Top 45 Clinical project manager Jobs in Maple Grove Mn

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
1d
Clinical Project Manager
Meditrial Europe Ltd. —Minneapolis, MN
- Full-time
- 6 years
- Master's degree
- Bachelor's degree
3d
Clinical Research Project Coordinator V
Medtronic —Mounds View, MN
- $75,200 - $112,800 a year
- Full-time
- Office
- High school diploma or GED
- US work authorization
- Health savings account
- Employee stock purchase plan
8d
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
Quick Apply
1d
Manager, Global Clinical Trial Operations
Boston Scientific —Arden Hills, MN
- $102,100 - $194,000 a year
- Hybrid work
- 7 years
- Office
- Bachelor's degree
Clinical Trial Manager
Coloplast —Minneapolis, MN
- $108,191 - $162,287 a year
- Hybrid work
- Microsoft Excel
- Databases
- Bachelor's degree
- Paid parental leave
- Dental insurance
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
Quick Apply
Implementation Manager
AssistIQ —Minneapolis, MN
- Full-time
- Remote
- Mid-level
- Driver's License
- Continuous improvement
- Health insurance
- Flexible schedule
Quick Apply
Clinical Data Manager
Meditrial Europe Ltd. —Minneapolis, MN
- 5 years
- Office
- Master's degree
5d
Senior Manager, Clinical Operations
Zoll Medical Corporation —Minneapolis, MN
- $150,000 - $175,000 a year
- Hybrid work
- Office
- 3 years
- Bachelor's degree
Clinical Research Associate (CRA) II
CVRx, Inc. —Brooklyn Park, MN
- $85,000 - $105,000 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 Project Specialist
University of Minnesota —Minneapolis, MN
- Weekends as needed
- Hybrid work
- Microsoft Word
- Background check
- Surgery
Clinical Research Coordinator
University of Minnesota —Minneapolis, MN
- Weekends as needed
- Background check
- Computer literacy
- 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
New Product Introduction Project Manager (MedSurg)
Solventum —Eagan, MN
- $143,200 - $196,900 a year
- Full-time
- Hybrid work
- Engineering
- English
- Office
- Health savings account
- Disability insurance
Marketing Operations Manager
AtriCure —Minnetonka, MN
- $81,000 - $120,000 a year
- Background check
- Microsoft Excel
- Marketing
- Paid parental leave
- Health insurance
Senior Medicaid Program Health Manager OR Medicaid Program Health Manager
Blue Cross and Blue Shield of Minnesota —Eagan, MN
- $79,100 - $149,800 a year
- Hybrid work
- Office
- Bachelor's degree
- Senior level
- Health insurance
- Dental insurance
Department of Orthopedic Surgery Clinical Research Coordinator- Research Professional 2
University of Minnesota —Minneapolis, MN
- Online Application
- Background check
- Management
- Surgery
Software Project Manager
HISTOSONICS INC —Plymouth, MN
- $135,000 - $180,000 a year
- Full-time
- Computer science
- Computer Science
- Bachelor's degree
- Disability insurance
- Dental insurance
Quick Apply
Hospital Program & Mobile Operations Coordinator
Parsons —Minneapolis, MN
- $30.58 - $53.51 an hour
- Clean driving record
- Writing skills
- HIPAA
- Wellness program
- Paid holidays

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Associate Clinical Data Manager

Abbott Laboratories -
Maple Grove, MN

Apply Now

Job Details

Full-time
$61,300 - $122,700 a year
1 day ago

Benefits

Health insurance
Tuition reimbursement
Retirement plan

Qualifications

Anatomy knowledge
Technical documentation
Data structures
Clinical quality assurance standards
Medical terminology
FDA regulations

Full Job Description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

Career development with an international company where you can grow the career you dream of.

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

An excellent retirement savings plan with high employer contribution

Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.

A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ﬁnger sticks.

The Opportunity - CAN CHANGE

Our location in Maple Grove MN currently has an on-site opportunity for an Associate Clinical Data Manager. The Associate Clinical Data Manager is responsible for performing data management tasks within defined established processes throughout the life cycle of the study including startup, conduct and reporting phases.

