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Senior Clinical Study Manager 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 ... Provide study specific reports and data listings on regular basis and for ad-hoc requests * Support ...

CryoLife

Sr. Clinical Data Manager

Kennesaw, GA · On-site

The Sr. Clinical Data Manager is responsible for data management operations and for the ... Provide study specific reports and data listings on regular basis and for ad-hoc requests * Support ...

Becton, Dickinson and Company

Summary: The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations ... Study & Site Management * Serve as CRA for assigned complex clinical studies, providing expert ...

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global ... study teams and sites. * Well-versed in clinical trial management. They are rigorous, detail ...

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Senior Clinical Study Manager information

See Georgia salary details

$18.6K

$105.8K

$173.9K

How much do senior clinical study manager jobs pay per year?

As of Sep 6, 2026, the average yearly pay for senior clinical study manager in Georgia is $105,793.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,800.00 and $132,600.00 per year, depending on experience, location, and employer.

What does a senior clinical study manager do?

A Senior Clinical Study Manager oversees the planning, execution, and management of clinical trials to ensure they comply with regulatory standards and meet study objectives. They coordinate with cross-functional teams, manage study timelines and budgets, and ensure data integrity. Additionally, they are responsible for monitoring the progress of trials, resolving issues that arise, and communicating results to stakeholders. Their role is critical for advancing medical research and ensuring that new treatments are safe and effective.

How does a senior clinical study manager typically collaborate with cross-functional teams during a study?

A Senior Clinical Study Manager works closely with cross-functional teams such as data management, regulatory affairs, biostatistics, medical writing, and clinical operations to ensure smooth study execution. They facilitate regular meetings, coordinate timelines, and address challenges that arise across teams, ensuring everyone aligns with study objectives and regulatory standards. This role often requires strong communication and leadership skills to manage dependencies, resolve conflicts, and keep projects on track. Effective collaboration is key to maintaining study quality and meeting project milestones.

What are the key skills and qualifications needed to thrive as a senior clinical study manager, and why are they important?

To thrive as a Senior Clinical Study Manager, you need in-depth knowledge of clinical trial processes, regulatory guidelines (such as GCP and ICH), and a relevant life sciences degree, often complemented by several years of clinical research experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like ACRP or SOCRA are typically required. Strong leadership, organizational, and communication skills help manage cross-functional teams and ensure effective collaboration with stakeholders. These skills are essential for delivering high-quality, compliant studies on time and within budget, ultimately supporting successful drug development.

What are popular job titles related to Senior Clinical Study Manager jobs in Georgia?

For Senior Clinical Study Manager jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Senior Clinical Study Manager jobs in Georgia look for?

The top searched job categories for Senior Clinical Study Manager jobs in Georgia are:

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Senior Clinical Study Manager jobs near you
Infographic showing various Senior Clinical Study Manager job openings in Georgia as of August 2026, with employment types broken down into 80% Full Time, 11% Part Time, 6% Contract, and 3% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $105,793 per year, or $50.9 per hour.

Sr. Clinical Data Manager

Artivion

Kennesaw, GA • On-site

Full-time

Re-posted 20 days 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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