial-specific procedures and tools, recruitment planning, contingency and…
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Conduct comprehensive patient assessments, diagnostic evaluations, and develop individualized treatment plans aligned with best practices in mental health,…
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Clinical Project Manager

Laborie Medical Technologies Corp -
Minnetonka, MN

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Job Details

Full-time
$130,000 - $135,000 a year

Benefits

Health savings account
Health insurance
Dental insurance
Flexible spending account
Paid time off
Adoption assistance
Parental leave
Vision insurance
401(k) matching

Qualifications

Medical writing
Microsoft Excel
Microsoft Outlook
English
ICH guidelines
Bachelor's degree
Data management
Microsoft Teams
Clinical quality assurance standards
Healthcare research
FDA regulations

Full Job Description

We believe that great healthcare is an essential safeguard of human dignity.

At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you.

We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.

Who We’re Looking For:

As a key member of the Clinical team, the Clinical Project Manager (CPM) is responsible for the management of all aspects of Clinical Trial Team activities for assigned project(s). The CPM, in concert with the Clinical Program Manager, is accountable for achieving successful delivery of Laborie Clinical Team activities at the project level by meeting company and regulatory requirements according to time, quality/scope, and budget constraints.

About the Role:

Proactively manage project level operational aspects of Clinical Research Team (CRT) including management of trial timeline, budget, resources, and vendors.
Provide efficient updates on trial progress to the Clinical Program Manager and/or Chief Technology Officer, with respect to vendor selection, project plans, trial budget and timeline management, quality standards and risk mitigation.
Lead sponsor study startup process, including but not limited to conduct of the Trial Kick-off meeting, the setup of trial master file (TMF), site selection and finalization of site and vendor Clinical Trial Agreements and budgets.
Ensure effective project plans are in place and operational for each trial and work proactively with the Clinical Research Team to set priorities in accordance with applicable project plans, company standard operational procedures (SOPs), ICH/GCP guidelines and regulatory requirements.
Chair Clinical Research Team working group and vendor status update meetings and ensure meeting minutes are completed, distributed to team members, and filed in the Trial Master File (TMF) in a timely manner.
Monitor the quality of vendor deliverables, address quality issues with the appropriate team member and identify opportunities to improve training, execution, and quality control across the clinical team.
Review and approve vendor invoices in collaboration with the accounting team to ensure investigator payments occur in a timely manner.
Ensure all project level study documentation is filed in the TMF in accordance with company SOPs/all regulatory requirements and provide oversight to the clinical team regarding TMF filing, maintenance and archival procedures
Effectively provide support to the Clinical Research Team in the conduct of the trial(s).

Minimum Qualifications:

Bachelor's degree in Life Sciences; Master's or Doctoral degree preferred.
8+ years of clinical operations experience for CPM; with increasing levels of responsibility in the medical device or CRO industry is required.
Minimum 2 years of clinical project management experience at a sponsor or CRO company is preferred.
Therapeutic/intervention experience in urogynecology, gastroenterology, and/or OB/GYN.
Experience with medical devices CER, PMS, PMCF, PSUR medical writing.
Speak fluent English, excellent verbal and written communication skills, Microsoft Office, Excel, PowerPoint, Outlook, Teams, etc.
Must have thorough knowledge of clinical research concepts, practices, and FDA/EU regulations and ICH Guidelines, ISO 14155, clinical research, and data management methods.

Why Laborie:

Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.

Paid time off and paid volunteer time
Medical, Dental, Vision and Flexible Spending Account
Health Savings Account with Company Funded Contributions
401k Retirement Plan with Company Match
Parental Leave and Adoption Services
Health and Wellness Programs and Events
Awarded 2025 Cigna Healthy Workforce Designation Gold Level

Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.

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clinical trial manager jobs in maple grove, mn

Clinical Project Manager

Clinical Research Manager

Senior Manager, Clinical Studies

Senior Manager, Clinical Studies

Senior Manager, Clinical Operations

Manager, Clinical Data Review

Research Manager 2 - Clinical Research Project Management

Clinical Specialist Manager

Clinical Project Manager

Associate Clinical Data Manager

Senior Clinical Study Manager

Manager, Clinical AI Partnerships & Integration

Senior Clinical Marketing Manager, Interventional (REMOTE)

Clinical Data Manager

Senior Manager, Study Data Architecture (on-site)

Medical Imaging Supervisor

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