Greg Lippert
senior director clinical data management xencor@ Xencor
Del Mar, California, United States
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Greg Lippert is a highly experienced clinical development professional with over 23 years of work experience in the pharmaceutical industry. He has worked with Fortune 500 companies, biotechnology R&D companies, and CROs, overseeing clinical research vendors and implementing process improvements. Greg is skilled in vendor contract review, document creation, issue escalation, and resolution. He is certified in Medidata RAVE 5.4 and has extensive oral and written communication and presentation skills. Greg is open to challenging new opportunities and welcomes business networking.
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Emails and Phone Numbers

@biogen.com
@biogenidec.com
@gmail.com
@xencor.com
+1 617914****
+1 626305****
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About

CLINICAL DEVELOPMENT PROJECT MANAGEMENT | CDMExtensive Clinical Development and CDM experience with Fortune 500 companies, Biotechnology R&D companies and CROs. Strong experience in the oversight of outside clinical research vendors (FSP's, CRO’s, central labs, imaging vendors, etc.). Skilled in process improvement initiatives, vendor contract review and execution, document creation, issue escalation and resolution, and presenting at Investigator meetings. Medidata RAVE 5.4 Study Design 1.0 Certified. Knowledgeable in Good Clinical Practice (GCP} standards, CDISC standards, Food and Drug Administration (FDA) guidelines, International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH)guidelines, and recommended CDM best practices. Possess extensive Oral and Written Communication and Presentation skills.SCDM memberAreas of expertise:• Autoimmune• Oncology/ Support Care• Cardiovascular• Inflammation• Neuroscience• Nephrology• Bone• Psychiatric• Virology• Dermatology• Ophthalmology• Anesthesiology• Medical Devices• Phase 0 to IV Studies• Clinical Trial Design• Clinical Research Vendors• Vendor Management• Project Leadership• Risk Management• ICH/GCP Regulations• Medidata Rave EDC• FSP/CRO Lead Data Management,• COA/PRO Process Improvement• Voice of the Site Initiative• Optimization of CDMTechnical Skills: Experienced in SAS and SQL programming languages, Medidata RAVE EDC system, Clintrial, Oracle Clinical, and SAS Data Management Systems, SAS datasets/SAS viewer, JIRA, Spotfire, J-Review and Brio Query reporting tools.Open to challenging new opportunities. I welcome business networking. Please contact me at [email protected]

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Work Experience

465 N Halstead St, Pasadena, California, 91107, US

Biotechnology Research

284
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Greg Lippert's Professional Milestones

  • Clinical Data Associate Contractor (2002-01-01~2003-01-01): Successfully implemented data analysis and analysis software to optimize clinical operations and improve data accuracy.
  • senior director clinical data management xencor (2017-02-01~): Optimized data management processes, improving efficiency and accuracy of Clinical Information Management.
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Education

Point Loma Nazarene University
Point Loma Nazarene University

Business,

Communications,

Bachelors,

Business/corporate Communications

1992-1994