- Parexel (Harrisburg, PA)
- The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... Clinical Practices (GCP), and the Sponsor's standards. The Sr . CRA is accountable for site management and monitoring,...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- ICON Clinical Research (PA)
- Senior Clinical Research Associate ...Research Associate , with a strong understanding of clinical trial processes and regulatory requirements. + ... clinical development. We are currently seeking a Senior Clinical Research Associate (CRA)...will play a critical role in overseeing and managing clinical trial activities to ensure they are… more
- Pfizer (Collegeville, PA)
- …delivery unit within the Clinical Development &Operations (CD&O) organization, the Senior Associate , eCOA Manager, Clinical Data Collection Strategies is ... this role, you will: + As part of the Clinical Data and Information Sciences (CDIS) group, an integral...process + The candidate will have significant eCOA and/or trial management experience with technical expertise in eCOA. +… more
- Parexel (Harrisburg, PA)
- **Job Purpose:** The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned ... associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study… more
- ICON Clinical Research (PA)
- …mission to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate ... 3 years independent monitoring to be considered for a Senior Clinical Research Associate . +... Research Associate . + In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.… more
- IQVIA (Philadelphia, PA)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within...activities to bring revenue forward in partnership with the senior project leader. + Identify changes in scope and… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- **Job Summary** Under the direction of the Director/ Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for the ... communication of any variances in budget forecast to the Director/ Associate Director. * Establish communication flow with CRO and...(s), as assigned. * Participates in ongoing review of clinical trial data focusing on data integrity,… more
- Cardinal Health (Harrisburg, PA)
- …Review agreements in support of various business transactions, including strategic sourcing, clinical trial services, confidentiality, Business Associate and ... other departments + Work under the general supervision of senior attorneys and exercise sound judgment as to matters...matters that require attention of Legal and Compliance Departments' senior leadership + Promote and ensure compliance with the… more
- CSL Behring (King Of Prussia, PA)
- …in an area of strategic importance to the business. You will be assisting with clinical trial financial modeling for the Clinical Operations group, as well ... Associate Director, Business Operations Management, as the **Manager, Clinical Financial Modeling** , you will be presented with...modeling. You will establish a deep understanding of the Clinical Trial process at CSL to effectively… 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