Lisa Strologo's Location
Cambridge, GB
Lisa Strologo's Work
- Vice President Regulatory Affairs @ MedSource (now Ergomed)
- Director, Regulatory Affairs @ MedSource (now Ergomed)
- Director, Global Regulatory Affairs @ Worldwide Clinical Trials
- Associate Director @ Worldwide Clinical Trials
- Regulatory Affairs Manager @ Worldwide Clinical Trials
- Senior Specialist Regulatory Affairs @ PPD
- Regulatory Affairs Executive @ DDL Fleet laboratories
- Quality Assurance Officer @ DDD Fleet Laboratories
- Principal Analyst @ Eclipse Scientific Group
- Technical Supervisor and Analyst @ Pharmaprogress s.r.l.
Lisa Strologo's Education
- Sapienza Università di Roma
Master's Degree (Chemistry and Pharmaceutics)
1992 - 1999
Lisa Strologo's Skills
- Clinical Trials
- Pharmaceutical Industry
- Regulatory Affairs
- GCP
- Drug Development
- Clinical Development
- CRO
- Quality Assurance
- Regulatory Requirements
- Regulatory Submissions
Lisa Strologo's Summary
Lisa Strologo, based in Cambridge, GB, is currently a Vice President Regulatory Affairs at ERGOMED, bringing experience from previous roles at ERGOMED PLC, Worldwide Clinical Trials and Worldwide Clinical Trials, Inc.. Lisa Strologo holds a 1992 - 1999 Master's Degree in Chemistry and Pharmaceutics @ Sapienza Università di Roma. With a robust skill set that includes Clinical Trials, Pharmaceutical Industry, Regulatory Affairs, GCP, Drug Development and more, Lisa Strologo contributes valuable insights to the industry. Lisa Strologo has 3 emails and 1 mobile phone number on RocketReach.
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