Mark Loudon Email & Phone Number
Strategic Program Manager @ USDM Life Sciences
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Mark Loudon Location
- Lynden, WA, US
Mark Loudon Work
- Strategic Program Manager @ (January 2025 - Present)
- CEO. Pharmacovigilance and Regulatory Systems Consultant @ (October 2024 - January 2025)
- Advisory Director, Life Science Advisory @ (November 2020 - October 2024)
- CEO. Pharmacovigilance and Regulatory Systems Consultant @ (November 2018 - November 2020)
- Vice President, PV Consultant @ (October 2016 - November 2018)
- Consulting Partner and Founder @ (April 2016 - October 2016)
- Senior Director, Compliance and Risk Management Products @ (January 2012 - March 2016)
- Director, Regulatory Compliance @ (March 2004 - January 2012)
- Executive Director, Regulatory Affairs @ (May 2002 - March 2004)
- Associate Director, Medical and Regulatory Systems @ (September 1997 - May 2002)
- Various in Medical and Clinical and Regulatory Systems @ (January 1989 - September 1997)
- Programmer @ Agathos Systems (January 1982 - January 1986)
Mark Loudon Education
- University of Kent
BSc (Hons) (Computer Science)
1982-1985
Mark Loudon Skills
- Pharmaceutical Industry
- Clinical Research
- 21 CFR Part 11
- Regulations
- Informatics
- Regulatory Affairs
- GCP
- Sop
- Clinical Trials
- Regulatory Submissions
- Biotechnology
- FDA
- Medical Devices
- Validation
- Lifesciences
- Clinical Data Management
- CTMS
- Quality Assurance
- CRO
- Computer System Validation
- Pharmacovigilance
- GxP
- Strategy
- Cross-functional Team Leadership
- Clinical Development
- Regulatory Requirements
- Life Sciences
- Pharmaceutics
- Document Management
- Business Analysis
- Requirements Analysis
- Data Management
- SDLC
- Consulting
- U.S. Food and Drug Administration (FDA)
- U.S. Title 21 CFR Part 11 Regulation
- CRO Management
- Software Development Life Cycle (SDLC)
- Good Clinical Practice (GCP)
- Clinical Trial Management System (CTMS)
- Standard Operating Procedure (SOP)
- Research
- Management
- u.s. Food and Drug Administration Fda
- Cross Functional Team Leadership
- Project Management
- Standard Operating Procedure Sop
- Good Clinical Practice Gcp
- Public Speaking
- Great
- Cost Accounting and Bookkeeping
- Has Errors
- Sales
- Software Development Life Cycle Sdlc
- Risk Management
- Specific and Common Accounting Software Training
- Clinical Trial Management System Ctms
- u.s. Food and Drug Administration
- Software Development Life Cycle
- Good Clinical Practice
- Standard Operating Procedure
- Clinical Trial Management System
Mark Loudon Summary
- Mark Loudon, based in Lynden, WA, US, is currently a Strategic Program Manager at USDM Life Sciences. Mark Loudon brings experience from previous roles at CASCIG - Cascadia Informatics & Genetics, LLC, NNIT, CASCIG and Foresight Group International AG. Mark Loudon holds a 1982 - 1985 BSc (Hons) in Computer Science @ University of Kent. With a robust skill set that includes Pharmaceutical Industry, Clinical Research, 21 CFR Part 11, Regulations, Informatics and more. Mark Loudon has 2 emails and 1 mobile phone numbers on RocketReach.
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