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Uwe Meya

Vice President International Clinical Development

Chief Medical Officer bei Minoryx Therapeutics S.L.

Basel, Basel-Town, Switzerland

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Uwe Meya's Email Addresses & Phone Numbers

Uwe Meya's Work Experience

Lupin Atlantis Holdings SA

Vice President International Clinical Development

January 2015 to Present

Schaffhausen / Switzerland

Biotie Therapies

Vice President Clinical Development

November 2007 to January 2015

Hoffmann-La Roche AG

Head Research Portfolio Management

January 2005 to October 2007

Uwe Meya's Education

Freie Universität Berlin

Clinical Psychiatrist Psychiatry

1983 to 1986

RWTH Aachen University

Clinical Neurologist Neurology

1980 to 1983

RWTH Aachen University

Staatsexamen Medicine

1973 to 1980

Uwe Meya's Professional Skills Radar Chart

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Outspoken
Inspiring
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44% Left Brained
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Uwe Meya's Estimated Salary Range

About Uwe Meya's Current Company

Lupin Atlantis Holdings SA

Responsible for implementing global clinical trial strategy and management of all clinical studies being conducted outside of India. Co-ordinate CROs as well as clinical trial sites for ensuring success of clinical operations plans. Co-ordinate the efforts of internal and external resources to ensure timely patient recruitment, trial selection, trial plan optimization and execution of trials.

Frequently Asked Questions about Uwe Meya

What company does Uwe Meya work for?

Uwe Meya works for Lupin Atlantis Holdings SA


What is Uwe Meya's role at Lupin Atlantis Holdings SA?

Uwe Meya is Vice President International Clinical Development


What is Uwe Meya's personal email address?

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What is Uwe Meya's business email address?

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What industry does Uwe Meya work in?

Uwe Meya works in the Biotechnology industry.


Who are Uwe Meya's colleagues?

Uwe Meya's colleagues are Arvind Mathur, Sandra Single, and thierry Volle


About Uwe Meya

đź“– Summary

Board-qualified Neurologist and Psychiatrist with 5.5 years of clinical tenure in academia. Long-standing experience (since 1986) in industry, with 24 years in Clinical Research & Development for neurology and psychiatry indications. Additionally two years experience serving as clinical liaison to pain / genito-urinary (GU) discovery group with projects in sensory dysfunction/pain for therapeutic applications in various GU indications. Large breadth and depth of clinical research & development experience: Responsibility for clinical studies from first-into-man up to pre-registration, and review of regulatory filing documents Clinical responsibility for diagnostic/biomarker study Covering multiple indications in Neurology (Epilepsy, Pain, Multiple Sclerosis, Migraine, Parkinson’s disease, Restless Legs Syndrome, Stroke, Traumatic Brain Injury) and Psychiatry (Depression, Anxiety, Alzheimer’s disease, Psychosis, Cocaine Addiction) Setting up Advisory Boards for Alzheimer’s and Parkinson’s disease Broad experience in in- and outlicensing and M&A activities for CNS indications. Led Schering AG’s Global Clinical Development Team for CNS (1990-1992) Led F. Hoffmann-La Roche AG’s Disease Area Strategy Team Neuroscience since inception in 2001 until 2004 with two strategic presentations to Pharma Executive Committee in 2002 and 2004 Led one of the R&D initiatives of “Roche in 2015”, ie. “Disease Area Focus” In 2002, received Roche Global Development Leadership Award Since 2005, expanded knowledge base by joining Pharma Research Strategy group, with responsibility for all Roche Therapeutic Areas: Co-ordinating the preparation of consistent, high quality Disease Area (DA) and Therapeutic Area (TA) strategies Improving and enhancing the Portfolio Assessment process Designing and conducting key portfolio meetings: Annual Research Portfolio Review Therapeutic Protein portfolio review Specialties:Central Nervous System Clinical Research & Development In-/outlicensing Translational Medicine & BiomarkersVice President International Clinical Development @ Responsible for implementing global clinical trial strategy and management of all clinical studies being conducted outside of India. Co-ordinate CROs as well as clinical trial sites for ensuring success of clinical operations plans. Co-ordinate the efforts of internal and external resources to ensure timely patient recruitment, trial selection, trial plan optimization and execution of trials. From January 2015 to Present (9 months) Schaffhausen / SwitzerlandVice President Clinical Development @ Responsible globally for exploratory clinical research and development activities of the company portfolio. The current strategic focus of the company is to conduct small, efficient studies that are data rich to establish proof of concept and determine optimal dosing before moving into larger pivotal efficacy studies. From November 2007 to January 2015 (7 years 3 months) Head Research Portfolio Management @ • Co-ordinate the preparation of consistent, high quality Disease Area (DA) and Therapeutic Area (TA) strategies throughout Pharma Research; assure TA/DA strategies are consistent with Pharma Research Strategy • Co-ordinate the 6-month review of the progress against goals for the Research Portfolio Strategy/Operational plans From January 2005 to October 2007 (2 years 10 months) Leader, Neuroscience Disease Area Strategy Team @ • Provide Head of Pharma with bi-annual formal Disease Area Strategy over next 10 years • Develop and then communicate agreed Disease Area strategy to decision bodies and key functions • Regularly monitor competitive environment and provide adjustments to the strategy as needed • Track status of Disease Area portfolio vs. decided strategy • Lead this Disease Area Strategy Team to act efficiently as advisory board for all CNS Licensing activities From October 2001 to December 2004 (3 years 3 months) Clinical Research & Licensing Liaison Manager CNS @ • Formal and informal interaction with Research and Non-Clinical Development in order to optimize the integration of the clinical development dimensions into the research activities o Address emerging medical needs and develop Target Product Profiles o Member of CNS Research Global Portfolio Committee, provide Development input into target selection and target evaluation • Responsible globally (US and “rest of world”) for the clinical development contribution to all CNS Early Clinical Development Teams, up to and including proof-of-concept studies • Evaluate clinical component of licensing opportunities and represent Roche as clinical expert for out-licensing activities From July 1999 to December 2004 (5 years 6 months) Head of Therapeutic Area Nervous System, Clinical Research (Europe) @ Managing a team, composed of Clinical Research Physicians, Clinical Research Scientists, CRAs and assistants • Responsible for all clinical development in CNS for “rest of world” (ex-USA) • Overseeing staff in conducting phase II and III studies in o Epilepsy o Alzheimer’s disease o Pain o Schizophrenia o Parkinson’s disease o Traumatic brain injury • Overseeing staff in preparing regulatory documents (Clinical Expert Reports, Integrated Efficacy and Safety Summaries) for EMEA review of one compound each in o Alzheimer’s disease o Parkinson’s diasease From December 1996 to June 1999 (2 years 7 months) Head of International Clinical Reseach CNS (Europe) @ From October 1995 to December 1996 (1 year 3 months) Head of Clincal Development CNS (Europe) @ From January 1993 to September 1995 (2 years 9 months) Medical Advisor / Head of Clinical Psychiatry (Europe) @ From February 1986 to December 1992 (6 years 11 months) Clinical Psychiatrist, Psychiatry @ Freie Universität Berlin From 1983 to 1986 Clinical Neurologist, Neurology @ RWTH Aachen University From 1980 to 1983 Staatsexamen, Medicine @ RWTH Aachen University From 1973 to 1980


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In a nutshell

Uwe Meya's Personality Type

Extraversion (E), Sensing (S), Thinking (T), Perceiving (P)

Average Tenure

3 year(s), 8 month(s)

Uwe Meya's Willingness to Change Jobs

Unlikely

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