Summary
Overview
Work History
Education
Skills
Timeline
Hi, I’m

LISA EVANS

Mystic,CT

Summary

Knowledgeable Study Manager with a solid background in managing clinical trials from inception to completion. Known for fostering collaborative environments while overseeing clinical trials. Reliable team player who is change-agile and understands the importance of meeting study milestones and deadlines.

Overview

28
years of professional experience

Work History

Invivyd Biotech

Clinical Trial Manager
09.2023 - 04.2024

Job overview

  • Managed operational aspects of a large phase 3 study submitted to the FDA for emergency use
  • Fostered relationships with investigative sites, leading to increased collaboration and improved study outcomes
  • Facilitated weekly laboratory roundtable meetings with vendors and CRO to discuss sample status and to identify/resolve any potential issues
  • Performed regular Veeva TMF quality reviews to ensure inspection readiness
  • Improved data quality in clinical trials by working with data management to resolve outstanding queries
  • Created and maintained study sample tracker workbook tracking laboratory samples
  • Mitigated risks in the clinical trial process by proactively identifying potential issues and implementing corrective actions

Pfizer Inc

Study Manager
06.2007 - 04.2023

Job overview

  • Managed the operational execution of over 50 phase 1 and 2a clinical studies from start-up through database release and reporting
  • Main point of contact for CROs and vendors to ensure deliverables related to study execution were met
  • Participated in feasibility of CROs, vendors, and sites
  • Developed detailed study startup, monitoring and recruitment plans
  • Main POC for CROs and study vendors
  • Established strong relationships with key stakeholders, and fostered a collaborative working environment
  • Set recruitment targets and delivery milestones
  • Initiated drug manufacturing and packaging

Pfizer

Senior Clinical Trial Associate
01.1996 - 05.2007

Job overview

  • Supported a large volume of studies from multiple TAs
  • SME for the pTMF providing training
  • Facilitated creation of study and site level ICFs
  • Forecasted and ordered drug supplies
  • Mentored new Project/Associates
  • Led team to create new CTA colleague training
  • Regularly served on continuous improvement initiatives
  • Prepared scientific publications and abstracts
  • Collaborated with data management teams to ensure accurate and timely entry of data into the appropriate systems

Education

GCP Certification

3D Drug Development Course

University of Maine At Presque Isle
Presque Isle, ME

Associate of Science from General Studies
12-2025

Skills

  • Clinical trial oversight
  • Investigator relations
  • GCP training
  • Standard operating procedures
  • Study coordination
  • Study documentation
  • Teamwork and collaboration
  • Problem-solving

Timeline

Clinical Trial Manager

Invivyd Biotech
09.2023 - 04.2024

Study Manager

Pfizer Inc
06.2007 - 04.2023

Senior Clinical Trial Associate

Pfizer
01.1996 - 05.2007

3D Drug Development Course

GCP Certification

University of Maine At Presque Isle

Associate of Science from General Studies

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LISA EVANS