Experience

Omni Tech Medical

• United States
• E-Learning Providers
• 1 - 100 Employee

• Project Manager - L&D

  • Sep 2022 - Present



Labcorp Drug Development

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Commercial Training Manager

  • Feb 2022 - Jul 2022

• Manager PK/TK

  • Aug 2020 - Feb 2022

• Supervisor I-III Study Coordination-PKTK

  • Feb 2016 - Aug 2020

  Lead a global team of 11 study coordinators that are responsible for project management tasks.Coach, mentor, and develop staff to be successful in their current roles and future aspirations.Initiate and facilitate local and global marketing, engagement, and process improvement projects to aid in the growth of the department.Independently perform study coordinator activities such as analysis and technical writing to evaluate trends in support of PK/TK studies, in compliance with appropriate protocol, Standard Operating Procedures and regulatory agency guidelines, in a timely, efficient, and quality manner.

• Associate Study Coordinator – PK/TK

  • Mar 2014 - Feb 2016

  Coordinated PK/TK studies, ensuring their compliance with good laboratory practices, Standard Operating Procedures, and regulatory agency guidelines, as applicable.Worked directly with Pharmacokineticists to analyze and interpret PK/TK data, evaluate trends, and to author and finalize the corresponding analytical reports.Reviewed non-compartmental analysis generated by Study Directors and Pharmacokineticists.Managed all components of PK/TK studies including the establishment of study protocols, amendments, PK/TK analysis agreements, maintenance of study scheduling, client relationships and expectations, internal and external communications, study timelines, archival of study data and confirmation of Sponsor satisfaction.

• Study Coordinator I-III- DMPK

  • Feb 2012 - Mar 2014

  Responsible for the coordination of study related activities in compliance with standard operating procedures, good laboratory practices, and regulatory agency guidelines.Assisted the Study Director in all administrative aspects of metabolism programs and was responsible for coordinating activities of the various groups responsible for different study phases.Prepared metabolism study protocols, amendments, schedules, and reports, reviewed data for study compliance, and facilitated post study reviews.Handled client communication throughout the studies, financial matters, and coordinated routine client visits under the direction of the Study Director.

• Study Technician I – Senior Study Technician

  • Mar 2010 - Feb 2012

  Collected and documented pertinent data including animal observations, test material administration, and clinical sample collections.Ensured that studies complied with appropriate Standard Operating Procedures, good laboratory practices, and regulatory guidelines; including monitoring animal health, humane restraint, euthanasia of laboratory animals, and collection of biological samples.Assisted in the writing of Standard Operating Procedures and training of less experienced staff.