Stefania Pirondi

Head of Clinical Innovation @ Chiesi Group

Country

Italy

City

Parma

Industry

Pharmaceuticals

Skill

Coltura cellulare, Industria farmaceutica, Clinical Study Design, Scienze naturali, Protocollo, Buona pratica clinica, Ricerca clinica, SOP, CRO, Open and clear communicator, Confident and influential approach, Make independent choices and take responsibility for own actions, medical writing activity, Biologia molecolare, Neuroscienze, Biotecnologia, Sperimentazioni cliniche, Understand the needs of others, Coordination and planning of budgets, people and time management, Recognise problems reacting quickly and effectively to resolve them

Experience

Head of Clinical Innovation

Chiesi Group

2025-7 - Present · 1 yr 3 mos

Head of Global Clinical Project Management Unit

Chiesi Group

2023-5 - 2025-7 · 2 yrs 3 mos

Parma, Emilia Romagna, Italia

Real World Evidence Program Leader

Chiesi Group

2021-1 - 2023-5 · 2 yrs 5 mos

Parma, Emilia Romagna, Italia

Lead Clinical Project Manager

Chiesi Group

2016-5 - 2021-1 · 4 yrs 9 mos

Parma, Emilia-Romagna, Italia

senior Clinical Project Manager

Chiesi Group

2014-7 - 2016-5 · 1 yr 11 mos

Parma

Study Manager

Medidata srl

2013-10 - 2014-6 · 9 mos

Modena

Management, devlopment and planning of clinical studies according to National and International law, GCP and applicable SOPs

Clinical Research Assistant

Medidata srl

2012 - 2013-10 · 1 yr

Design, planning and management of clinical studies according to National and International law, GCP and applicable SOPs ASKS Design, planning and management of clinical studies according to National and International law, GCP and applicable SOPs Project coordination, planning and logistics, including overview of budget and timelines Act as the main line of communication between the sponsor and the investigator. and maintain contact to marketing and sales department Responsible for the safety and proper conduct throughout the trial (according to protocol and all GCP procedures applicable) Verifying that source data/documents and other trial records are accurate, complete, and maintained Adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol on the CRFs

Study Designer

Medidata srl

2009 - 2012 · 3 yrs

Design, planning and management of clinical studies according to National and International law, GCP and applicable SOPs. Harmonization of differente stakeholder (i.e. customers, physicians, technical adviser) interests ti define a common project Review of specialistic literature (scientific-medical topics)

Post doctoral fellow

Karolinska Institutet

2001-1 - 2009-2 · 8 yrs 2 mos

In vivo and in vitro models for neurodegenerative diseases, test for bioactive molecules, toxicity assays and biocompatibility (nanomaterials). Activity and budget report preparation Writing activity (scientific paper and congress communcations)

post doctoral fellowship

Karolinska Institutet

2005 - 2005

Education

Università degli Studi di Modena e Reggio Emilia

Biotecnologie

1996 - 2021 · 25 yrs

Alma Mater Studiorum – Università di Bologna

Biotecnology applied to medical science

2001 - 2004 · 3 yrs

Università degli Studi di Modena e Reggio Emilia

Biotechnology

1995 - 2001 · 6 yrs

July 2009: Master Specialization in Intellectual property management Oct 2007 “M-ASTER LAB” in Innovation management at Aster S.Cons.p.a. - Bologna. Sponsored by Regione Emilia Romagna. May 2005: Ph.D. in Biotechniques in Neuro-morphophysiology, Alma Mater Stusiorum, Bologna University 2000- 2005 Collaboration MS degree and Ph.D performed in collaboration with: Neuroscience Dept. of Karolinska Institute Stockholm Postdoctoral Fellowship at Neuroscience Dept. of Karolinska Institute Stockholm. (Topics: Cell transfection of in neural cell lines)