Sr. Clinical Data Manager

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, 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. #J-18808-Ljbffr