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HomeCompanies9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001Senior Specialist, Laboratory Compliance Support (CLIA)

Senior Specialist, Laboratory Compliance Support (CLIA)

9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001 · Newark, DE, US, Newark, DE · On Site · Active · $47,000–$53,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001
TitleSenior Specialist, Laboratory Compliance Support (CLIA)
Normalized title-
Department / team-
LocationNewark, DE, United States
Work modelOn Site
Employment typeFull Time
Salary$47,000–$53,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-03-13 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from 9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Newark.Open
Work model jobsActive On Site postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

Company9ee3716b B93b 41d4 B702 C8728d7396d2 19000101 000001
Source23fd82d9-c7cc-4299-8499-ec8ee9834434
ATS providerADP Workforce Now Recruiting

Description

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS’s Story QPS Holdings, LLC is a global, full-service contract research organization (CRO) providing discovery, preclinical, bioanalytical, and clinical research services to pharmaceutical and biotechnology clients worldwide. Founded in 1995, QPS has grown into an award-winning CRO supporting drug development programs across the globe. Our teams work collaboratively to deliver high-quality data that helps advance new therapies. The Job The Senior Specialist, Laboratory Compliance Support (CLIA) provides documentation management, record maintenance, and administrative support for CLIA-regulated laboratory activities within the Translational Medicine department. This role works closely with and supports the Senior Research Fellow in maintaining CLIA compliance by ensuring that regulatory documentation, personnel records, and quality system materials are accurate, complete, and inspection ready. The position also supports operational activities related to CLIA testing for clinical trials and internal projects. This is an individual contributor role focused on documentation management, compliance tracking, and laboratory administrative coordination in a regulated environment - ideal for someone who enjoys organizing complex documentation and maintaining detailed records in a regulated environment. You’ll gain hands-on exposure to CLIA compliance, laboratory quality systems, and clinical trial testing while helping keep our laboratory organized, compliant, and inspection-ready in support of research advancing new medicines and therapies. Key Responsibilities Maintain CLIA personnel files and regulatory documentation, ensuring records are current, complete, and well organized Support the Senior Research Fellow in maintaining CLIA compliance documentation and tracking regulatory requirements Assist with renewals and documentation related to CLIA permits, licenses, and laboratory test menus Maintain organized filing systems for compliance documentation, quality records, and IVD tracking materials Support quality system activities, including documentation coordination, QC data tracking, and preparation of reports Assist with administrative aspects of CLIA testing, including maintaining test recipient lists, generating reports, and performing data quality checks Track and coordinate responses to internal and client inquiries related to test data and documentation Support training documentation, continuing education tracking, and other compliance-related recordkeeping Collaborate with internal teams to ensure documentation is accurate, accessible, and audit-ready Work Location This is a fully onsite role based at our QPS facility in Newark, DE. Requirements Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbent’s success in this role, such as: University/College Degree in relevant Scientific discipline, and/or Demonstrated experience in CRO, Clinical Research, or another relevant field. Experience in a CRO, clinical research organization, regulated laboratory, or similar life sciences environment preferred Experience supporting regulatory documentation, quality systems, or laboratory compliance activities is a plus Why You Should Apply Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals, with structured Career Ladders that provide excellent growth based on your personal aspirations Total rewards package that includes bonuses and merit increases linked to individual, team and company performance. We also offer a solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance Park-like setting in Newark, Delaware Internal committees designed with the needs and enjoyment of QPS employees in mind. QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Full job record

