Greg Lippert
Point Loma Nazarene University
Tell me more about Greg Lippert?
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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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]
...See MoreWork Experience
Senior Director
Director
senior director clinical data management xencor
Biotechnology Research
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.
Education
Business,
Communications,
Bachelors,
Business/corporate Communications
1992-1994Skill
Clinical Trials
Biotechnology
Pharmaceutical Industry
Clinical Development
Gcp
Clinical Data Management
Cro
Project Management
Data Management
Sop
Validation
Edc
Fda
Protocol
Ctms
Certification
Colleagues
John Desjarlais
chief scientific officer at xencor
John Kuch
Senior Vice President | Chief Financial Officer
Bassil Dahiyat
Founder | President | Chief Executive Officer
David Ramies
chief medical officer at xencor
Lydell Valdriz
vice president finance at xencor
Other Named Greg Lippert
Frequently asked questions
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Greg Lippert's social media include: Linkedin,
Greg Lippert works for Xencor
Greg Lippert's role in Xencor is senior director clinical data management xencor
Greg Lippert works in the industry of Biotechnology Research
Greg Lippert's colleagues are John Desjarlais,John Kuch,Bassil Dahiyat
Greg Lippert's latest job experience is senior director clinical data management xencor at Xencor
Greg Lippert's latest education in Point Loma Nazarene University