**Job Description**
This position involves comprehensive support for clinical trials, focusing on data management, document handling, query resolution, and subject reimbursement. Responsibilities include data entry into electronic data capture (EDC) systems and OnCore, maintaining subject and regulatory binders, resolving data queries, and managing subject travel expenses and stipends while ensuring data consistency and communication with external stakeholders.
**Skills & Abilities**
• Detail oriented
• Excellent time management skills
• Coordinate multiple tasks
• Work independently and productively in a fast paced, deadline-oriented environment
• Excellent interpersonal skills
• Ability to effectively communicate verbally and in writing
• Ability to collaborate with faculty and staff at multiple levels
• Maintain working relationships with company representatives
• Proficiency with Word, Excel, Adobe, OnCore, and various clinical research EDC platforms
• Prior clinical research experience
**Qualifications**
Required Degree(s) in:
• High school diploma or equivalent
**Experience**
Experience Required:
• 1 year of relevant experience (with high school diploma or equivalent)
Other:
• Health Assessment Required
• Eligibility for veteran’s preference
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