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

Artivion

Sr. Clinical Data Manager

Kennesaw, GA

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 ...

IQVIA

Lead Clinical Data Manager (Remote)

Atlanta, GA · Remote

$68K - $217K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for ...

IQVIA

Lead Clinical Data Manager (Remote)

Atlanta, GA · Remote

$68K - $217K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for ...

CryoLife

Sr. Clinical Data Manager

Kennesaw, GA · On-site

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 ...

Milliman

Strategic Data Partnership Manager

Atlanta, GA · Remote

Manage relationships with current data and technology partners -- ensuring they remain productive ... Assess gaps in our data offerings (SDoH, clinical depth, novel real-world sources, etc.), evaluate ...

Mirus LLC

Clinical Specialist

Marietta, GA · On-site

You are the TAVR expert in interpreting clinical data relating to the treatment options for specific patients. • OR/Cath Lab management: In the Cath lab/OR, you provide support during the procedure ...

Mirus LLC

Clinical Specialist

Marietta, GA · On-site

You are the TAVR expert in interpreting clinical data relating to the treatment options for specific patients. • OR/Cath Lab management: In the Cath lab/OR, you provide support during the procedure ...

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All JobsClinical Data Manager JobsClinical Data Manager Jobs in Decatur, GA

Clinical Data Manager information

See Decatur, GA salary details

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$55

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How much do clinical data manager jobs pay per hour?

As of Jun 20, 2026, the average hourly pay for clinical data manager in Decatur, GA is $55.81, according to ZipRecruiter salary data. Most workers in this role earn between $44.13 and $66.44 per hour, depending on experience, location, and employer.

What are some common challenges Clinical Data Managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

What jobs pay 2000 a day?

Clinical Data Managers typically do not earn $2,000 a day; such high daily rates are more common in specialized consulting, executive roles, or freelance positions in fields like finance or law. Some highly experienced professionals or contractors in niche areas may reach this level with advanced skills and certifications, but it is uncommon for standard roles. Most high-paying jobs at this level require extensive experience, advanced degrees, or independent consulting arrangements.

What are the key skills and qualifications needed to thrive as a Clinical Data Manager, and why are they important?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What does a Clinical Data Manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

Is CRA an entry-level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, monitoring, or related fields. Entry-level roles in clinical research often include Clinical Trial Assistants or Coordinators, while CRAs often need knowledge of Good Clinical Practice (GCP) and relevant certifications. However, some companies may offer junior CRA roles for candidates with limited experience who demonstrate strong foundational skills.

What Does a Clinical Data Manager Do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

What is a Clinical Data Manager?

A Clinical Data Manager is responsible for designing, managing, and ensuring the accuracy and integrity of data collected during clinical trials. They work with electronic data capture systems, develop data management plans, and collaborate with research teams to ensure compliance with regulatory standards. Strong attention to detail and knowledge of data management tools like SQL or SAS are essential in this role.

What is the role of a Clinical Data Manager?

A Clinical Data Manager is responsible for designing, implementing, and maintaining systems to collect, manage, and ensure the quality of clinical trial data. They oversee data validation, perform data cleaning, and collaborate with study teams to ensure accurate and compliant data collection using tools like electronic data capture (EDC) systems. Their role is essential for the integrity and reliability of clinical trial results.
More about Clinical Data Manager jobs
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Clinical Data Manager jobs near you
Sr. Clinical Data Manager

Sr. Clinical Data Manager

Artivion

Kennesaw, GA

Full-time

Posted 2 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.

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