- Penn Medicine (Bala Cynwyd, PA)
- …shape our future each day. Are you living your life's work? Summary: + The Clinical Documentation Review Specialist is responsible for collaborating with ... appropriate quality patient care and positive patient outcomes. Responsibilities: + Documentation Improvement: Reviews clinical documentation for compliance… more
- Merck (West Point, PA)
- … supply chain deliverables and prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders. + Works directly ... Product and Clinical Finished Goods). + Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as… more
- Penn Medicine (Bala Cynwyd, PA)
- …implements regulatory standards and processes, including improving and maintaining regulatory clinical documentation standards. The Specialist will ... facilitate survey readiness and monitor for ongoing clinical documentation compliance. The Specialist ...develop plans for sustaining the improvements and compliance. The Specialist coordinates documentation review for… more
- Globus Medical, Inc. (Audubon, PA)
- …of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and ... their lives as quickly as possible. **Position Summary:** The Regulatory Affairs Specialist drafts, submits and gains clearance for 510(k) submissions, and approval… more
- West Pharmaceutical Services (Exton, PA)
- …, regulations, technical standards, guidance documents, test reports, clinical /medical terminology, technical product information, and complex documents. + ... Sr. Specialist , Regulatory Project Management (Evergreen Posting) Requisition ID:...regulatory affairs (RA) team's priorities. + Manage the preparation, review , and submission of complex global regulatory filings, information… more
- Catalent Pharma Solutions (Malvern, PA)
- **Enterprise Data Integrations Specialist ** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical ... Delivery (OSD) business unit. On site we have our state-of-the-art laboratory, clinical , and commercial manufacturing plant for oral dose forms in addition to… more
- Insight Global (Malvern, PA)
- …One of our large pharmaceutical clients is looking to hire a Sr Quality Specialist to join the EQ team. The individual will provide QA support for TAR-200 ... the specific tasks required on a daily basis by the position are: Support, review /pre- review , and/or approve the following - -Batch record review -Quarantine… more
- Globus Medical, Inc. (Audubon, PA)
- …of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and ... their lives as quickly as possible. **Position Summary** **:** The Quality Assurance Specialist (QAS) will work within the Quality Assurance department to provide … more
- Globus Medical, Inc. (Audubon, PA)
- …of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and ... annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking and… more
- Elevance Health (Wilmington, DE)
- …Health Information Technician (RHIT), Registered Health Information Administrator (RHIA), Certified Clinical Documentation Specialist (CCDS), Certified ... is responsible for auditing inpatient medical records to ensure clinical documentation supports the conditions and DRGs...the conditions and DRGs billed and reimbursed. Specializes in review of Diagnosis Related Group (DRG) paid claims. **How… more
- University of Pennsylvania (Philadelphia, PA)
- …University of Pennsylvania is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and treatment of cancer. The ACC ... Clinical Research Unit (CRU) is instrumental in the development...working closely with the CRU Regulatory coordinators to manage, review and initiate trials to ensure competitive activation and… more
- Elevance Health (Wilmington, DE)
- …for all lines of business, and its clients. Also responsible for performing clinical reviews of medical records and other documentation to evaluate issues ... of coding and DRG assignment accuracy. Specializes in review of DRG coding via medical record and attending...and audits claims by integrating medical chart coding principles, clinical guidelines and objectivity in the performance of medical… more