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Senior Research Associate Institution: Location:Milwaukee, WI Category: Admin Institutional Research and Planning Admin Assessment, Accreditation, and Compliance ...
Clinical Research Coordinator I MCW Department: Pathology Division: Position Number: 322.32065 Location.: Dynacare Lab Building Work Hours: 8am5pm; duties ...
monitoring pharmaceutical clinical trials. Previous... job tenure within their CRA positions overall and steady progression within the CRA career ladder with the......
monitoring pharmaceutical clinical trials. Previous... job tenure within their CRA positions overall and steady progression within the CRA career ladder with the......
75% Our Clinical Research Associates manage all aspects of site monitoring responsibilities for Clinical... visits). •3 years clinical research experience in the......
For your reference, we have included the original job posting below.
Clinical Research Associate (CRA)
Job Number:
26850754
Company Name:
Aerotek Scientific
Job Location:
Milwaukee, WI US
Job Category:
Research
Clinical Research Associate (CRA)
A large Healthcare and Medical Device company located in Milwaukee, Wisconsin is looking for a qualified Clinical Research Associate (CRA) to join their team Clinical Research Associate (CRA) monitors and coordinates clinical research studies at external trial sites in compliance with Good Clinical Practice, Standard Operating Procedures, and Corporate Policies, Guidelines and Standards. Major job duties include: - Contributes to the preparation of study documentation such as Protocols, Amendments, Case Report Forms (CRFs) and Clinical Study Reports (CSRs).- Collects and processes Regulatory and Ethics Committee documents and correspondence- Maintain awareness of Good Clinical Practice Guidelines, Quality Manuals, Quality Management Systems, Quality Management Policies, Quality Goals, and applicable laws and regulations.- Complete all planned Quality & Compliance training within the defined deadlines.- Identify and report any quality or compliance concerns and take immediate corrective action as required.- Execute Company sponsored clinical research trials that are compliant with internal procedures and GCP guidelines.- Assist with continuous improvement activities by driving the implementation of process and product quality improvement requirements and qualifications:- Bachelors Degree- 1-3 Years of experience in Clinical Research and/or Clinical Trials.- Medical Device, Pharmaceutical, or CRO industry experience.- Prior experience with Trial Master File (TMF) or Clinical History Files (CHF) strongly preferred.- Prior experience as a Clinical Research Associate (CRA), Clinical Research Coordinator (CRC) or Documentation Specialist strongly you are interested in learning more about this opportunity please contact Greg Painter directly at . Category: Medical Sciences