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Org ID0f4148ca-92b4-4d63-a472-f1eb4a8db51c
Source ID23fd82d9-c7cc-4299-8499-ec8ee9834434
Board ID23fd82d9-c7cc-4299-8499-ec8ee9834434
Provideradp_workforcenow
Provider Job Key588268
TitleSenior Specialist, Laboratory Compliance Support (CLIA)
Normalized Title
Statusactive
Activeyes
Location TextNewark, DE, US, Newark, DE
Department
Team
Employment Typefull_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionDE
CityNewark
Salary Raw47000.00 To 53000.00 (USD) Annually
Salary Min47,000
Salary Max53,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=9ee3716b-b93b-41d4-b702-c8728d7396d2&ccId=19000101_000001&lang=en_US&type=JS&jobId=588268&jwId=9201166644169_1
Apply URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=9ee3716b-b93b-41d4-b702-c8728d7396d2&ccId=19000101_000001&lang=en_US&type=JS&jobId=588268&jwId=9201166644169_1
First Seen At2026-05-31 18:25:14Z
Last Seen At2026-06-06 13:18:39Z
Last Checked At2026-06-06 13:18:39Z
Last Changed At2026-06-06 13:18:39Z
Inactive At
Source Posted At2026-03-13 18:47:00Z
Source Updated At
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    "requisitionDescription": "<div><div><div><div><div><div><div><div><div><div><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;' data-pasted=\"true\"><strong><span style=\"font-family: verdana, sans-serif; font-size: 14px;\">Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!&nbsp;</span></strong></p><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;'><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><br></span></p><p style=\"margin: 0in; font-size: 16px; font-family: Aptos, sans-serif; line-height: 1.5;\" data-pasted=\"true\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong>QPS&rsquo;s Story</strong></span></p><p style=\"margin: 0in; font-size: 16px; font-family: Aptos, sans-serif;\"><span style=\"font-size: 14px; font-family: verdana, sans-serif;\">QPS Holdings, LLC is a global, full-service contract research organization (CRO) providing discovery, preclinical, bioanalytical, and clinical research services to pharmaceutical and biotechnology clients worldwide. Founded in 1995, QPS has grown into an award-winning CRO supporting drug development programs across the globe. Our teams work collaboratively to deliver high-quality data that helps advance new therapies.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><br></span></p><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;background:#D9D9D9;' data-pasted=\"true\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong><span style=\"color:black;\">The Job</span></strong></span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><br></span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-size: 14px; font-family: verdana, sans-serif;\">The <strong>Senior Specialist, Laboratory Compliance Support (CLIA)</strong> provides documentation management, record maintenance, and administrative support for CLIA-regulated laboratory activities within the Translational Medicine department. This role works closely with and supports the Senior Research Fellow in maintaining CLIA compliance by ensuring that regulatory documentation, personnel records, and quality system materials are accurate, complete, and inspection ready. The position also supports operational activities related to CLIA testing for clinical trials and internal projects.</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><br></span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-size: 14px; font-family: verdana, sans-serif;\">This is an individual contributor role focused on documentation management, compliance tracking, and laboratory administrative coordination in a regulated environment - ideal for someone who enjoys organizing complex documentation and maintaining detailed records in a regulated environment. You&rsquo;ll gain hands-on exposure to CLIA compliance, laboratory quality systems, and clinical trial testing while helping keep our laboratory organized, compliant, and inspection-ready in support of research advancing new medicines and therapies.&nbsp;</span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><br></span></p><p style='margin:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong>Key Responsibilities</strong></span></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Maintain CLIA personnel files and regulatory documentation, ensuring records are current, complete, and well organized&nbsp;</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Support the Senior Research Fellow in maintaining CLIA compliance documentation and tracking regulatory requirements&nbsp;</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Assist with renewals and documentation related to CLIA permits, licenses, and laboratory test menus&nbsp;</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Maintain organized filing systems for compliance documentation, quality records, and IVD tracking materials&nbsp;</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Support quality system activities, including documentation coordination, QC data tracking, and preparation of reports&nbsp;</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Assist with administrative aspects of CLIA testing, including maintaining test recipient lists, generating reports, and performing data quality checks&nbsp;</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Track and coordinate responses to internal and client inquiries related to test data and documentation&nbsp;</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Support training documentation, continuing education tracking, and other compliance-related recordkeeping&nbsp;</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Collaborate with internal teams to ensure documentation is accurate, accessible, and audit-ready&nbsp;</li></ul><p style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><br></span></p><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;background:#D9D9D9;' data-pasted=\"true\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong><span style=\"color:black;\">Work Location</span></strong></span></p><ul type=\"disc\"><li style=\"font-size: 14px; font-family: verdana, sans-serif;\">This is a <strong>fully</strong><strong>&nbsp;onsite&nbsp;</strong>role based at our QPS facility in Newark, DE.</li></ul><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;background:#D9D9D9;' data-pasted=\"true\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong><span style=\"color:black;\">Requirements</span></strong></span></p><ul style=\"list-style-type: disc;margin-left: 0.09999999999999964px;\"><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Combination of relevant education &amp; experience that provides sufficient knowledge &amp; skills to ensure incumbent&rsquo;s success in this role, such as:&nbsp;<ul style=\"list-style-type: circle; font-family: initial; font-size: initial;\"><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">University/College Degree in relevant Scientific discipline, and/or&nbsp;</li><li style=\"font-family: verdana, sans-serif; font-size: 14px;\">Demonstrated experience in CRO, Clinical Research, or another relevant field.&nbsp;</li></ul></li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\" data-pasted=\"true\">Experience in a CRO, clinical research organization, regulated laboratory, or similar life sciences environment preferred&nbsp;</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Experience supporting regulatory documentation, quality systems, or laboratory compliance activities is a plus&nbsp;</li></ul><p style='margin:0in;font-size:15px;font-family:\"Arial\",sans-serif;background:#D9D9D9;' data-pasted=\"true\"><span style=\"font-family: verdana, sans-serif; font-size: 14px;\"><strong><span style=\"color:black;\">Why You Should Apply</span></strong></span></p><ul type=\"disc\"><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\" data-pasted=\"true\">Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals, with structured Career Ladders that provide excellent growth based on your personal aspirations</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Total rewards package that includes bonuses and merit increases linked to individual, team and company performance. We also offer a solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&amp;D and Short and Long-term Disability Insurance</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Park-like setting in Newark, Delaware</li><li style=\"margin: 0in; font-size: 14px; font-family: verdana, sans-serif;\">Internal committees designed with the needs and enjoyment of QPS employees in mind.&nbsp;</li></ul><p><span style=\"font-size: 14px; font-family: verdana, sans-serif;\">QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. &nbsp;In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.&nbsp;</span></p></div></div></div></div></div></div></div></div></div></div>\n",
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Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/93aa6cb72169141e07df34abe51d227ceadd7ec6?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/0f4148ca-92b4-4d63-a472-f1eb4a8db51cJSON
GET https://api.bluedoor.sh/job-postings/v1/sources/23fd82d9-c7cc-4299-8499-ec8ee9834434JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/93aa6cb72169141e07df34abe51d227ceadd7ec6/eventsJSON