Clinical Project Specialist
Benefits
Unlimited PTO
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Key Responsibilities:
- Document and manage study plans, essential documents, and site activation from start-up through close-out.
- Oversee TMF quality, inspection readiness, and coordinate with vendors and cross-functional teams.
Qualifications:
- 2-4 years of progressive clinical research experience with knowledge of FDA regulations and ICH-GCP.
- Proficiency in MS Office, eTMF, and exceptional attention to detail.
What We Offer:
- Full medical, dental, and vision insurance for you and your family.
- Flexible PTO and a 401(k) plan with company match.
- Opportunities for growth and a supportive team environment.
ProTrials
ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. They are a collaborative community committed to making a meaningful impact on global health, valuing team members and empowering them.