Sascha Tillmanns
Angestellt, Senior Clinical Program Director, Medical Oncology, SOTIO Biotech AG
Basel, Schweiz
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
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