Thomas Tzschentke

Vorlesungen, Seminare und Praktika für Master-Studenten

• Management of external pharmacology studies (CROs and academic partners) • Extensive experience with initiation and coordination of external collaboration networks (KOLs, academic partners), extensive personal KOL network • Lead of work package of large EU-funded consortium (IMI-PainCare) • Extensive experience with writing preclinical parts of regulatory documents (study reports, IB, IMPD, CTD, PSUR, DSUR) • Regular attendance at scientific meetings and conferences

• Extensive and in-depth experience with late stage development and marketed products support • Extensive interaction with Clinical Development, Medical Affairs, Marketing, Market Access, Regulatory Affairs and Drug Safety • Large number of high-profile scientific publications • Extensive experience with initiation and coordination of external collaboration networks • Experience with writing preclinical parts of regulatory documents (study reports, IB, IMPD, CTD, PSUR, DSUR)

• Extensive and in-depth experience with preclinical abuse liability assessment (see below) • 8-factor analysis • member of Cross Company Abuse Liability Council • formal aspects of handling controlled substances (secure storage, documentation, yearly reports to authorities)

• Experience with organizational aspects (budget, leadership) on a departmental level

• Extensive and in-depth experience with scientific assessment of in-licensing/partnering options – Numerous full due diligences and early assessments • Management of external pharmacology studies (CROs and academic partners)

• Supervision of up to 8 technicians • De novo set-up of a new laboratory incl. several animal models • Extensive and in-depth experience with models for preclinical abuse liability assessment (see below) • Patents • Regular attendance at scientific meetings and conferences

• Extensive and in-depth experience with scientific assessment of in-licensing/partnering options - Full due diligences and early assessments • Extensive experience as pharmacology representative in late stage development teams • Experience with writing preclinical parts of regulatory documents (study reports, IB, IMPD, CTD, PSUR, DSUR) • Large number of high-profile scientific publications (incl. experience as pharmacology publication strategy lead for development compounds); patents

• Management of early-stage (LF/LO) projects • Extensive experience as pharmacology lead in early-stage (LF/LO) projects

Neurobiologie, Pharmakologie, Physiologische Psychologie, Parasitologie