Jason Rusk Email & Phone Number

Boulder, CO, US

Boulder, CO

Responsible for the identification, execution and delivery of process improvement initiatives across IQVIA Biotech. Perform research and analysis to identify deviations in productivity, delivery, and quality goals, and charter improvement projects aimed to improve performance.Subject Mater Expert for IQVIA Biotech’s eTMF responsible for: providing end user.

Boulder, Colorado

Subject Matter Expert for Comprehend’s Clinical Trials Analytics responsible for providing thought leadership during sales through deployment. Perform analysis and mapping of customer requirements and recommend Comprehend applications to address gaps. Analyze recommended solutions against customer processes and recommend appropriate change management.

Boulder, Colorado

Joined the Business Optimization department and completed multiple high-profile company-wide technology-, people-, and process-related projects linked to the integration of Novella Clinical and IQVIA.- Collaborated with IQVIA to implement a new electronic Trial Master File within Novella- Created and managed a Cost Center of 102 IQVIA employees at.

Boulder, Colorado

To provide strategic leadership, organization, training, and ongoing evaluation related to Novella clinical technology and standards as applied to Data Operations. To assure operational efficiency and simplicity in the implementation, administration, and use of clinical technology to support continuous project/program profitability. To assure that Novella.

Boulder, Colorado

Understand Technology needs of all cross-functional groups and suggest, develop, and implement solutions; ensure Technology documentation (project initiation and requirements, training, SOPs, business process) is complete and coordinate Technology activities with Information Management counterpart; establish and manage Technology timelines; assess.

Boulder, Colorado

I participated in the integration of electronic data capture into OSI Pharmaceuticals. This process started as a single EDC study and then progressed into an Enterprise Adoption partnership with Phase Forward, where I was the Project Manager for the EA. I participated in the Business Process Optimization courses provided by Phase Forward and facilitated.

Boulder, Colorado

Develop, implement, and manage US and international clinical trials in accordance with OSI’s SOPs, FDA regulations, and ICH GCP guidelines; write protocols, clinical study reports, and clinical sections for Annual Reports, Investigator’s Brochures and INDs; create study-related documents, including monitoring plans, CRF completion guidelines, and.

Boulder, Colorado

Drafting protocols, informed consents, CRFs, monitoring plans, and interim/final clinical study reports; develop clinical department Standard Operating Procedures and working guidelines; participate in the writing of Investigator Brochures, and IND annual reports; coordinate the budget/contract process with contract labs and clinical investigational sites.

Greater San Diego Area

Responsibilities included: Identification and recruitment of sites to participate in CNS clinical trials; perform site selection, initiation, interim, and closeout monitor visits; participated in the collection and evaluation of study start-up documents; drafted informed consent documents; interacted with the sponsor company when required; developed.

Ab, African History

Activities and Societies: Baseball

Education record

Activities and Societies: Baseball, soccer, National Merit Society