- Olympus Corporation of the Americas (Center Valley, PA)
- …more about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr. Clinical Trial Coordinator (Sr. CTC) will be responsible for ... and primary point of accountability and reconciliation for the Trial Master File (TMF) and the Investigator Site...resolution of data queries under the guidance of the Clinical Research Associate (CRA), Data Management and/or… more
- Sumitomo Pharma (Harrisburg, PA)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- IQVIA (Philadelphia, PA)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures...activities from start-up to close-out. + Escalate and resolve trial issues and contribute to CAPA processes. ** Site… more
- IQVIA (Philadelphia, PA)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... inspection readiness, and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is… more
- Parexel (Harrisburg, PA)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible for the site...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- ICON Clinical Research (Blue Bell, PA)
- …a Senior Clinical Research Associate . + In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. + Strong organizational and ... Clinical Research Associate or Senior ...protocol compliance, data integrity, and patient safety throughout the trial process. + Collaborating with investigators and site… more
- ICON Clinical Research (Blue Bell, PA)
- …CRA II consideration and 3 years for Senior CRA. + Strong knowledge of clinical trial processes, regulatory requirements, and ICH-GCP guidelines, with a genuine ... development. ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or ...protocol compliance, data integrity, and patient safety throughout the trial process. + Collaborating with investigators and site… more
- ICON Clinical Research (PA)
- Senior Clinical Supply Associate - 12 pm...Doing:** + Managing the planning, coordination, and execution of clinical trial supplies to ensure timely and ... clinical development. We are currently seeking a Senior Clinical Supply Associate to join our diverse... supply chain management, with a deep understanding of clinical trial processes and regulatory standards. +… more
- Sumitomo Pharma (Harrisburg, PA)
- …clinical research program with minimal direction + Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing ... a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The medical… more
- ICON Clinical Research (Blue Bell, PA)
- …+ Oversees IP shipment orders according to supply plans or as requested by Clinical Trial Management team, to ensure timely and compliant shipment and delivery ... to investigator sites. Works with Clinical Logistics Associate to complete this activity...evaluates temperature excursion data and communicates stability information to clinical trial managers, CROs, and investigator sites;… more