Research Coordinator I
New
C
COG Research Foundation, LLC Clinical Research
Employee must reside within the United States.Full-TimeEntry
Salary64,542 - 92,421 USD per year
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Job Details
- Experience
- Two (2) years of human clinical trial research experience.
- Required Skills
- Microsoft Office
Requirements
- Bachelor’s degree in a related field, or substitute with four additional years of relevant experience.
- Two years of human clinical trial research experience (or a combination of relevant master’s degree and experience).
- Strong organizational skills and ability to work independently.
- High level of PC literacy, including proficiency in MS Office (Word, Excel, PowerPoint).
- Excellent written and oral communication skills.
- Critical thinking and reasoning abilities.
- Experience as a Clinical Data Manager or Clinical Research Coordinator is preferred.
- Experience in a comprehensive cancer center, cooperative group, or pharma/biotech industry is highly desirable.
Responsibilities
- Review study protocols and design CRFs and data validations to meet study aims.
- Coordinate CRF development and study set-up with study committees and teams.
- Construct CDISC/CDASH variables and fragments adhering to SOPs.
- Perform User Acceptance Testing within the study EDC.
- Create and maintain an integrated study data management plan (DMP).
- Monitor active trials, including subject enrollments/randomizations and study status updates.
- Ensure data quality and timeliness of institutional submissions.
- Resolve data-related issues, queries, and discrepancies in collaboration with study teams.
- Ensure Serious Adverse Events (SAE) reporting complies with protocol and NCI guidance.
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