Clinical Data Entry Specialist

IQVIA; San Antonio (TX); Vor Ort; USD 26.000 - 65.000; Vollzeit

Zusammenfassung

IQVIA is seeking a Data Entry Specialist to support clinical studies under the Director of Data Management. You will enter study data into the EDC system, ensure accuracy, and resolve data queries in collaboration with research coordinators.

Responsibilities include overseeing data entry from source documents to CRFs, reviewing patient records for completeness, and coordinating with sponsors and monitors. Familiarity with SOPs and regulatory guidelines is essential.

Qualifikationen

• High School Diploma is required.
• Associate degree or certificate program is preferred.
• Working knowledge of clinical research Electronic Data Capture (EDC) systems.
• Knowledge of ICH GCP, FDA, OHRP, OSHA and HIPAA guidelines pertaining to clinical research

Aufgaben

• Oversee data entry from source documents to the CRF.
• Reviews patient records for completeness and accuracy.
• Meets with sponsor/monitors to review data entry.
• Serves as a backup to help coordinate and schedule monitoring visits.
• Serves as a backup to provide support and information to monitors as necessary and as directed by supervisor(s).
• Timely resolution of data queries promptly to insure completeness of CRFs.
• Assures that data entry remains current for all studies per SOP.
• Complies with all applicable regulations, guidelines and procedures pertaining to dataloading, EDC and clinical research.

Kenntnisse

EDC systems

Interpersonal skills

Medical terminology

ICH GCP knowledge

Organizational skills

Prioritization

Multi-tasking

Team player

Communication skills

Ausbildung

High School Diploma

Associate degree or certificate

Jobbeschreibung

IQVIA is seeking a Data Entry Specialist to support clinical studies under the Director of Data Management. You will enter study data into the EDC system, ensure accuracy, and resolve data queries in collaboration with research coordinators.

Responsibilities include overseeing data entry from source documents to CRFs, reviewing patient records for completeness, and coordinating with sponsors and monitors. Familiarity with SOPs and regulatory guidelines is essential.