Ingrid Moll-Schueler

I am responsible for the development, implementation and execution of training strategies, plans, programs and processes to ensure efficient product and therapeutic area training (on inflammatory bowel diseases) for global, regional and local Medical Affairs colleagues. Collaboratation with internal colleagues cross-functionally and with external HCPs is key to be successful.

* Development of processes to ensure efficient information flow and communication * Ensuring alignment of communication processes across regions * Point of contact for Regional Global Medical Affairs functions and Local Medical Directors regarding compliance needs and issue identification * Identification and support of training needs * Providing guidance for on-boarding of new Medical Directors

*Strategic responsibility and operative leadership of Medical Affairs, Clinical Trial Operations, Regulatory Affairs, Pharmacovigilance and Market Access in Austria (12 to 6 people) *Management Team member reporting to Country Manager. *Responsible Person for Scientific Service in charge of information about medicinal products “Informationsbeauftragter” according to Article 65(2) Austrian Drug Law). *Safety Officer for Medical Devices *Cross-country supervision (D, CH) & coordination of Medical Advisors

Providing guidance to a team of 5 direct reports (3 Medical Advisors, 1 Regulatory Affairs Manager, 1 assistant), overseeing and hands-on all medical activities within Takeda Austria which included support of Marketing & Sales, Medical Information, planning, controlling and analysis of post marketing surveillance studies, medical publications, training of the medical reps, regulatory submissions and pharmacovigilance

Temporary assignment in order to gain insight & understanding of Clinical Research & Medical Information from a U.S. Headquarter's perspective and into organisational structures and processes. I set up and coordinated pre-study activities for the European part of a multinational Phase IIIB study with the European affiliates and actively contributed to the development of CME programs.

• Support for Clinical Trials • Marketing & Sales Support • Medical Information • Regulatory Affairs • Pharmacovigilance • Reimbursement applications • Management of personnel and budget • KOL Management • Therapeutic areas: • Gynecology (HRT & OCs), • Oncology & haematology (breast cancer, AML, hemophilia) • Infectious diseases (antibiotics & vaccines) • Neurology & psychiatry (antidepressants, sleep inducers) • Rheumatology (rheumatoid arthritis)

Marketing Support, Medical Information and clinical trial support for therapeutic areas Cardiovascular, Endocrinology (HRT & diabetes) & Dermatology

•Ciba-Geigy Austria (until Dec. 1993): Medical Advisor & Head of Reg. Affairs • Ciba Denmark (Jan. -Dec.1994): Assistant Medical Director & Project Team Member for the evaluation of a Computer based Clinical Trial Administration System • Ciba Austria (Jan. 1995-Mar. 1997): Medical Advisor for therapeutic areas Endocrinology esp. HRT, Cardiovascular and CNS • Coordination of Local Clinical Trials

• Planning and running of Phase IV clinical trials in various therapeutic areas such as epilepsy, migraine, sleep apnoea and venous insufficiency • Presentation and publication of clinical trial results • Providing medical support to marketing, e.g. development of a computer based interactive training programme for physicians • Basic and continuous medical training of the sales reps