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Clinical Records Associate
Integratedresourcesinc · Foster, CA, United States · Active · SmartRecruiters
Job facts
| Field | Value |
|---|---|
| Company | Integratedresourcesinc |
| Title | Clinical Records Associate |
| Normalized title | - |
| Department / team | Research |
| Location | Foster, CA, United States |
| Work model | - |
| Employment type | Contract |
| Salary | - |
| Status | active |
| ATS provider | SmartRecruiters |
| Posted / first seen | 2017-08-24 / 2026-05-31 |
| Changed / last seen | 2026-05-31 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Integratedresourcesinc. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through SmartRecruiters. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Foster. | Open |
| Department jobs | Active postings in Research. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Integratedresourcesinc |
| Source | ae034262-ce37-4bac-8f9f-2cc70071dd78 |
| ATS provider | SmartRecruiters |
Description
Job Description:
* Maintain a minimal understanding of GCP, ICH and GLP regulations associated with the maintenance and retention of clinical trial documentation and preclinical study records.
* Participate in continued security and maintenance of the Trial Master File (TMF) Room.
* Participate in offsite storage activates.
* Create and maintain study specific file structures for Gilead clinical, biometrics, and preclinical documents and file documents accordingly.
* Ensure record filing is kept up to date and is performed accurately.
* Perform an inventory review for incoming CRO clinical study files; receive, index, and file preclinical study records; responsible for offsite archival of documents; participate in periodic file room utilization reviews; file incoming documents and retrieve documentation from the TMFR upon request.
* May provide support during TMF-related regulatory agency and internal GCP inspections readiness.
* Assist in the development of electronic tracking/ filing systems
Rupalim Dutta
Clinical Recruiter
Integrated Resources , Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE | GSA - Schedule 66 I GSA - Schedule 621I
DIRECT # 650-399-0896
LinkedIn: www.linkedin.com/in/rupalim-dutta
Full job record
| Job ID | 8339cb7e9f2eb487c709fa56985781d1719c5ad1 |
| Org ID | 79218e32-f5f6-41f2-9180-6b2e3efeeaa3 |
| Source ID | ae034262-ce37-4bac-8f9f-2cc70071dd78 |
| Board ID | ae034262-ce37-4bac-8f9f-2cc70071dd78 |
| Provider | smartrecruiters |
| Provider Job Key | 743999658581488 |
| Title | Clinical Records Associate |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Foster, CA, United States |
| Department | Research |
| Team | — |
| Employment Type | contract |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | CA |
| City | Foster |
| Salary Raw | Job Description: * Maintain a minimal understanding of GCP, ICH and GLP regulations associated with the maintenance and retention of clinical trial documentation and preclinical study records. * Participate in continued security and maintenance of the Trial Master File (TMF) Room. * Participate in offsite storage activates. * Create and maintain study specific file structures for Gilead clinical, biometrics, and preclinical documents and file documents accordingly. * Ensure record filing is kept up to date and is performed accurately. * Perform an inventory review for incoming CRO clinical study files; receive, index, and file preclinical study records; responsible for offsite archival of documents; participate in periodic file room utilization reviews; file incoming documents and retrieve documentation from the TMFR upon request. * May provide support during TMF-related regulatory agency and internal GCP inspections readiness. * Assist in the development of electronic tracking/ filing systems Rupalim Dutta Clinical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO Certified MBE | GSA - Schedule 66 I GSA - Schedule 621I DIRECT # 650-399-0896 LinkedIn: www.linkedin.com/in/rupalim-dutta |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://jobs.smartrecruiters.com/IntegratedResourcesINC/743999658581488-clinical-records-associate |
| Apply URL | https://jobs.smartrecruiters.com/IntegratedResourcesINC/743999658581488-clinical-records-associate?oga=true |
| First Seen At | 2026-05-31 17:47:57Z |
| Last Seen At | 2026-06-06 10:48:54Z |
| Last Checked At | 2026-06-06 10:48:54Z |
| Last Changed At | 2026-05-31 17:47:57Z |
| Inactive At | — |
| Source Posted At | 2017-08-24 23:46:29Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=smartrecruiters/board=integratedresourcesinc/date=2026-06-06/2026-06-06T10-48-17-956Z-091e2bdb24fc8ae6fddb178aae9a9aac35c5d8b3b52c6414b9a333424f393043.json |
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