Clinical Data Entry Coordinator — Research & Trials

Evolution Research Group; Bellaire (TX); On-site; USD 36,000 - 48,000; Full time

Benefits offered by this job

Medical and dental coverage

401(k) matching

Paid time off

Job summary

Evolution Research Group seeks a detail-oriented Data Entry Coordinator to manage clinical data entry procedures under the Site Director’s guidance. You will maintain confidential study files, ensure data completeness, and comply with GCP/ICH guidelines and ERG SOPs across studies.

Responsibilities include accurate data entry, quality control, and timely resolution of data queries in collaboration with CRC, Sponsors, or CROs, ensuring high data quality in a fast-paced clinical environment.

Qualifications

• High school diploma or equivalent.
• Proven experience in data entry or a related field.
• Proficiency in word processing and database applications.
• Excellent attention to detail and accuracy.
• Strong organizational and time management skills.

Responsibilities

• Performing data entry tasks with a high degree of accuracy and efficiency.
• Responsible for clinical data processing as directed by Site Director or another assigned manager; QC data and report discrepancies.
• Complete any training as required by sponsor for access and approval to complete data entry.
• Enter data for protocol into paper or electronic case report forms.
• Track to ensure data entry is complete for subjects including completed study visits and related forms.
• Assist Sponsor or CRO data manager with resolution of queries to ensure clinical data quality.
• Study, learn, and comply with ERG SOPs and policies.

Skills

Data entry

Attention to detail

Time management

Organizational skills

MS Office proficiency

Education

High school diploma or equivalent

Job description

Evolution Research Group seeks a detail-oriented Data Entry Coordinator to manage clinical data entry procedures under the Site Director’s guidance. You will maintain confidential study files, ensure data completeness, and comply with GCP/ICH guidelines and ERG SOPs across studies.

Responsibilities include accurate data entry, quality control, and timely resolution of data queries in collaboration with CRC, Sponsors, or CROs, ensuring high data quality in a fast-paced clinical environment.