Talascend is seeking a professional, skilled individual for our Clinical Research Associate position located in Wauwatosa, WI.
Essential Responsibilities
Duties include (but are not limited to) :
- Recruit, screen, enroll, and obtain informed consent from study participants
- Coordinate and oversee research sessions, including scheduling participants, reserving space, ensuring staff training, and managing documentation
- Ensure compliance with the study protocol, external standards (regulations, GCP, IRB requirements), and internal GEHC processes
- Maintain all study documentation, including regulatory binders, source documentation, trackers, and other materials
- Complete IRB submissions such as new study submissions, Continuing Review, Amendments, Deviation reports, and Adverse Event reports
- Conduct training and provide guidance to a large study staff
- Facilitate regular monitoring visits; prepare for audits as needed
- Serve as main point of contact for research volunteers and study staff
- Maintain facilities (consent area, scan bays), order supplies and track spend
- Implement process improvement activities as needed
- Implement electronic processes to facilitate compliance and efficiency
- Provide support to Research Program Integrators as needed
- Serve as a Subject Matter Expert (SME) for coordinators at global sites executing similar protocols
Qualifications / Requirements :
- Bachelor's degree in science or research-related field
- Previous experience with a minimum of 2 years in clinical research
- Outstanding organizational skills
- Proficient at Microsoft Office (Excel, Outlook, Word)
- Meticulous attention to detail
- Exceptionally well-organized
- Excellent communication skills (written and verbal)
- Must be willing to work in our Wauwatosa, WI facility
Desired Characteristics :
- CCRC or CCRP certified preferred
- Previous experience as a Clinical Research Coordinator
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