Puneet S. Arora Md Ms Face Email and Phone Number
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Physician-Scientist and Executive Leader, Licensed, Board Certified Physician , over 15 years of drug development experience on the industry side, all phases of clinical trials, regulatory filings, multiple therapeutic areas, development strategy, due diligence and medical affairs. Executive management experience, building and leading clinical development organizations, fund raising and managing a portfolio. Experienced Team leader for multifunctional matrix teams. Early Clinical Development - translational support for early products, clinical leadership, medical monitoring, therapeutic area strategy and CDP development, business development and due diligence, IND/CTA filing, building and sustaining external resource networks and partnerships. Worked on multiple areas including Rare diseases, Diabetes, Obesity, Osteoporosis, NASH, Hyperlipidemia, Wound Healing, Immunology and Inflammation, ITP, Hemophilia and Sickle cell disease, Dermatology, CKD, Pulmonology and Ophthalmology.Late stage work - Led Phase 2 and 3, multinational trials. Experience with pharmacovigilance, safety monitoring, regulatory reporting and medical communication. Support for development execution and communication of the global scientific medical evidence plan, cross-functional and global collaborations to integrate broad medical scientific and commercial input into the development program, supporting the development of key scientific external relationships with opinion leaders. Exposure to preparation for NDA filing.Medical affairs work including RML training, Investigator Sponsored Studies and assessment and approval of scientific materials. Clinical practice, teaching and research at Health Partners and Regions Hospital in Minneapolis-St. Paul, the University of Minnesota and the Health Partners Institute for Education and Research. Advanced diabetes research at the Mayo Clinic. Strong presentation and leadership skills. Scientific presentations at national and international meetings and to regulatory authorities. Governance and leadership experience with medical specialty groups and a large non-profit advocacy group including invited testimonies to US Senate and House committees and presentations at the White House.
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Skye Bioscience Inc. -
Founder And PrincipalAmira Advisors Mar 2024 - PresentBiotechnology consulting for all phases. Clinical development and strategy, Regulatory strategy, Site and KOL management, Key documents and Safety
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Chief Medical OfficerLassen Therapeutics Nov 2021 - Jan 2024San Diego, California, Us -
Head Of Clinical, Inflammation And ImmunologySanofi Sep 2020 - Apr 2021Paris, France, Fr -
Vice President, Head Of Clinical DevelopmentPrincipia Biopharma (Acquired By Sanofi Sep. 2020) May 2019 - Apr 2021
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Senior Medical Director, Research And Early Development (Gred)Genentech Oct 2011 - May 2019South San Francisco, California, UsClinical Team Leader for early clinical studies (FIH, POC) and projects in the preclinical and pre-IND space. Internal safety monitoring Chair for early phase multinational trials. Responsibilities include business development reviews, due diligence activities, process improvement, developing and maintaining external relationships including KOLs, advisory boards, vendor evaluations and technology assessments. Clinical lead for therapeutic area strategy development. Regulatory submissions and interactions globally, including IND and CTA filing and presentation at scientific advice meetings. Support for biomarker development. Therapeutic area experience includes CV-Metabolism, Inflammation and Immunology, GI and hepatology, Hematology and Kidney diseases.Roche Key Contributor Award Roche Applause Awards for Inspiring and Influencing, Achieving ResultsGenentech Scientific Leadership Training Genentech (gRED) Mentorship Program Genentech Personal Excellence Program -
Clinical Research Medical DirectorAmgen Dec 2008 - Oct 2011Thousand Oaks, Ca, UsKey activities include:- Provide clinical scientific input during the development and execution of clinical trials- Interpret clinical trial data- Participate in safety assessments- Participate in interactions with regulatory agencies- Author study reports and regulatory submissions-Close collaboration with internal safety and epidemiology groups to support large scale postmarketing surveillance efforts- Develop key opinion leaders and make scientific presentation at advisory boards key scientific meetings and external committee meetings as delegated by GDL- Identify new clinical research opportunities- Support partner relationships- Support product lifecycle management for new indications as directed by Global Development LeaderClinical input into the following:- Regulatory interactions and documents- Safety interactions and documents- Materials to be used in Scientific Affairs- Materials to be used by the Commercial Organization- RML training resourcesMaterials Approval and Compliance ReviewsNorth American Medical Team (Medical Affairs) -
Consultant PhysicianHealth Partners Medical Group Jul 2003 - Dec 2008Bloomington, Minnesota, UsEndocrinology, Diabetes and MetabolismExperience with designing intensive insulin regimens, insulin pumps and glucose sensorsInpatient Nutrition consultationCertified Reader, Bone Density ScansCertified in USG thyroid FNAHigh Risk Pregnancy ClinicRegions Glucose Control Committee (Inpatient Diabetes), 2006-2008Best Quality Practices Committee, Regions Hospital, 2006-2007Pharmaceutical Assistance Committee, Health Partners, 2004-2008Regions-Medtronic Fellow in Multicultural Care, 2005-2008 -
Assistant Professor Of MedicineMedical School University Of Minnesota Jul 2003 - Dec 2008Minneapolis And St. Paul, Minnesota, UsClinical Scholar, Regions Hospital CampusSupervisor for Endocrinology training at Regions/Health PartnersMentor for Research ElectivesMentor for Clinical Externships
Puneet S. Arora Md Ms Face Skills
Puneet S. Arora Md Ms Face Education Details
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Mayo Clinic Alix School Of MedicineAdvanced Diabetes -
University Of California, San FranciscoIntegrated Drug Development -
Mayo Clinic Graduate School Of Biomedical SciencesClinical Research -
Nyu Grossman School Of MedicineDiabetes And Metabolism -
Southern Illinois University School Of MedicineInternal Medicine -
All India Institute Of Medical SciencesMedicine -
Modern SchoolHigh School Diploma
Frequently Asked Questions about Puneet S. Arora Md Ms Face
What company does Puneet S. Arora Md Ms Face work for?
Puneet S. Arora Md Ms Face works for Skye Bioscience Inc.
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Puneet S. Arora Md Ms Face's current role is Experienced Biotech Leader I Board Certified Physician Scientist.
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What schools did Puneet S. Arora Md Ms Face attend?
Puneet S. Arora Md Ms Face attended Mayo Clinic Alix School Of Medicine, University Of California, San Francisco, Mayo Clinic Graduate School Of Biomedical Sciences, Nyu Grossman School Of Medicine, Southern Illinois University School Of Medicine, All India Institute Of Medical Sciences, Modern School.
What skills is Puneet S. Arora Md Ms Face known for?
Puneet S. Arora Md Ms Face has skills like Clinical Trials, Clinical Development, Clinical Research, Biotechnology, Drug Development, Medicine, Immunology, Diabetes, Internal Medicine, Pharmacovigilance, Life Sciences, Endocrinology.
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