Data Entry Coordinator - CenExel Clinical Research
Overview
The Data Entry Coordinator will own clinical research data entry at CenExel Clinical Research. This role operates under moderate supervision within a team focused on quality people teamwork and optimal work-life balance. Candidates should thrive in a fast paced environment and enjoy collaborative settings.
What You'll Do11
- 1Ensures timely data entry through department and study tracking systems
- 2Maintains professional relationships with Clinical Operations Quality Regulatory teams and CROs
- 3Transcribes data accurately and efficiently from source documents to electronic data capture
- 4Assists in preparing for internal and external data audits with clinical operations quality and regulatory teams
- 5Completes training and obtains applicable certificates and access to CRFs and EDCs
- 6Verifies source documents using buddy checks
- 7Supports Clinical Research Coordinators in entering paper source documents to eCRFs
- 8Adheres strictly to FDA CFR ICH GCP and CenExel SOPs
- 9Follows company guidelines protocols and site working practices
- 10Assumes additional duties as assigned
- 11Supports overall data integrity across multiple clinical trials
Requirements9
- 1High school diploma or equivalent with one year of data entry experience preferred
- 2Excellent computer skills and medical research terminology knowledge
- 3Self directed ability to work with minimal supervision
- 4Bilingual English Spanish proficiency required
- 5Clinical background with psychiatric experience preferred
- 6Ability to manage multiple projects and responsibilities
- 7Physical stamina for sitting typing standing and walking
- 8Lightly active position with occasional lifting of twenty pounds
- 9Reliable attendance and onsite reporting schedule
Salary Insight
Salary not disclosed in listing
Location
Required Skills
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