- 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
- Penn Medicine (Philadelphia, PA)
- …Our employees shape our future each day. Are you living your life's work? **HIM Clinical Documentation Specialist ** Job Summary: + The Clinical ... care teams and the Corporate HIM teams, the Clinical Documentation Specialist will educate...Improvement to develop/upkeep efficiencies/synergies within the Clinical Documentation department + Enter clinical review… more
- University of Pennsylvania (Philadelphia, PA)
- …health and wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile Title ... Clinical Research Regulatory Specialist B Job Description Summary The Abramson Cancer Center...Reporting to the Regulatory Affairs New Study & Continuing Review Manager, the Regulatory Affairs Start-Up Specialist -CC… more
- Sevita (Philadelphia, PA)
- …adults with intellectual and developmental disabilities and medically complex conditions. ** Clinical Specialist (Behavior Specialist )** **Hours: 9a-5p M-F** ... a team-based workplace that puts people first. As the Clinical Specialist , you will provide services in...appropriate settings such as home, school, or community. + Review social history information, complete functional assessments, and target… 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
- Penn Medicine (Philadelphia, PA)
- …lab services in support of special projects and research protocols; Meets with clinical research sponsors/auditors to review lab service support for various ... ancillary tasks required to operate the laboratory. **Credentials:** + Appropriate specialist certification from ASCP (American Society for Clinical Pathology)… more
- Merck (North Wales, PA)
- … Trials Regulation of the European Union). + Responding to internal and clinical review comments on public disclosures; amending disclosures as appropriate and ... & Disclosure Department of the GCTO organization prepares a variety of regulated documentation in support of the clinical development portfolio and compliance in… more
- University of Pennsylvania (Philadelphia, PA)
- …Regulatory Affairs Veeva Quality Assurance Specialist to participate in the review and migration of Phase I-V clinical trial investigator site files ... and much more. Posted Job Title Veeva Quality Assurance Specialist (Abramson Cancer Center) Job Profile Title Clinical...Lead, the Veeva Quality Assurance Specialist will review , itemize and migrate all regulatory documentation … more
- The Cigna Group (Philadelphia, PA)
- **Coding Education Specialist (AHIMA or AAPC certified) -** **Philadelphia, PA or Nashville TN** We value our talented employees, and whenever possible strive to ... Professional Coder (CPC) Certified Risk Adjustment Coder (CRC) Certified Coding Specialist for Providers (CCS-P) Certified Coding Specialist for Hospitals… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Regulatory Affairs Specialist C Job Profile Title Clinical Research Regulatory Specialist ... reviewing entities. Ensure high quality of the research projects assigned and documentation is current and complete. Review relevant safety information, obtain… more
- University of Pennsylvania (Philadelphia, PA)
- …Job Profile Title Research Coordinator Senior Job Description Summary The Quality Assurance Specialist will work within the Clinical Cell and Vaccine Production ... clinical trials in immunotherapies. Main duties include: + Review of manufacturing batch records and product release ...Review of manufacturing batch records and product release documentation under tight deadlines with impact on patients and… 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
- Penn Medicine (Philadelphia, PA)
- …Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn ... our future each day. Are you living your life's work? **Entity** : Clinical Practices of the University of Pennsylvania (CPUP) **Department** : Ophth Clinical… more
- Penn Medicine (Philadelphia, PA)
- …a Coding Quality Specialist to query the physician for the needed documentation . + Promptly and accurately assigns Coding Hold reasons to all records that cannot ... Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn… more
- Penn Medicine (Philadelphia, PA)
- …Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn ... our future each day. Are you living your life's work? Entity: Clinical Practices of the University of Pennsylvania (CPUP) Department: Dermatology Location: Centre… more
- Penn Medicine (Philadelphia, PA)
- …a Coding Quality Specialist to query the physician for the needed documentation . + Promptly and accurately assigns Coding Hold reasons to all records that cannot ... Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn… 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