Jelveh Lameh
Executive with expertise in bridging Precision Medicine, Biomarker & Drug Development, In Vitro Diagnostics, Operations and Quality & Regulatory Compliance
- Role
- Instructor and Member of Advisory Board at Uc San Diego Extended Studies
- Location
- San Diego, CA, US
- LinkedIn followers
- 500 followers
About Jelveh Lameh
Executive-level scientific and operational leader with extensive knowledge in the areas of molecular diagnostics, biomarker discovery & development, molecular, biochemical, and receptor pharmacology, cell signaling, pharmacokinetics, drug discovery & development, and clinical laboratory operations. I have proven results in strategic growth planning, resource optimization and establishing infrastructure and laboratories for effective clinical trial testing in compliance with GxP and CLIA requirements. I have a track record of successful development, validation, and implementation of >100 biomarker clinical trial assays.I am a strategic and results-oriented leader with passion and integrity with proven record in organizational leadership and building high-performing teams. I am skilled in ensuring alignment and effective communication among stakeholders and influencing across boundaries. I ensure team engagement, provide mentorship, and empower associates, removing roadblocks to ensure team success. I thrive in leading and supporting teams in the development of effective solutions to complex problems in fast-paced dynamic environments.I have authored/co-authored over 50 journal articles, 7 book chapters and more than 100 abstracts.Technical and Scientific expertise in:• Molecular pharmacology• Cancer and molecular diagnostics• Companion diagnostics development• In vitro diagnostics• Clinical biomarker discovery & development• Drug discovery and development• Receptor signaling and regulation• Molecular, cellular and protein-based techniques• Safety pharmacology, toxicology and DMPK• Pain, neuropsychiatric and neurodegenerative disease• Oncology and cancer chemotherapy• Application of data and digital in research and laboratory settings• GxP, GCLP, GMP, CLIA, CAP, IVDR and FDA regulations• Regulatory compliance• PMA, 510K, PSA submissions• Clinical laboratory operation• Team Building, Mentoring & Coaching• Project, portfolio and program management• Business development and intellectual property
Experience
Instructor and Member of Advisory Board
Jan 2010 — Present · San Diego, CA, US
Education
UC Santa Barbara
B.A.
University of California, Davis
M.S.
University of California, San Francisco
Post Doctoral Fellow
University of California, Davis
Ph.D.
Skills
- Pharmacokinetics
- Drug Discovery
- Molecular Biology
- Drug Development
- Cancer
- Biopharmaceuticals
- In Vivo
- Team Leadership
- In Vitro
- Toxicology
- Immunohistochemistry
- Clinical Research
- Cell
- Biochemistry
- Pharmacology
- Cell Biology
- Biotechnology
- Pharmaceutical Industry
- Clinical Development
- Neuroscience
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