POSITION SUMMARY: This position supports the CIBMTR CRO Services team by supporting the management of one or more multi-center clinical research studies. This position performs site monitoring visits to complete source d…
Skills: Clinical research, Site monitoring, Protocol management, Source document verification, ICH GCP guidelines
Expected Travel: Up to 50% Requisition ID: 13837 About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through ou…
Skills: Clinical Affairs Management, People Management, Medical Device Education, Strategic Planning, Stakeholder Collaboration
Medical Lab Technician (Broadway Family Clinic) - 1.0 FTE
Minneapolis, Minnesota, United States · On-site
$24/hr–$35/hr
Mid level
Why M Physicians? Regardless of role, we recognize that every member of our team is vital! The Medical Lab Technician performs routine clinical laboratory tests ordered by the physicians to assist in patient diagnosis an…
COMPANY OVERVIEW We exist to make food the world loves. But we do more than that. Our company is a place that prioritizes being a force for good, a place to expand learning, explore new perspectives and reimagine new pos…
Core Responsibilities: Patient Management: Diagnosing and treating infections of the ears, nose, throat, larynx, and sinuses by providing patient care at MHealth Fairview Maple Grove Clinic. Surgical Interventions: Perfo…
JOB DETAILS Department: Core Lab FTE: 0.7 (56 hours per pay period) Shift(s): Days (weekdays) // Nights (weekends) // Every Other Weekend Shift Length: 8 hours Location: In-Person Purpose of this position: Under general …
By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researc…
Skills: Assay value assignment, Product validation, Data analysis, Laboratory records management, Batch records maintenance
Data Scientist (Multiple openings) in Minneapolis, MN.
Minneapolis, Minnesota, United States · On-site
$142k–$155k/yr
Senior
At U.S. Bank, we’re on a journey to do our best. Helping the customers and businesses we serve to make better and smarter financial decisions and enabling the communities we support to grow and succeed. We believe it tak…
JOB DETAILS Department: Community Clinics Labs FTE: 0.6 Shift(s): Days Shift Length: 8 hours Location: In-Person This part-time role will work days (start times will fall between 7AM and 10AM). This role will float betwe…
Skills: Phlebotomy, Specimen collection, Specimen processing, Data entry, Electronic health record
The Department of Neurosurgery and the University of Minnesota Masonic Children’s Hospital seek a fellowship trained, board eligible or board certified neurosurgeon with a primary focus in pediatric neurosurgery. This po…
Water Resources Consultant – Senior Level – Mining Focus (Hybrid/Remote)
Duluth, Minnesota, United States · Remote OK
$110k–$160k/yr
Senior+
The role – what you’ll do Barr is seeking a senior water resources consultant with a focus on mine water management to join our team as a mine water practice lead. In this hybrid role, you will work with multidisciplinar…
Skills: Water Balance Modeling, Hydrologic Analysis, Hydraulic Analysis, Mine Water Management, Project Management
We are seeking a full-time Diagnostic Radiologist specialized in Body Imaging to join our very collegial team of 15 system-employed Radiologists, working primarily in downtown Minneapolis at our L1 trauma hospital, Henne…
Skills: Diagnostic Radiology, Body Imaging, Clinical Research, Medical Education, Teaching
Allina Health System, Inc.
Speech Language Pathologist
Minneapolis, Minnesota, United States · On-site
$44/hr–$50/hr
Entry level
Location Address: 2800 10th Ave Receiving Dock Minneapolis, MN 55407-1311 Date Posted: August 10, 2026 Department: 31002000 Courage Kenny Rehabilitation Institute Inpatient Acute Therapy Abbott Northwestern Shift: Day (U…
Skills: Speech Language Pathology, Patient Assessment, Therapeutic Interventions, Clinical Judgment, Communication Disorders
PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requi…
I-2-I Solutions, Inc. (I-2-I) is seeking a Part-Time Water Sampling Technician to collect water and steam condensate samples from designated points of use at the MVAHCS facility. The technician will perform routine and c…
Skills: Water sampling, Water quality testing, Laboratory sampling, Data collection, Recordkeeping
We are seeking a full-time Diagnostic Radiologist specialized in Body Imaging to join our very collegial team of 15 system-employed Radiologists, working primarily in downtown Minneapolis at our L1 trauma hospital, Henne…
Skills: Diagnostic Radiology, Body Imaging, Clinical Research, Medical Education, Teaching
JOB DETAILS Department: Community Clinics Labs FTE: 0.6 Shift(s): Days Shift Length: 8 hours Location: In-Person This part-time role will work days (start times will fall between 7AM and 10AM). This role will float betwe…
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$70k–$85k/yr
Full-time
bachelor degree
Posted 1d ago
Apply by Aug 10
~40 hrs/week
Remote in United States
Responsibilities
This role involves performing remote and on-site monitoring visits to ensure clinical trial compliance and data accuracy. The associate also manages operational aspects of clinical sites, including site activation, document maintenance, and serving as a primary liaison for study personnel.
Requirements
Candidates must have a bachelor's degree in a healthcare or science-related field and at least two years of experience conducting clinical research studies. Proficiency in ICH GCP guidelines, strong communication skills, and the ability to travel 25-50% of the time are required.
