Giovanni La Bella - WIZBII Giovanni La Bella ha pubblicato il suo profilo professionale su WIZBII. G L

Giovanni La Bella

Clinical Data Manager/Clinical Study Coordinator/CTS Trainee

39 anni • Palermo

Riepilogo

I’m working as Clinical Data Manager/Clinical Study Coordinator/CTS trainee and would like in my career to follow the Clinical Studies from Regulatory procedures to implementation of theirs. I am Proactive and dynamic; always looking for stimulating environment; I have got passion for the change and I am always oriented to improvement myself; I learnt work with a strategic thinking. I enjoy work with people and my positive personality has allowed me to always establish good relationships with my Supervisors and Colleagues. I would like to work in Pharma Company o CRO in Clinical Research.

Competenze

• Strong Technical-Scientific Background And I Am Self-motivated, Focused On My Professional Goals, Proactive And Very Well Organized In A Work Environment. • Ability To Work On Multiple Projects, Respect Of The Deadlines And Attention To Details, Acquired During My Work Experiences • Good Knowledge Of Regulatory Aspects And Clinical Studies - Clinical Trials, I Am Able To Update CRF And Clinical Database, With Clinical Data. • I Can Bring My Strong Scientific, Regulatory And Clinical Background Gained Through The University Career And Post-Graduated Master Courses, My Positive Attitude And New Ideas To Improve A Current Process And Strategy, Because I Think The Innovation Can Be The Key Of Success In The “close” Future Pharmaceutical World. • Good Communication And Outcomes Exposure Skills • Good Relationship With Other Colleagues And External Partners • Good Ability To Collaborate With Different Teams And Good Listening Skills, Acquired During My Work Experiences • Good Cooperation With Everyone And Ability To Improve My Skills • Goal Orientation • Good Management And Organizational Skills Working In Team And Individually • Ability To Work In Team To Provide Solution • Good Knowledge Of Operating Systems: Windows, Mac OS. • Strong Ability In Word, Power Point, Excel, Access, Internet, Outlook And Scientific Research Tools.• Presentation Meeting In European Institute Of Oncology (IEO): My Experience In Clinical Research. •I Worked In European Institute Of Oncology IEO, Where I Known And Learnt The Methodologies, The Ethical / Regulatory Normatives And The Procedures To Plan And Manage A Clinical Study; Furthermore I Followed, Collected And Processed The Clinical Data. • In IEO, I Known The Different Characteristics And Types Of Clinical Studies And Their Goals In The Development Of A Drug In Oncohaematology, Within The Data Management Service That Supports All Projects In Institutional Clinical Research. • And Update IEO’s Databases Related To Clinical Trials And Clinical Data • I Have Developed My Skills To Work On Multiple Projects According To The Deadlines With Attention To The Details During My Internship As Master Thesis Student At The Laboratory Of The University And I Have Developed My Skills To Create A Very Good Relationship With All Kind Of Costumers As Well As With Sales Representatives When I Worked As A Pharmacist For 7 Months In Milan. • I Supported The Working Team, Doing My Job With The Utmost Attention And Accuracy For The Responsibilities I Had In My Duties. • I Developed A Strong Technical-Scientific, Regulatory And Clinical Background About Drugs, Dosage Forms And Clinical Study – Clinical Trials. • I Have Developed My Skills To Work On Multiple Projects According To The Deadlines With Attention To The Details During My Internship As Master Thesis Student At The Laboratory Of The University And I Have Developed My Skills To Create A Very Good Relationship With All Kind Of Costumers As Well As With Sales Representatives When I Worked As A Pharmacist For 7 Months In Milan. • I Supported The Working Team, Doing My Job With The Utmost Attention And Accuracy For The Responsibilities I Had In My Duties. • I Developed A Strong Technical-Scientific, Regulatory And Clinical Background About Drugs, Dosage Forms And Clinical Study – Clinical Trials.

