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Clinical Data Reviewer Jobs in Georgia (NOW HIRING)

CryoLife

Sr. Clinical Data Manager

Kennesaw, GA · On-site

The Sr. Clinical Data Manager is responsible for data management operations and for the ... review, query generation and resolution, and overall maintenance of study databases to ensure data ...

Deloitte

Clinical Data AMS Sr. Consultant

Atlanta, GA · On-site

Provide operational and functional support for eClinical Elluminate, including data review workflows, listings/reports configuration, and integration touchpoints with upstream/downstream clinical ...

Artivion

Sr. Clinical Data Manager

Kennesaw, GA

The Sr. Clinical Data Manager is responsible for data management operations and for the ... review, query generation and resolution, and overall maintenance of study databases to ensure data ...

Zelis

Clinical Nurse Reviewer

Atlanta, GA · On-site

Support administrative tasks such as data entry, case tracking, and report preparation. * Participate in training sessions and shadow senior reviewers to develop clinical review skills. * Maintain ...

Alcanza

Data Entry Coordinator

Decatur, GA

Managing data entry into computer systems for clinical trials, including entering patient data into eDC and other software * Reviewing patient charts and other medical records to ensure data is ...

Grady-Health-System

TRC Data Analyst

Atlanta, GA · On-site

$70 - $110/hr

Atlanta, GADescriptionResponsible for conducting clinical data collection, management, analysis ... facilitate program review, logic model improvement, grant development, program design and ...

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How much do clinical data reviewer jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical data reviewer in Georgia is $22.16, according to ZipRecruiter salary data. Most workers in this role earn between $12.16 and $30.67 per hour, depending on experience, location, and employer.

What is a clinical data reviewer?

A Clinical Data Reviewer is responsible for ensuring the accuracy, consistency, and integrity of clinical trial data. They review patient data in clinical databases, identify discrepancies, and collaborate with data management and clinical teams to resolve issues. Their role is critical in ensuring that trial data meets regulatory standards and supports reliable study outcomes. Clinical Data Reviewers typically have backgrounds in life sciences, clinical research, or data management.

What are the day-to-day responsibilities of a clinical data reviewer?

As a Clinical Data Reviewer, your daily tasks often include evaluating and verifying clinical trial data for completeness, consistency, and accuracy according to study protocols and regulatory requirements. You'll collaborate closely with data managers, clinical research associates, and biostatisticians to resolve discrepancies and ensure data quality. Reviewing case report forms (CRFs), providing feedback on data queries, and documenting findings are typical activities. This role requires ongoing communication and teamwork to maintain timelines and support the integrity of the clinical trial process.

What are the key skills and qualifications needed to thrive as a clinical data reviewer?

To thrive as a Clinical Data Reviewer, you typically need a background in life sciences, experience with clinical research processes, and a keen eye for detail when reviewing clinical trial data. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and compliance frameworks like Good Clinical Practice (GCP) or CDISC standards is highly valued. Strong analytical thinking, effective communication, and the ability to collaborate across multidisciplinary teams are standout soft skills in this role. These competencies are crucial for ensuring the accuracy, reliability, and regulatory compliance of clinical data, ultimately supporting successful research outcomes.

What are the most commonly searched types of Clinical Data Reviewer jobs in Georgia?

The most popular types of Clinical Data Reviewer jobs in Georgia are:

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For Clinical Data Reviewer jobs in Georgia, the most frequently searched job titles are:

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The top searched job categories for Clinical Data Reviewer jobs in Georgia are:

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Cities in Georgia with the most Clinical Data Reviewer job openings:

Clinical Data Reviewer jobs near you
Infographic showing various Clinical Data Reviewer job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $46,089 per year, or $22.2 per hour.

Sr. Clinical Data Manager

CryoLife

Kennesaw, GA • On-site

Full-time

Re-posted 15 days ago

Job description

Company Overview:
Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in treating patients with aortic diseases. Artivion's four major groups of products include: aortic stent grafts, surgical sealants, On-X mechanical heart valves, and implantable cardiac and vascular human tissues. Artivion has over 1,600 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website, www.artivion.com.
Position Overview:
The Sr. Clinical Data Manager is responsible for data management operations and for the organization, coordination and execution of data management activities for assigned studies and projects. This includes but is not limited to database set-up (build, develop, and perform user acceptance testing), development of study documents, training, data review, query generation and resolution, and overall maintenance of study databases to ensure data integrity from study start-up to database lock. This also includes data support for department projects, and inquiries, unrelated to clinical studies.
Responsibilities:
  • Lead, manage, execute end-to-end data management activities for clinical trials conducted inhouse or outsourced to CRO's.
  • Develop and maintain Data Management Plans (DMPs), CRFs, edit check specifications, and other essential documents.
  • Oversee database build.
  • Testing, validation, and UAT processes in EDC systems
  • Ensure timely and high-quality data collection, cleaning, reconciliation, and database lock activities.
  • Collaborate cross-functionally with Clinical Operations, Biostatistics, Regulatory Affairs, QA, and external CROs/vendors.
  • Ensure data integrity and compliance with GCP, FDA, MDR/IVDR, and other applicable regulatory standards.
  • Participate in and contribute to protocol development, case report form design, and data flow diagrams.
  • Conduct and oversee data reconciliation, external data integrations (labs, imaging, etc.), and coding of medical terms (MedDRA, WHO-DD).
  • Provide study specific reports and data listings on regular basis and for ad-hoc requests
  • Support audit readiness and participate in regulatory inspections when required.
  • Mentor junior team members and provide strategic input into department process improvements and SOP development.

Qualifications:
Required:
  • Bachelor's or Master's degree in Life Sciences, Data Science, Computer Science, or a related field.
  • 7+ years of clinical data management experience, with at least 2 years in a senior or lead role.
  • Experience with medical device trials or combination products (IDE, PMA, 510(k), CE marking, etc.).
  • Strong understanding of EDC systems and data standards (CDASH, SDTM, CDISC).
  • Knowledge of regulatory requirements (FDA, EMA, ISO 14155, GCP, GDPR).
  • Excellent organizational, leadership, and communication skills.

Preferred:
  • Experience working in an FDA-regulated and/or ISO-certified environment.
  • Advanced proficiency in data visualization tools and data analytics platforms (such as Python and/or R) is a plus.

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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