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Clinical Data Management Jobs in Georgia (NOW HIRING)

Artivion

Sr. Clinical Data Manager

Kennesaw, GA · On-site

The Sr. Clinical Data Manager is responsible for data management operations and for the ... Develop and maintain Data Management Plans (DMPs), CRFs, edit check specifications, and other ...

CryoLife

Sr. Clinical Data Manager

Kennesaw, GA · On-site

The Sr. Clinical Data Manager is responsible for data management operations and for the ... Develop and maintain Data Management Plans (DMPs), CRFs, edit check specifications, and other ...

Trella Health

Translate clinical and claims data into actionable analytics, including transitions of care ... product management experience in B2B SaaS, with direct ownership of roadmap and product outcomes

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How much do clinical data management jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical data management in Georgia is $48.27, according to ZipRecruiter salary data. Most workers in this role earn between $38.17 and $57.45 per hour, depending on experience, location, and employer.

What is clinical data management?

Clinical data management (CDM) is a critical process in clinical research that involves collecting, cleaning, and managing data generated during clinical trials. The goal is to ensure that the data is accurate, reliable, and compliant with regulatory standards. CDM professionals work closely with researchers, statisticians, and regulatory bodies to validate data and ensure its integrity throughout the study. This process helps in making informed decisions about the safety and efficacy of new drugs or treatments.

What are the key skills and qualifications needed to thrive in clinical data management?

To thrive in Clinical Data Management, you need a strong background in life sciences, attention to detail, and understanding of clinical trial processes, often supported by a relevant degree. Familiarity with industry-standard data management systems such as Medidata Rave or Oracle Clinical, as well as knowledge of CDISC standards and regulatory requirements, is essential. Excellent organizational skills, communication, and problem-solving abilities help ensure data integrity and effective cross-functional collaboration. These skills and qualities are crucial for ensuring high-quality, compliant data that supports clinical research and regulatory submissions.

What are some common challenges faced by professionals in clinical data management, and how can they be addressed?

One of the common challenges in Clinical Data Management is ensuring data accuracy and consistency across multiple sources and formats. This often involves resolving discrepancies and managing large volumes of data within tight timelines. Effective communication with clinical research associates, statisticians, and IT teams is crucial to address data queries promptly and maintain data integrity. Staying updated with regulatory requirements and leveraging advanced data management systems can also help mitigate these challenges and improve overall workflow efficiency.

What is the difference between Clinical Data Management vs Clinical Data Coordinator?

AspectClinical Data ManagementClinical Data Coordinator
ResponsibilitiesDesigning data collection processes, database setup, data validation, and ensuring data quality for clinical trials.Collecting, reviewing, and entering clinical trial data, ensuring accuracy and completeness.
Required SkillsKnowledge of data management systems, clinical trial processes, and data validation techniques.Attention to detail, data entry skills, familiarity with clinical trial documentation.
Work EnvironmentTypically in clinical research organizations, pharmaceutical companies, or CROs.Often within clinical sites or research teams supporting data collection activities.

While both roles focus on clinical trial data, Clinical Data Management involves designing and overseeing data systems and ensuring data integrity, whereas Clinical Data Coordinators handle the day-to-day data collection and entry tasks. Both are essential for successful clinical research but differ in scope and responsibilities.

How do I become a clinical data management?

To become a clinical data manager, typically a bachelor's degree in life sciences, healthcare, or related fields is required. Gaining experience with clinical trial processes, data management tools like EDC systems, and obtaining certifications such as the Society for Clinical Data Management (SCDM) certification can enhance job prospects.

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

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

What are popular job titles related to Clinical Data Management jobs in Georgia?

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

What job categories do people searching Clinical Data Management jobs in Georgia look for?

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

What cities in Georgia are hiring for Clinical Data Management jobs?

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

Clinical Data Management jobs near you
Infographic showing various Clinical Data Management job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 13% Part Time, 7% Contract, and 3% Nights. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $100,404 per year, or $48.3 per hour.

Sr. Clinical Data Manager

Artivion

Kennesaw, GA • On-site

Full-time

Re-posted 21 hours ago

Artivion rating

8.7

Company rating: 8.7 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

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.

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