Esperienze

Clinical Data Manager/Clinical Study Coordinator/CTS trainee

06-2018 - OraServizi per la personaI known and Learnt the Methodologies, the Ethical / Regulatory normatives and the procedures to plan and manage a Clinical Study; furthermore I followed, collected and processed the Clinical Data. I Prepared Hematologic tissue samples and sent to Central Laboratory chosen by Sponsor. I dealt with accounting of Drug assigned to the patients enrolled in the Clinical Studies and of the one back returned. I Sent Anatomopathology Reports and other Clinical Reports to Pharma Company, such as required by Protocol of the Clinical Studies. I dealt with assign of drug to the patients enrolled in the Clinical Studies, and of registration of new patients in the Clinical Studies open to enrollment still. I communicated to the sponsor new patients enrolled. I Updated Case Report Forms (CRF) and sent it to Sponsor: Verification and review of Adverse Events, Serious Adverse Events, Concomitant Medications and corresponding illnesses to confirm accurate Data reporting in accordance with the protocol. I Communicated with Clinical Monitor often to reviewed CRF and managed the CRA’s accesses in IEO. I Supported Oncohematological physicians to developed the Clinical Studies, respecting of patients and of Clinical Protocol of Studies. I Known the different characteristics and types of Clinical Studies and their goals in the Development of a Drug in Oncohematology, within the Data Management Service that supports all projects in institutional Clinical Research I dealt with the Database Update of the Oncohematological Diseases, Lesions and, their Etiopathogenetic characterics that are observed since January 2018 to estimate the possibility of starting new Clinical Studies sponsored by Pharmaceutical Companies; but also helping physicians to understand if to spend more their time about some Oncohematological Diseases. I Updated Database of Leukaemia Diseases too: AML, CML, ALL, MDS and Myelofibrosis Disease.

Farmacista

03-2017 - 09-2017 Servizi per la personaPharmacist trainee, Pharmacy Europea, Cologno Monzese, Milan. Management of sales relationship with sales rapresentatives magement of pharmaceutical products management of warehouse

Tesista interno

11-2014 - 03-2016 Tesi Sperimentale presso il Dipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF) dell’ Università degli Studi di Palermo: Studi di Somministrabilità della Fluoxetina attraverso la cavità orale e progettazione di compresse matriciali buccali -Prove di solubilità della Fluoxetina in diversi buffers salivari artificiali, studi di permeabilità attraverso mucosa sublinguale e buccale mediante l’uso di celle di Franz, quantificazione del farmaco permeato mediante spettrofotometria Uv-vis. -Progettazione di tre compresse matriciali buccali a rilascio controllato (Adhesive Drug Delivery Systems - ADDS),studi di velocità di rilascio della Fluoxetina da ADDS e quantificazione del farmaco inglobato in ADDS con UV-vis.

Tirocinante

01-2014 - 08-2014 Servizi per la persona-Supporto nella gestione del magazzino e mantenimento dei rapporti con i clienti e i fornitori. Gestione di carico e scarico dei prodotti venduti in farmacia. -Supporto nella preparazione galenica, nella spedizione delle ricette, nella gestione del registro degli stupefacenti e nel servizio al banco e capacità di vendita. -Apprendimento delle norme vigenti nella gestione della farmacia.

Livelli di formazione

Università Cattolica Del Sacro Cuore Di Roma

2018 - 2018 Rome, Italy, RomeServizi per la personaMaster di II livello in Sviluppo Preclinico e Clinico del Farmaco: aspetti Tecnico Scientifici, Regolatori ed Etici

Alma Laboris

2017 - 2017 Milan, Metropolitan City of Milan, Italy, MilanGestione di progetti / Prodotto, MarketingManagement e Marketing Dell'Industria Farmaceutica

Sida Group - Formazione Manageriale

2016 - 2016 Palermo, Italy, PalermoMarketingAttestato di lingua inglese rilasciato dalla Dublin City University

Università degli Studi di Palermo

2004 - 2016 Palermo, ItaliaVoto di Laurea: 104

Le mie qualità

Comunicatore/trice
Indipendente
Intraprendente
Spirito di squadra

Lingue parlate

  • Italiano

    Madrelingua

  • Inglese

    Avanzato

I miei sogni

Dopo gli studi

Lavorare in Aziende Farmaceutiche Multinazionali o CRO in ambito Ricerca Clinica, Direzione Medica o Medical Affairs Department; come CTA/CTC/CRA o ruoli simili

Trasforma il futuro in successo.
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