Lynn Allman
Senior Director Regulatory Affairs at Varian Medical Systems
- Role
- Senior Director Regulatory Affairs at Varian
- Location
- Palo Alto, CA, US
- LinkedIn followers
- 500 followers
About Lynn Allman
Highly organized and detail-oriented regulatory affairs professional specializing in regulatory submissions for medical devices (both hardware and software). Over 12 years experience in radiation oncology field (clinical, research and industry). Excellent written and verbal communication skills developed through publications, grant applications, scientific presentations and teaching at senior university level. Strong interpersonal skills gained through collaborative clinical and research efforts, participation in scientific society committees, and co-supervision of undergraduate and graduate research projects. Proven ability to effectively manage time, multiple projects, and adhere to deadlines achieving Ph.D. in 3 years concurrently with diploma in Statistics while also fulfilling teaching responsibilities.
Experience
Senior Director Regulatory Affairs
Aug 2023 — Present
Education
Trinity College Dublin
Doctor of Philosophy, Cancer Biology and Radiation Biology
2007 — 2010
University College Dublin
Professional Certificate in Radiation Safety
Trinity College Dublin
Postgraduate Diploma, Statistics
2008 — 2009
Trinity College Dublin
Bachelor of Science (Honors), Radiation Therapy
2003 — 2007
The Johns Hopkins University
Master of Science (MS), Bioscience Regulatory Affairs
2012 — 2013
Skills
- Fda Gmp
- International Regulations
- Regulatory Requirements
- Iso 14971
- Clinical Trials
- Scientific Writing
- Laboratory
- Cancer
- Pharmaceutical Industry
- Sop
- Fda
- Regulatory Affairs
- Lifesciences
- Biotechnology
- Quality Assurance
- Oncology
- Statistics
- Quality System
- Molecular Biology
- Medical Devices
- Clinical Research
- Medical Device Quality Systems
- Iso 13485
- Regulatory Submissions
- Gmp
- Life Sciences
- Science
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