- Manage more complex trials across multiple study types (Interventional ISR, Non-Interventional, and Non-Clinical) and various Therapeutic Areas (Oncology and Immunology). - Support International Immuno-Oncology Network (II-ON) by managing operation project set-up, budget tracking, and contracting for several large institutions.- Mentor and train Trial Managers as a subject matter expert in Non-Clinical Research (NCR) and Investigator Sponsored Research (ISR) to ensure proficiency in managing studies and maintaining systems.- Serve as a Veeva Clinical Trial Management System (CTMS) Subject Matter Expert and Super-User, effectively supporting Late Development by training new users and troubleshooting issues.- Selected as electronic Trial Master File (eTMF) Subject Matter Expert to perform eTMF effectiveness checks for trials across Late Development.- Facilitate, plan, and manage monthly Late Development Global Meeting with Trial Managers involving answering or triaging process or study-related questions and discussing relevant Late Development topics.- Maintain mentoring, training, and on-boarding responsibilities from Associate Trial Manager role.- Provide valuable input in development of Non-Interventional Research process guide and playbook.

- Operationally manage clinical trials in Non-Clinical Research (NCR) and Clinical Investigator Sponsored Research (ISR).- Lead training on NCR BMS Sponsored studies for Global Trial Specialists working on NCR BMS Sponsored studies and provide ongoing oversight and support.- Serve as an Eclipse (CTMS) Super User and Regional Trainer for Protocol Managers and Operations Leads.- Review and approve invoices from vendors for NCR and ISR studies.- Mentor and onboard new team members on the NCR team.- Train and support Protocol Managers worldwide in NCR process.- Contribute to continuous improvement in NCR processes and systems.

-Serve as a subject matter expert for Investigator Sponsored Research (ISR) study process.-Work as an Eclipse Super User and troubleshoot issues for other Protocol Specialists and Protocol Managers in GCO.- Provide training for new Protocol Specialists as an Eclipse Regional Trainer.- Manage the SUSAR mailbox and oversee the team distributing the SUSARs.- Design and improve SUSAR distribution process.- Act as a data quality champion in BMS clinical trial management system.- Manage the operational study process for non-patient enrolling Health Economics Outcomes Research (HEOR) studies for both US and Worldwide HEOR.- Collaborate with US and Worldwide HEOR Study Directors to facilitate the contracting process between BMS and external vendors.- Oversee invoicing process for assigned ISR and HEOR studies.

- Serve as a subject matter expert on MDO SUSAR distribution process.- Efficiently manage the entire ISR Oncology book of work regarding Ops Analyst responsibilities.- Conduct interviews and make final decision with interview panel on summer interns.- Manage summer intern tasks and workload to deliver results on summer projects.- Provide on-boarding and training to ensure MDO new hires can perform on responsibilities.- Project management with summer intern support for BMS study file transfer to another pharmaceutical company.- Participate in process improvement projects to increase efficiency throughout MDO book of work.- Process invoices in SAP for payment including fund management in clinical trial management system.- Quickly input clinical trial data into BMS clinical trial information management system.- Archive and route contracts for approval and signature.

Bristol-Myers Squibb, Business Operations Analyst

Created presentation for Executive Director of CSR&O to deliver. Received R&D Star Award for project output. Responsible for routing invoices for payment. Learned Eclipse system to log clinical trial information and document payment records. Input clinical trial data into BMS Trial Information Management system. Responsible for document archiving into internal records management system.