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Clinical Data Entry Jobs in Decatur, GA (NOW HIRING)

CenExel

Data Entry Coordinator

Atlanta, GA · On-site

CenExel is a leading nationwide clinical research site and patient network serving the life ... Under moderate supervision, the Data Entry Coordinator I transcribes clinical research data ...

IQVIA

Clinical Research Coordinator

Marietta, GA

$35 - $42/hr

Clinical Research Coordinator - Marietta, GA Work Set-Up: On-site Schedule Weekly Hours: 24 hours ... Proficiency with EDC systems , data entry accuracy, and query management. Please note: This ...

Key2Source Inc

Database Administrator 1

Atlanta, GA · On-site

$30 - $40/hr

Run SQL queries and reports to validate and correct front desk and clinical data . * Perform ... for data entry and reporting. * Support cleanup of duplicate patient records to ensure EHR ...

Apidel Technologies

Database Administrator 1

Decatur, GA · On-site

... entry errors. Perform routine audits for the following: Benefit Assignments: End-date outdated or ... Clinical Data Integrity Analyze service records for completeness, accuracy, and compliance with ...

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Clinical Data Entry information

See Decatur, GA salary details

$13

$38

$84

How much do clinical data entry jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for clinical data entry in Decatur, GA is $38.03, according to ZipRecruiter salary data. Most workers in this role earn between $28.65 and $38.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in clinical data entry, and why are they important?

To thrive as a Clinical Data Entry professional, you need excellent attention to detail, strong organizational skills, and a solid understanding of medical terminology, often supported by a high school diploma or associate’s degree. Familiarity with electronic data capture (EDC) systems, clinical databases, and sometimes certifications like Certified Clinical Data Manager (CCDM) is highly valuable. Strong communication, time management, and the ability to maintain confidentiality make someone stand out in this role. These skills ensure accurate data capture, regulatory compliance, and efficient support of clinical research processes.

What are the typical daily responsibilities of a clinical data entry?

Clinical Data Entry professionals are primarily responsible for accurately entering, updating, and verifying clinical trial or patient data in designated databases or electronic systems. They work closely with clinical research coordinators, data managers, and healthcare staff to ensure all data is complete, consistent, and compliant with regulations. Daily tasks may include resolving data discrepancies, performing quality checks, and managing documentation. Attention to detail and adherence to strict timelines are essential for ensuring the integrity of clinical data.

What is a clinical data entry?

A Clinical Data Entry job involves accurately inputting, updating, and managing clinical and medical data into databases or electronic health records. Professionals in this role ensure data integrity, compliance with regulations, and confidentiality. They may work with patient records, clinical trial data, or research information. Strong attention to detail, familiarity with medical terminology, and proficiency in data management systems are typically required.

How to become a clinical data entry?

To become a clinical data entry specialist, typically, candidates need a high school diploma or equivalent and proficiency in data management software such as Excel or electronic health record systems. Attention to detail, strong organizational skills, and basic knowledge of medical terminology are important; some roles may require certification or training in clinical data management. On-the-job training is common, and familiarity with healthcare environments can be beneficial.
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Clinical Data Entry jobs near you
Infographic showing various Clinical Data Entry job openings in Decatur, GA as of July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 16% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $79,103 per year, or $38 per hour.

Data Entry Coordinator

Atlanta Center for Medical Research

Atlanta, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired today. Applications are no longer accepted.

Job description

About Us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
Under moderate supervision, the Data Entry Coordinator I transcribes clinical research data correctly from source documents to electronic data capture following ALCOA-C principles.
Essential Responsibilities and Duties:
  • Ensures timely data entry thru department and study tracking, etc.
  • Maintains healthy professional relationships with Clinical Operations, Quality, Regulatory, CROs, Sponsors, etc., as well key clinical trial personnel.
  • Transcribes data accurately and efficiently from source documents to electronic data capture.
  • Assists in preparing for internal and external data audits along with the clinical operations/ quality/ and regulatory teams.
  • Completes training and obtains applicable certificates and access to CRFs/EDC.
  • Verifies source documents (e.g., "buddy check").
  • Assists CRCs in entering data from paper source documents to eCRFs correctly, accurately and on a timely manner for multiple clinical trials.
  • Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • Minimum High School graduate or equivalent.
  • One year of data entry or related preferred.
  • Must have excellent computer skills and medical/research terminology.
  • Must be self-directed and able to work with minimal supervision.
  • Motivated to work consistently in a fast paced and rapidly changing environment.
  • Able to manage multiple projects and responsibilities.
  • Must be able to effectively communicate verbally and in writing.

Working Conditions
  1. Indoor, Office environment.
  2. Essential physical requirements include sitting, typing, standing, and walking.
  3. Lightly active position, occasional lifting of up to 20 pounds.
  4. Reporting to work, as scheduled, is essential.
  5. On site work arrangement.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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