Full job description
POSITION SUMMARY: This position supports the CIBMTR CRO Services team by supporting the management of one or more multi-center clinical research studies. This position performs site monitoring visits to complete source document verification and assess site compliance. Additionally, this position is responsible for coordinating and providing support for all aspects of the study including protocol and site management.
ACCOUNTABILITIES: Monitoring: • Perform full-scope remote and on-site monitoring visits involving source document verification, review of essential regulatory documents, and assessing site performance. • Ensure compliance with clinical trial protocols based on regulations, ICH GCP guidelines, and NMDP standard operations procedures. • Identify and communicate site findings with site study personnel and the study team. • Perform query management activities and generate study and site status reports. • With oversight and guidance, analyze trends in identified issues and author visit reports and letters. Ensures documentation and resolution of identified issues and implementation of corrective and preventative action.
Site Management: • Oversee and manage operational aspects of clinical trial sites in conjunction with project teams. • Assists with site activation and ensures study start-up and enrollment goals are met. • Collect and review essential documents for investigational sites, including maintenance of electronic Trial Master File. • Serves as primary liaison for site management issues for assigned studies, escalating to the clinical project manager as required. • Utilizes effective and proactive communication, relationship building, and issue management to develop and maintain good working relationships with Investigators and site staff. • Provide support to Investigators, Study Coordinators, and other appropriate site personnel regarding study workflow, overcoming obstacles and general questions regarding study conduct.
Centralized Monitoring: • Assists in reviewing study site data and data reports to ensure timely and accurate submission and compliance with the study protocol.
Other duties as required for clinical operations: • Performs all duties in compliance with standard operating procedures, regulations outlined in the Code of Federal Regulations (CFR), ICH GCP guidelines, Federal Drug Administration (FDA) guidance and other applicable Federal, state, and local laws. • Assist in user acceptance testing (UAT) of clinical database management system for individual clinical trials. • Performs study tracking (e.g., CTMS, start-up, milestone, closeout); generates, reviews, and distributes management reports from internal tracking systems at requested intervals • Develops, maintains, and presents, in conjunction with senior staff, clinical trial and project specific training materials. • Assists study related problem-solving activities internally and at trial sites. • Assists in protocol maintenance, tracking, and communications. • Works with internal and external team members to deliver high quality trial execution. • Participates in shared team responsibilities, ensuring optimal coverage of trials. • Participates in NMDP, CIBMTR, or CIBMTR CRO Services project teams as needed. • Complete and maintain all training requirements. • Develop, maintain, and continuously improve study and site management processes, guidelines, tools, templates, best practices, and overall implementation. • Other duties as assigned.
REQUIRED QUALIFICATIONS: Knowledge of: • Clinical research study processes, study design, and protocol management. • Medical terminology and anatomy/physiology. • Computer proficiency, including the use of standard software (word processing, databases, e-mail) and the use of internet. • Training and conflict resolution skills. • Time management skills and problem-solving abilities.
Ability to: • Demonstrate excellent oral and written communication. • Manage multiple deadlines and priorities while ensuring quality and timeliness. • Perform tasks requiring excellent attention to detail. • Demonstrate independent problem-solving and decision-making for straightforward situations, but requires guidance for complex situations. • Analyze trends, identify issues, and escalate as appropriate. • Adapt to change. • Navigate processes and people involved in clinical research, demonstrating organizational awareness and interpersonal skills necessary to complete work efficiently. • Travel 25-50%, both domestic and international, depending on assigned studies. Travel at times may increase up to 70% as required. • Must exemplify our NMDP values in a highly professional manner in all settings.
Education and/or Experience: • Bachelor’s degree in healthcare/science related field; however, upon evaluation, equivalent related experience and/or education may be substituted for the scientific or health-related degree requirement. • Minimum two years’ experience of conducting clinical research studies according to ICH GCP guidelines and/or verifying clinical data from medical records.
PREFERRED QUALIFICATIONS: (Additional qualifications that may make a person even more effective in the role, but are not required for consideration) • Knowledge of cellular therapies, diseases treated by cellular therapies, disease assessments, and common treatment complications. • Direct experience working at research sites on clinical studies, with or without direct interaction with patients. • ACRP or SOCRA certification.
Introducing NMDP, formerly known as the National Marrow Donor Program and Be The Match. Our name has changed but our mission has not: We save lives through cell therapy.
At NMDP, we believe each of us holds the key to curing blood cancers and disorders. As a global nonprofit leader in cell therapy, NMDP creates essential connections between researchers and supporters to inspire action and accelerate innovation to find life-saving cures. With the help of blood stem cell donors from the world’s most diverse registry and our extensive network of transplant partners, physicians and caregivers, we’re expanding access to treatment so that every patient can receive their life-saving cell therapy.
NMDP. Find cures. Save lives.
Learn more about our career opportunities at www.nmdp.org/what-we-do/about-us/careers
Offices: 500 N 5th St, Minneapolis, Minnesota 55401, US
How many Science & Research jobs are open in Minneapolis, MN right now?
There are currently 490 open science & research positions in Minneapolis, MN listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Minneapolis, MN?
Companies currently hiring include Hennepin Healthcare, Children's Minnesota, Fairview Health Services, Allina Health System, Inc., Lunaphore (a Bio-Techne brand), among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Minneapolis, MN?
Yes — 122 of the 490 open science & research positions offer remote or hybrid work (55 remote, 67 hybrid).
How do I apply for Science & Research jobs in Minneapolis, MN?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.