Clinical Research Assistant
About The Position
This role reports to the Clinical Manager and is part of a new team with the Eurofins network, supporting Phase I-III IND clinical trials with Hair, Skin and Nail evaluation endpoints. We will train the right candidate but experience in any discipline of Clinical research (especially from a regulatory aspect) is a plus. You will work closely with a small team inclusive of 2 Principal Investigators in Dermatology. Clinical Research Assistant responsibilities include, but are not limited to, the following: Project support inclusive of project planning, Preparation of paperwork and documentation, and maintaining study participant records. Data collection Audits (both virtual and in person) General preparation and closing of studies Working with IRB submissions Assisting with Study participant recruitment inclusive of phone and in person screening and subject scheduling Executing Study participant visits inclusive of subject vitals (possibly Phlebotomy but will train) , electronic data entry, visual evaluations and PI assistance. Clinical Trial data entry Other tasks as dictated by business needs and the Clinical Manager
Requirements
- Certified CRA credential ideal
- Minimum 1+ years expereince in clinical research
- Experience in regulatory aspects of Phase I-III clinical IND trials and experience with FDA audits.
- Experience with Microsoft platforms, EMR and EHR (electronic health record) systems and CTMS strongly preferred.
- Experience with phlebotomy preferred.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Nice To Haves
- Certified CRA credential ideal
- Experience with phlebotomy preferred.
- Experience with Microsoft platforms, EMR and EHR (electronic health record) systems and CTMS strongly preferred.
Responsibilities
- Project support inclusive of project planning
- Preparation of paperwork and documentation
- Maintaining study participant records
- Data collection
- Audits (both virtual and in person)
- General preparation and closing of studies
- Working with IRB submissions
- Assisting with Study participant recruitment inclusive of phone and in person screening and subject scheduling
- Executing Study participant visits inclusive of subject vitals (possibly Phlebotomy but will train)
- Electronic data entry
- Visual evaluations and PI assistance
- Clinical Trial data entry
- Other tasks as dictated by business needs and the Clinical Manager
Benefits
- comprehensive medical coverage
- dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
