Data Entry Coordinator
On-siteFarmington, Michigan, United States
Job Summary
Manage data entry into computer systems for clinical trials, including entering patient data into eDC and other software. Review patient charts and medical records to ensure timely data entry in accordance with eCRF guidelines and protocol requirements. Collaborate with site teams to report irregularities or problems with a study to appropriate parties. Maintain confidentiality of sensitive information in compliance with HIPAA and GCP regulations. Ensure execution of assigned studies while adhering to SOPs, FDA, and ICH regulations. Requires at least one year of clinical data entry experience, proficiency in Microsoft applications, and a typing speed of 40+ wpm. Full-time employees work at least 30 hours per week and are eligible for medical, dental, vision, and 401k benefits.
Required Qualifications
- High School diploma or equivalent
- minimum of 1 year of clinical data entry experience
- equivalent combination of education and experience
- Proficiency with computer applications such as Microsoft applications, email, and web applications
- ability to type proficiently (40+ wpm)
- Strong organizational skills and attention to detail
- Well-developed written and verbal communication skills
- Well-developed interpersonal and listening skills
- ability to work well independently as well as with co-workers, subjects, managers and external customers
- Ability to effectively handle multiple tasks
- adapt to changes in workloads and priorities
- professional
- respectful of others
- self-motivated
- strong work ethic
- high degree of integrity and dependability
- Ability to handle highly sensitive information in a confidential and professional manner
- compliance with HIPAA guidelines
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