Clinical Operations Specialist
Lexitas
full-time
Posted on:
Location Type: Remote
Location: United States
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Salary
💰 $78,000 - $83,000 per year
About the role
- Provides support to Study Management and other study team members
- Responsible for in-house site management
- Manages all protocol-level and investigator-related clinical trial documents, study supplies, and vendor information
- Keeps study-related essential documentation current and filed
- Facilitates collection and review of essential documents, budgets/contracts, and IRB documentation on behalf of sponsor and site.
Requirements
- BA/BS in a science/health care field, nursing degree, or equivalent combination of education and experience
- At least 1 to 2 years of clinical research coordinating experience or experience working in a contract research organization (CRO) or pharmaceutical or biotechnology company is preferred
- Competent computer skills including MS Office Suite
- Experience working with eTMF and EDC systems is preferred
Benefits
- Health insurance
- 401(k) matching
- Flexible work hours
- Paid time off
- Remote work options
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical research coordinationprotocol managementdocument managementbudget managementcontract managementIRB documentationeTMFEDC systems
Soft skills
supportorganizationcommunication
Certifications
BA/BS in sciencenursing degree