What You’ll Work On - CAN CHANGE

Works with Data Review Manager in the study start-up and planning, including contributing to the development of the Risk Assessment and Risk Mitigation Plan, Data Management Plan, Central Monitoring Plan and Data Review Plan.

Translates Clinical Study requirements into technical requirements for eCRFs, edit checks, study notifications and customizations in the study database in close collaboration with other member of the data review team.

Able to develop CRF with cross functional support, incorporating appropriate feedback and finalizing the CRF.

Able to develop specifications for data listings for continuous data review, and communicate with data analytics team members through their development and release.

Able to work with external non-CRF data, including developing creating Data Transfer Specifications, verification of external data structure for import into the data model.

Able to develop edit check specifications to review for illogical, incomplete and inconsistent data including testing and troubleshooting of edits checks.

Identifies, analyzes, proposes solutions, and effectively resolves complex data/database structure issues by exercising appropriate judgment and collaborating with the clinical project team members and other shared service functions.

Contributes to the development and maintenance of Clinical Database systems, including EDC, Edit Checks, Reporting, Study Notifications, etc. through the following:

Partner closely with Data Review Management, Study Database Manager, and Data Analytics and Systems and other Data Review team members.

Perform and document functional and/or user acceptance testing on study databases, reports, study notifications, and database customizations.

Utilize existing tools/reports,SQL, and database UI to identify data issues and drive resolutions with the Clinical Study Team in a timely manner.

Attend Clinical Study Team meetings.

Contribute technical expertise to cross functional teams through CRF changes and the impact on databases and propose implementation strategies.

Assists in FDA and Quality System audits that involve Clinical Database and Data Management

Follows data management standards and best practices and assures Standard processes are followed for Data Management activities.

Contribute to data cleaning and data snapshot efforts for regulatory submissions and other business needs as requested by the Clinical Study Team through the following:

Generate database snapshot and prepare datasets for Biometrics.

Contribute to data review meetings with the Clinical Study Team and Biometrics to identify data cleaning issues and strategize cleaning efforts.

Monitor overall data management tasks to ensure that timelines are met and that any issues are proactively identified and resolved.

Perform other duties as assigned.

Required Qualifications – CAN’T CHANGE

Bachelor’s degree in a related field OR an equivalent combination of education and work experience.

Minimum 3 years’ in clinical, medical or research setting.

Education and work experience in computer science, life sciences or technical field.

Knowledge of data collection best practices for clinical trials.

Knowledge of global clinical operations.

Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device.

Intermediate medical knowledge related to common medical histories, medical terminology, diagnostics (imaging, laboratory), and medications (class, dose, route).

Certified Clinical Data Manager (CCDM) or equivalent.

Preferred Qualifications – CAN CHANGE

Bachelor’s degree in business administration, data science, statistics or life sciences.

3 years’ experience in clinical operations or healthcare related field.

Knowledge of data management practices from CRF design to database development and study closure.

Experience with using Electronic Data Capture (EDC) databases and advanced skill level working in Excel.

Knowledge of documentation practices in-line with Good Clinical Data Management Practices, and other FDA regulations and guidelines is required.

Ability to leverage and/or engage others to accomplish projects.

Solid oral and written communication skills and analytical/problem-solving skills.

Must be able to effectively manage multiple projects and timelines.

Requires the ability to sit or stand while working on a computer for a long period of time.

The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted.

Apply Now

Refine Your Search

clinical project manager jobs in maple grove mn

Associate Clinical Data Manager

Clinical Project Manager

Clinical Research Project Coordinator V

Clinical Project Manager

Manager, Global Clinical Trial Operations

Clinical Trial Manager

Clinical Research Manager

Implementation Manager

Clinical Data Manager

Senior Manager, Clinical Operations

Clinical Research Associate (CRA) II

Clinical Research Project Specialist

Clinical Research Coordinator

Clinical Research Coordinator

New Product Introduction Project Manager (MedSurg)

Marketing Operations Manager

Senior Medicaid Program Health Manager OR Medicaid Program Health Manager

Department of Orthopedic Surgery Clinical Research Coordinator- Research Professional 2

Software Project Manager

Hospital Program & Mobile Operations Coordinator

I want to receive the latest job alert for clinical project manager in maple grove mn

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