Senior Site Manager, Oncology - Boise, United States - Idaho State Job Bank

Description

Senior Site Manager, Oncology (1 of 4) at J&J Family of Companies in Boise, Idaho, United States Job Description Senior Site Manager, Oncology (1 of W Description Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies is recruiting for a Senior Site Manager, Global Clinical Operations

• Oncology, to be remote in the United States.

A Site Manager II (SM II) serves as the primary contact point between the Sponsor and the Investigational Site.

A SM II is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.

Responsibilities may include assisting with site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities.

Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while performing trial related activities for assigned protocols.

A SM II may also be involved with process improvement, training and mentoring of other Site Managers. At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it.


Learn more at (file:
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Outlook/JHNHJA6O/and follow us @JanssenGlobal. Janssen Research & Development, LLC is part of the Janssen Pharmaceutical Companies.


Key Responsibilities:
+ Acts as primary local company contact for assigned sites for specific trials. + May participate in site feasibility and/or pre-trial site assessment visits + Attends/participates in investigator meetings as needed. + Responsible for driving activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies. Responsible for the implementation of analytical risk based monitoring model at the site level and t To view full details and how to apply, please login or create a Job Seeker account