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Effectively led successful project teams and departments to identify multiple drug candidates including products in oncology, inflammation and autoimmune diseases, culminating in their clinical development. Implemented successful clinical programs for drug development including biomarkers, in vitro and in vivo modeling, efficacy models of numerous diseases, pre-formulation, regulatory, clinical operations and Phase I, II and post-marketing trials. Authored numerous regulatory documents for drug investigation and approval in Europe and US. Built Medical Affairs and MSL functions, critically evaluated internal programs and licensing opportunities, and directed teams to achieve time-driven drug development targets utilizing project management skills.Specialties: Oncology, Autoimmune and Inflammatory Diseases, Supportive Care for Emesis and Mucositis, Dermatology
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Senior DirectorMedimmune Dec 2014 - Apr 2019Research Triangle Park, NcResponsible for Externally Sponsored Research for Early Development assets. -
Director, Oncology Clinical DevelopmentGlaxosmithkline Sep 2010 - Nov 2014Research Triangle ParkResponsible for Oncology Development for inhibitors of MET, BET, PI3K, evaluation of TKI-induced dermatological adverse events and treatment, clinical operations oversight. -
Director, Clinical PharmacologyGlaxosmithkline Mar 2006 - Sep 2010Responsible for Phase I Oncology kinase inhibitor development (IGFR, AKT), IBs, INDs; Phase IV Clinical Pharmacology studies for Rezonic (CINV); Filed NDA, MAA, NDS for Rezonic and Zunrisa -
Medical Director Of Medical AffairsOsi Pharmaceuticals Jan 2004 - Mar 2006Built Oncology Medical Affairs Department, Phase IV Program for Tarceva, Gelclair and Novantrone, MLR, Responsible for MSL Program, KOLs
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Director, Oncology Clinical ResearchOsi Pharmaceuticals Feb 2001 - Dec 2003Responsible for two international Phase I Oncology Programs, Designed biomarker analyses, filed 2 INDs and 2 CTAs; Reviewed in-licensing opportunities
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Senior Clinical Program HeadGlaxosmithkline Sep 1994 - Dec 2000Responsible for Phase IV and Investigator Sponsored Trials for Oncology (Navelbine, Panorex), HIV (Zidovudine, Lamivudine, Mepron), GI (Zofran), Pulmonary (Flolan) -
Director PharmacologySphinx Pharmaceuticals Sep 1990 - Sep 1994Built and led nonclinical Pharmacology Department to assess NCEs for Oncology, Psoriasis, and Inflammatory Diseases. Filed 2 INDs and 2 CTAs in four years. Served on out-licensing team.
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Senior ScientistWyeth-Ayerst Jan 1984 - Sep 1990Filed IND and hold 3 patents for Rapamycin, Screened IL-1 and LO/CO NCEs in Immunopharmacology Department
Laurel Adams, Phd Skills
Laurel Adams, Phd Education Details
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Biochemical Nutrition -
Biomedical Sciences -
Immunology
Frequently Asked Questions about Laurel Adams, Phd
What is Laurel Adams, Phd's role at the current company?
Laurel Adams, Phd's current role is Senior Director at MedImmune.
What is Laurel Adams, Phd's email address?
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What is Laurel Adams, Phd's direct phone number?
Laurel Adams, Phd's direct phone number is +130139*****
What schools did Laurel Adams, Phd attend?
Laurel Adams, Phd attended Rutgers University, University Of Tennessee-Knoxville, University Of Tennessee, Knoxville.
What skills is Laurel Adams, Phd known for?
Laurel Adams, Phd has skills like Oncology, Clinical Development, Pharmaceutical Industry, Drug Development, Clinical Research, Biomarkers, Pharmacology, Clinical Trials, Clinical Pharmacology, Ind, Biotechnology, Immunology.
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