Data Entry Specialist

Role Overview

Key Responsibilities

• Organize and interpret data from clinical trials, ensuring timely and accurate data entry into paper or electronic forms.
• Review source documents and case report forms to identify and resolve data discrepancies.
• Communicate effectively with team members and clients regarding study-related inquiries and requests.
• Audit and organize source documents post-trial, ensuring completeness before archiving.
• Manage study-specific information efficiently to support regulatory reporting and documentation standards.

Qualifications And Skills

• High School diploma or equivalent; experience in data management preferred.
• Knowledge of Microsoft Office and data management processes.
• Strong organizational, time management, and communication skills.
• Ability to work independently and collaboratively.
• Physical ability to perform tasks involving bending, lifting, and prolonged sitting.

Additional Information

• The role offers benefits including health insurance, paid time off, bonuses, and promotes work/life balance.
• Candidates should adhere to equal opportunity employment standards.