Clinical Research Data Entry Specialist

ObjectiveHealth; Columbia (SC); On-site; USD 25,000 - 33,000; Part time

Job summary

ObjectiveHealth is seeking a meticulous Clinical Research Data Entry Specialist for a part-time onsite role. You will accurately enter, review, and maintain trial data in EDC systems, supporting data quality and regulatory compliance.

Join a team focused on improving patient outcomes at the point of care. The role requires 1+ year of data entry/administrative experience and a high school diploma, with legal authorization to work in the US.

Qualifications

• 1+ years of data entry or administrative experience.
• Attention to detail and data accuracy required.
• Excellent organizational and time management skills.

Responsibilities

• Enter clinical trial data into EDC systems accurately and on time.
• Review source documents and medical records for complete transcription.
• Verify data for accuracy, completeness, and consistency before submission.
• Resolve data queries by comparing source docs and coordinating with study staff.
• Communicate with CRCs, investigators, and staff to resolve missing or inconsistent data.
• Correct data discrepancies with proper audit trails in EDC.
• Ensure timely data entry and query resolution to meet milestones.
• Maintain study documentation related to data entry activities.
• Adhere to GCP, HIPAA, and regulatory guidelines.
• Assist with quality control reviews and sponsor monitoring visits as needed.
• Maintain confidentiality of participant information.

Skills

Data entry

Attention to detail

Organizational skills

Time management

Written & verbal communication

Education

High school diploma or equivalent

Job description

Description

Clinical Research Data Entry Specialist (Part-Time,Onsite)

The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC systems. This role supports clinical research studies by ensuring data quality, completeness, and compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. This position is ideal for a detail-oriented individual with data entry or administrative experience who is interested in building a career in clinical research.

ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to:

• Increase patient access to research trials within our communities
• Provide physicians with enhanced care options for current patients
• Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the ultimate goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.

Key Responsibilities:

• Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines.
• Review source documents and medical records to ensure complete and accurate transcription of participant data.
• Verify data for accuracy, completeness, and consistency prior to submission.
• Review, investigate, and resolve EDC data queries generated by sponsors, contract research organizations (CROs), or data management teams by comparing source documentation and collaborating with study personnel.
• Communicate with Clinical Research Coordinators, investigators, and other study staff to resolve missing, incomplete, or inconsistent data.
• Correct data discrepancies while maintaining appropriate documentation and audit trails within the EDC system.
• Ensure timely completion of data entry and query resolution to support study milestones and database lock.
• Maintain accurate study documentation related to data entry activities.
• Adhere to study protocols, sponsor requirements, Good Clinical Practice (GCP), HIPAA, and applicable regulatory guidelines.
• Assist with quality control reviews and support sponsor monitoring visits, audits, and regulatory inspections as needed.
• Maintain confidentiality of participant information and research data.

Qualifications:

• High school diploma or equivalent.
• 1+ years of data entry, administrative support, medical office, or related experience.
• Excellent attention to detail and data accuracy.
• Strong organizational and time management skills.
• Ability to manage multiple priorities and meet deadlines in a fast-paced environment.
• Strong written and verbal communication skills.

Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant