Clinical Research Assistant: Data Entry & Patient Recruitment

ObjectiveHealth; South Carolina; Vor Ort; USD 42.000 - 54.000; Vollzeit

Zusammenfassung

ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. The Clinical Research Assistant role focuses on data entry and patient recruitment to support studies and ensure data quality and regulatory compliance.

Ideal candidates have strong people skills, are detail-oriented, and comfortable speaking with potential trial participants by phone. On-site, full-time, with opportunities to grow in clinical research.

Qualifikationen

• High school diploma or equivalent.
• 1+ years of data entry or related experience.
• Research experience or patient recruitment experience is a plus.
• Basic understanding of medical terminology.
• Experience with EMR/healthcare systems.
• Excellent attention to detail and data accuracy.
• Strong written and verbal communication skills.

Aufgaben

• Enter clinical trial data into EDC systems accurately and within required timelines.
• Review source documents to ensure transcription accuracy.
• Verify data for accuracy, completeness, and consistency before submission.
• Resolve data queries from sponsors/CROs by comparing source documentation with study data.
• Communicate with study staff to resolve missing or inconsistent data.
• Maintain audit trails and ensure confidentiality of participant information.
• Identify and pre-screen potential participants and schedule pre-screening and screening visits.
• Collaborate with site teams to meet enrollment targets.

Kenntnisse

Data entry

Attention to detail

Communication skills

Time management

Organizational skills

Multitasking

Ausbildung

High school diploma or equivalent

Tools

EMR systems

EDC systems

Jobbeschreibung

ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. The Clinical Research Assistant role focuses on data entry and patient recruitment to support studies and ensure data quality and regulatory compliance.

Ideal candidates have strong people skills, are detail-oriented, and comfortable speaking with potential trial participants by phone. On-site, full-time, with opportunities to grow in clinical research.