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About ProTrials:
- Women-owned CRO operating since 1996.
- Committed to high-quality, ethical clinical research services.
- Offers a collaborative and supportive team culture.
Responsibilities:
- Act as primary liaison between CRAs, internal staff, site staff, clients, and vendors.
- Develop and manage clinical plans, timelines, and monitoring compliance.
- Oversee TMF/eTMF and ensure quality control of study documents.
Qualifications:
- RN, Bachelor’s, or advanced degree in biological sciences or related field.
- Previous CRA experience preferred with strong communication and organizational skills.
- Extensive knowledge of FDA regulations and proficiency in Microsoft Office.
Compensation:
- Salary range $135,000 - $159,000 per year, based on experience and location.
- Remote home-based position with occasional travel for site visits.
ProTrials
ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) trusted since 1996, delivering ethical services to pharmaceutical, biotech, and medical device companies. They foster a collaborative community where team members feel valued and empowered to make a meaningful impact on global health.