- 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
- Parexel (Harrisburg, PA)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring… more
- ICON Clinical Research (PA)
- …a Clinical Research Associate , with a strong understanding of clinical trial processes and regulatory requirements. + Proven ability to manage multiple ... Senior Clinical Research Associate ICON plc is...and site management, with proficiency in relevant clinical trial software and tools. + Excellent… 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 ... Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- ICON Clinical Research (PA)
- …a Senior Clinical Research Associate . + In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. + Strong organizational and ... clinical development. We are currently seeking a Senior Clinical Research Associate or Clinical ...protocol compliance, data integrity, and patient safety throughout the trial process. + Collaborating with investigators and site… more
- Merck (North Wales, PA)
- …exposure to clinical drug development with emphasis on key elements of clinical trial planning, execution, data analysis and reporting of clinical ... Skills:** Clinical Development, Clinical Research, Clinical Sciences, Clinical Trial Planning,...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- IQVIA (Philadelphia, PA)
- …bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key ... role in ensuring the successful execution of clinical trials. In this position, you will be responsible...essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site… more
- Sumitomo Pharma (Harrisburg, PA)
- …clinical research program with minimal direction + Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing ... seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The … 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