Sascha Tillmanns

Angestellt, Senior Clinical Program Director, Medical Oncology, SOTIO Biotech AG

Basel, Schweiz

Fähigkeiten und Kenntnisse

Clinical Development
Clinical Science
Oncology
Medical science
Clinical Research
Due Diligence
Medical Biotechnology
Proof of Concept
Pharmaceutical industry
Autoimmunity
Pharmacology
Immunology
Scientific Advice
Protocol Assistance
KOL Management

Werdegang

Berufserfahrung von Sascha Tillmanns

  • Bis heute 2 Jahre und 7 Monate, seit Okt. 2021

    Senior Clinical Program Director, Medical Oncology

    SOTIO Biotech AG

    Clinical Lead for an IL-15 superagonist in combination with CPI in advanced solid tumors: all-comers, NSCLC, mCRC, HCC, OvC, cSCC, mCRPC, phase I FiH, phase II PoC studies, clinical development plans, TPP, line manager medical team

  • 3 Jahre und 1 Monat, Sep. 2018 - Sep. 2021

    Director, Clinical Program Leader Oncology

    MorphoSys AG

    Clinical Program Leader for an anti-CD19 antibody in hemato-oncology, clinical development stragety strategy, phase 2, registrational phase 3, real-world evidence, BLA, MAA, FDA, EMA scientific advice, due dilligence, lymphoma advisory board, clinical development plans, target product profile, study protocols, reports

  • 1 Jahr und 4 Monate, Mai 2017 - Aug. 2018

    Clinical Development Consultant

    Novartis NIBR, NDA, Biopharma Excellence

    Clinical development strategy, clinical trials, receptor protein, EMA regulatory agencies briefing books, scientific advice, IMPD, ODD, publication, safety narratives, multiple sclerosis, infectious diseases, inflammatory disease

  • 2 Jahre und 2 Monate, März 2015 - Apr. 2017

    Clinical Director Immunology

    SuppreMol GmbH part of Baxalta Inc./Shire Inc.

    Representing Clinical Development in the Program Innovation Team, Receptor Protein, Fc-gamma RIIB Antibodies, Leading Clinical Subteam for SLE and IgAN Development, Responsible for Clinical Development Plan, Investigator's Brochure, Indication Strategy, Clinical Science, Orphan Drug Designations, Protocols, Study Reports, FDA/EMA Briefing Documents, Response to Deficiency Letters, KOL, DSMB and Clinical Expert Management,

  • 6 Jahre und 2 Monate, Jan. 2009 - Feb. 2015

    Medical Director

    SuppreMol GmbH

    Head of Clinical Development and Preclinical Safety. Successful Acquisition of SuppreMol by Baxalta Inc for 200 Mio EUR. Responsible for the Clinical- and Nonclinical Development Strategy for a Novel Biopharmaceutical Mode of Action in the Treatment of Autoimmune Diseases, ITP, SLE, Clinical Due Diligence, Writing of Study Protocols, IBs, Orphan Drug Designation-, FDA Briefing Documents and Response to Deficiency Letters, Clinical Expert- and DSMB Management, Line Management

  • 3 Jahre und 6 Monate, Juli 2005 - Dez. 2008

    Director, Clinical Development

    PARI Pharma GmbH

    Head of Clinical Development and Preclinical Safety. Evaluation of Clinical Programs and Development Partners for Early Aerosol Products for Infectious Diseases and Transplantation with Focus on Orphan Drug Designation, Medical Database Research, Supervision of All Clinical Trial Activities from Phase I-III and PMS Studies

  • 3 Jahre und 3 Monate, Apr. 2002 - Juni 2005

    Senior Manager Clinical Research

    Fujisawa GmbH

    Supervisor for Clinical Project Manager in the Infectious Disease Indication, Member of Clinical Development Team, Evaluation of Clinical Programs for New Anti-infective Agents

Ausbildung von Sascha Tillmanns

  • 1 Jahr und 9 Monate, Okt. 2003 - Juni 2005

    Pharmacology/Pharmaceutical Medicine

    Free University of Brussels, Belgium

  • 3 Jahre und 8 Monate, Okt. 1990 - Mai 1994

    Biology

    Philipps-University Marburg, Germany

Sprachen

  • Deutsch

    Muttersprache

  • Englisch

    Fließend

  • Italienisch

    Grundlagen

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