Clinical Research Protocol Specialist
1 week ago
Position:
Clinical Research Protocol Specialist
Location:
Remote with occasional in-office collaboration
Contract Duration:
6 Month Contract-to-Hire
Working Hours:
Monday to Friday, 8:00 AM - 4:30 PM
Qualifications:
- Bachelor’s degree in Life Sciences or a related field
- 1-2 years of experience in research within a Pharmaceutical, Clinical Research Organization, Biotechnology, or Healthcare environment (Co-Op and Internship experience will be considered)
- Openness to training opportunities for the right candidate
- Proficient in Microsoft Office Suite
- Familiarity with Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), and Adobe Acrobat is preferred but not mandatory.
- COVID-19 vaccination is required
Key Responsibilities:
- Assist the department with daily administrative project tasks.
- Provide guidance to sites regarding protocol execution, interpretation of protocols, and facilitate issue resolution as necessary.
- Assess data quality, manage queries, and implement corrective action plans as needed.
- Develop presentation materials for both internal and external meetings.
- Maintain and update internal databases, tracking systems, and project plans with department and trial-specific information.
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