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CRA Consultant Jobs In Minnesota

14 matches | 1 - 14 displayed
date  location  job detail
Dec 31,1969 USA-MN-Plymouth R-D Engineer
Design and redesign medium to high complexity medical devices and subsystems.
Prepare full documentation in accordance with relevant internal SOPs and Design Control.
Participate in pre-clinical in vivo labs, observing cases in hospitals and through planned and unplanned customer i
Nov 07,2018 USA-MN-Fridley Clinical Studies Support Coord II
Job Duties:
Upload study status updates to Vision Tracker application.
Send reminder communication to Principle Investigator to submit study status updates.
Check contract/amendment for expiration and to begin to file in conjunction with Project Manager for contract/amendment extensions.
Contact the
Dec 31,1969 USA-MN-Minneapolis Clinical Research Monitor (CRA)
Job description:
Monitors progress of clinical trials at the site level or headquarters and ensures that they are conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements.
Dec 31,1969 USA-MN-Minneapolis Quality Engineer
? Execute and participate in FMEA/Risk Management activities.
? Serves as a technical resource for problem investigations to guide root cause analysis and corrective action development.
? Contribute to the completion of specific programs and projects.
? Anticipate roadblocks; provide direction for n
Dec 31,1969 USA-MN-Plymouth Senior Clinical Research Specialist
Job description:
Oversees, designs, plans and develops clinical evaluation research studies.
Prepares and authors protocols and patient record forms.
Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial pote
Apr 12,2018 USA-MN-Minneapolis Lab Associate
Clean, prepare, and sterilize processing equipment, and glassware.
Perform manufacturing support activities.
Document/record cGMP data and information for equipment activities, following standard operating procedures. Key documentation includes validation protocols and equipment logbooks.
Perform we
Mar 12,2019 USA-MN-Saint Paul Clinical Specimen Processing Specialist
Saint Paul, MN
What you'll be doing
Receive, identify, and sort packages based on sample type, testing, and client. Recognize and expedite STAT and priority testing; direct samples to appropriate testing area. Open and verify package contents are appropriate for orders sent. Evaluate requests for ac
Feb 14,2019 USA-MN-Arden Hills Clinical Specialist - 64264340 - TT
Job Description:
Our customer is looking for A Clinical Specialist to Support the project team in the planning, execution and management of operational aspects of clinical trials.
? Assists with writing study protocols, protocol amendments, informed consents, clinical study project timelines
Mar 31,2019 USA-MN-Minneapolis Clinical Research PM 954658
Clinical Research PM 954658
Clinical Research PM Duration: 3-6 months Location: remote for the right candidate or Boston/Mpls office The position of Project Manager requires at least a Bachelor s degree, plus a minimum of three (3) years of clinical research experience ma
Jun 22,2019 USA-MN-Saint Paul Medical Laboratory Technician I
Medical Laboratory Technician I
Adecco Staffing
Saint Paul
Job #931446315
A Medical Laboratory Technician I role in Eagan, MN is now available through Adecco Medical and Science. The main function of a lab technician is to perform routine medical laboratory tests for the diagnosis, treatm
Jun 28,2019 USA-MN-Saint Paul Clinical Technologist
Job Description
Pride Health is seeking candidates for an Clinical Technologist position in New Brighton, MN.  This is a 4-5-month assignment, Sun-Thur, 7am-3:30pm.
Receive specimens for testing; evaluate specimens and test orders; determine priority of work and batches to maintain
Jul 01,2019 USA-MN-Minneapolis Clinical Trial Associate
Job Description
Clinical Trial Associate
The Clinical Trial Associate provides clinical study administrative support and Trial Master File (TMF) support for clinical operations. The incumbent also provides support to clinical operations by reviewing vendor invoices for accuracy against budget, track
Jul 07,2019 USA-MN-Arden Hills Clinical Trial Assistant
ICF (Informed Consent Review) experience, IRB experience
Requirements: Bachelor?s degree and 2+ years of related experience or an equivalent combination of education and experience. Background in human clinical study experience required, Clinical Research Coordinator experience preferred.
Jul 10,2019 USA-MN-Mounds View Sr Clinical Research Spec
Key skill looking for in this role will be trial lead 2 clinical research studies.

Responsibilities may include the following and other duties may be assigned. Oversees, designs, plans and develops clinical evaluation research studies. Prepares and authors protocols and patient record forms. Cond
14 matches | 1 - 14 displayed

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