{"schemaVersion":"jobsearcher.job.v1","id":"232d942487fb06669cc50c53","url":"https://jobsearcher.com/jobs/232d942487fb06669cc50c53","canonicalUrl":"https://jobsearcher.com/jobs/232d942487fb06669cc50c53","title":"Manager, Quality Control & Data Entry","description":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.\n\nResponsible for managing the data workflow through Quality Control (QC) and Data Entry (DE) for studies, maintains timelines for client deliverables and ensures regulatory compliance. Requires interface with other departments and/or sites. Requires interface with Sponsors.\nEssential Functions\nResponsible for staff management in accordance with the organization's policies and applicable laws\nResponsibilities include interviewing, hiring, and training employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems; development and coaching of employees\nCommunicate and provide support/guidance to appropriate groups/staff as required to ensure established, revised and/or new processes are followed to ensure quality on-time/zero defect standards\nPlan, organize and facilitate workloads and schedules of staff to ensure that timelines are met and are compliant with regulatory and internal procedure requirements.\nAttend and participate in study specific meetings related to study set up, timeline production and management, and study status\nMay be required to carry out study tasks, including but not limited to, complete QC review of source data and raw data for studies, performing accurate data entry, attending internal study initiation meetings to determine QC criteria and timelines for studies\nWrite QC and DE SOPs and Procedure guides and participate in SOP and Procedure Guide Reviews\nCreate and track metrics associated with QC and DE responsibilities\nPresent the QC processes to sponsors and auditors\nLead Process Improvement initiatives to improve the quality of the source data\nParticipate in regulatory inspections, audits and meet with Sponsors as required\nMonitor process efficiency and implement process improvement as needed, including data flow and identification of error trends and resolutions.\nLead and/or participate in problem solving for the data collection, quality control and data entry processes.\nKnowledge/Skills/Education/Licenses\nBachelor’s degree in a related field is required.\n1-2 years of supervisory or trainer/leader experience required.\nKnowledge of Good Clinical Data Management Practices, Medical Terminology, GCP, ICH Guidelines, and 21 CFR Part11 preferred\nAbility to adjust hours to meet workload priorities\nStrong process improvement skills and change management experience\nCritical thinking skills\nClinical data experience preferred\n**Equivalent education and experience will be consider\nCelerion Values: Integrity Trust Teamwork Respect\n\nAre you ready to join our team?\n\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n\nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n\nWe may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.","company":"Celerion","rawCompany":"celerion","city":"Tempe","state":"AZ","isRemote":false,"isActive":false,"createdAt":"2026-09-02T08:18:46.182Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"},{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Manager, Quality Control & Data Entry","description":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.\n\nResponsible for managing the data workflow through Quality Control (QC) and Data Entry (DE) for studies, maintains timelines for client deliverables and ensures regulatory compliance. Requires interface with other departments and/or sites. Requires interface with Sponsors.\nEssential Functions\nResponsible for staff management in accordance with the organization's policies and applicable laws\nResponsibilities include interviewing, hiring, and training employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems; development and coaching of employees\nCommunicate and provide support/guidance to appropriate groups/staff as required to ensure established, revised and/or new processes are followed to ensure quality on-time/zero defect standards\nPlan, organize and facilitate workloads and schedules of staff to ensure that timelines are met and are compliant with regulatory and internal procedure requirements.\nAttend and participate in study specific meetings related to study set up, timeline production and management, and study status\nMay be required to carry out study tasks, including but not limited to, complete QC review of source data and raw data for studies, performing accurate data entry, attending internal study initiation meetings to determine QC criteria and timelines for studies\nWrite QC and DE SOPs and Procedure guides and participate in SOP and Procedure Guide Reviews\nCreate and track metrics associated with QC and DE responsibilities\nPresent the QC processes to sponsors and auditors\nLead Process Improvement initiatives to improve the quality of the source data\nParticipate in regulatory inspections, audits and meet with Sponsors as required\nMonitor process efficiency and implement process improvement as needed, including data flow and identification of error trends and resolutions.\nLead and/or participate in problem solving for the data collection, quality control and data entry processes.\nKnowledge/Skills/Education/Licenses\nBachelor’s degree in a related field is required.\n1-2 years of supervisory or trainer/leader experience required.\nKnowledge of Good Clinical Data Management Practices, Medical Terminology, GCP, ICH Guidelines, and 21 CFR Part11 preferred\nAbility to adjust hours to meet workload priorities\nStrong process improvement skills and change management experience\nCritical thinking skills\nClinical data experience preferred\n**Equivalent education and experience will be consider\nCelerion Values: Integrity Trust Teamwork Respect\n\nAre you ready to join our team?\n\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n\nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n\nWe may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.","datePosted":"2026-09-02T08:18:46.182Z","dateModified":"2026-09-02T08:18:46.182Z","hiringOrganization":{"@type":"Organization","name":"Celerion","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Tempe","addressRegion":"AZ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"232d942487fb06669cc50c53"},"url":"https://jobsearcher.com/jobs/232d942487fb06669cc50c53"}}