- Actalent (Philadelphia, PA)
- Job Title: Protocol Review and Monitoring Committee Coordinator MUST be within a 2 hour radius of Philadelphia, PA Job Description Coordinate all ... storage capacity. + Serve as a backup for the Protocol Review Committee as needed....for document preparation and communication. + Ability to manage monitoring visits and submissions. + Understanding of medical terminology… more
- J&J Family of Companies (Spring House, PA)
- …conduct of high-quality oncology clinical trials is required. + Experience in protocol development, medical review , oversight of study conduct, running trials, ... Study Responsible Physician will represent the clinical team in governance and committee meetings relating to the overall strategy and operational implementation of… more
- Penn Medicine (Philadelphia, PA)
- …to accurately reflect current status of patient's pending items needed for ongoing review of transplant candidacy per department protocol . + Completes HLA ... reports/studies required to complete the evaluation. They are also responsible for monitoring and maintaining up-to-date information for all patients on the United… more
- Sumitomo Pharma (Harrisburg, PA)
- …and at partner meetings including Joint Safety Forums (JSFs) and Pharmacovigilance Committee (PVC) meetings. + Review adverse event reports-including serious ... Serve as a subject matter expert (SME) in study protocol design, review interim clinical trial reports,...benefit-risk profile of assigned products, ensuring patient safety. + Review literature search strategies and literature monitoring … more
- Bausch + Lomb (Harrisburg, PA)
- …+ Manage and/or oversee the development process for critical study documents (eg, protocol , amendments, IB, ICF, and CRFs). Will also work closely with members of ... clinical study sites including training of site personnel in the study protocol and other study-specific procedures. + Supervise clinical operations team to ensure… more
- ThermoFisher Scientific (Allentown, PA)
- …the latest scientific information, contribute to site selection, contribute to review and approval of study protocols and amendments, Clinical Study Reports ... (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical… more
- Heritage Ministries (Conneautville, PA)
- …and will collect full financial disclosure form - addendum III. If only a partial review is needed, will explain what documents are required to fully open the long ... party's ability to complete the process per the established protocol . Will provide supervision and guidance until the process...payment for services provided during the stay and to review the status of coverage for the stay and… more
- UPMC (Pittsburgh, PA)
- …members.Request assistance in planning and prioritizing activities as needed.Participate in self- review as requested by the director. Participate in project and ... committee work.Complete required education to maintain medic command. +...assistance in planning and prioritizing activities as needed.Participates in self- review as requested by the clinical director. Participates in… more
- Teleflex (Wayne, PA)
- …successfully interact with CROs, CRAs (Clinical Research Associates), IRBs (Institutional Review Boards), EC (Ethical Committee ), and other clinical authorities. ... of building diverse clinical research teams with competencies that include protocol design, site selection, contracting and management, consent and IRB interactions,… more
- WellSpan Health (Chambersburg, PA)
- …resources. 7. Demonstrates involvement in unit by attending 50% of staff/ committee meetings and in-services for area. 8. Demonstrates leadership through the ... 2. Demonstrates correct patient identification by following the universal protocol . 3. Completes preoperative teaching and documents PAT assessment information.… more
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