Lisa Pearce-Collins

Lisa is one of tranScrip’s clinical operations and project management specialists and joined tranScrip as a partner in April 2019.  Lisa has worked in clinical development for 18 years. She has experienced biotech (Oxagen Ltd) and small CRO environments (P1vital Ltd) and therefore is aware of the differences of focus and approach between the Sponsor and CRO sides of clinical development. Prior to this she worked for 10 years as a software engineer and database developer and is able to use her in-depth knowledge of IT and data handling to assist in identifying and resolving issues in study Data Management.

Lisa is responsible for continuous improvement and oversight of Project Management processes across tranScrip.

In her roles as a Clinical Operations Project Manager, Lisa has mainly worked in the respiratory and CNS therapeutic areas on early phase studies (I/II/IIb). This includes management of a large Phase IIb asthma study in Eastern Europe (6 countries; 92 sites) and complex experimental medicine fMRI studies for the development of treatments in schizophrenia, Alzheimer’s disease and depression.

Prior to joining tranScrip, Lisa worked as a Clinical Operations Director, responsible for the management, development and mentoring of a team of Project Managers, CRAs and CTAs.

Since joining tranScrip, Lisa has worked on a number of projects across various indications including Women’s Health and COVID-19.

Lisa enjoys building good relationships with clients to ensure that all team members are working to achieve the project goals. She can proactively plan and manage projects, identify and mitigate risks and oversee budgets and timelines. She has extensive experience in running studies to GCP standards, including authoring SOPs, participation in MHRA inspections and client audits and development of key study documents.