Pharma Point srl cerca CRA a Milano per una Prestigiosa Multinazionale Farmaceutica (contratto di 6 mesi)

July 18, 2014 by · Comments Off on Pharma Point srl cerca CRA a Milano per una Prestigiosa Multinazionale Farmaceutica (contratto di 6 mesi)
Filed under: Clinical Research 

Pharma Point srl Società di Ricerca e Selezione del personale per il settore Farmaceutico

www.pharmapoint.it

 

PharmaPoint

 

Prestigiosa Multinazionale Farmaceutica ci ha incaricati di ricercare un CRA da inserire con contratto di sei mesi (sede Milano sud).

Il nostro candidato ideale è laureato in Discipline Scientifiche in possesso di una esperienza pregressa nel ruolo (minimo 1 anni), maturate in contesti formativi.

 

Il CRA è la persona cui affidare il compito di organizzare, seguire e controllare l’andamento dello studio clinici presso il centro sperimentale. Il CRA quindi segue la sperimentazione, visitando i centri coinvolti nella

sperimentazione e collaborando con i medici impegnati nello studio.

 

Sarà responsabile di:

  • Rapportarsi con i Comitati Etici, sottomettendo il protocollo di ricerca clinica e tutti i documenti regolatori applicabili per la corretta gestione dello studio clinico.
  • collaborare nella selezione dei centri potenzialmente interessati a partecipare alla sperimentazione clinica (Pre Study)
  • Presentare il protocollo e le procedure studio specifiche agli sperimentatori, facendo loro il training richiesto per iniziare lo studio (Initiation Visit)
  • Monitorare lo studio clinico in tutte le sue fasi, recandosi anche presso il centro per effettuare le cosiddette Visite di Monitoraggio.
  • Archiviare la documentazione studio specifica in ufficio, ed assicurare il costante aggiornamento dei documenti conservati nel centro.
  • Assicurare il continuo rifornimento del materiale di sperimentazione al centro (sia esso farmaco o altro materiale di studio)
  • Occuparsi della Drug Accountability e dell’invio dell’IMP (Investigational Medicinal product) presso il dipartimento incaricato alla distruzione.
  • Chiudere i centri quando termina lo studio (Close-Out visit)

 

Requisiti indispensabili:

  • laurea in materie tecnico-scientifiche, Vecchio Ordinamento o Specialistica del nuovo ordinamento (Scienze naturali, Farmacia, CTF, Chimica, Biologia, Biotecnologie, Medicina ed altri corsi di laurea equipollenti)
  • ottima conoscenza della Lingua Inglese e pacchetto office
  • preferibilmente almeno 1 anno di esperienza maturata come CRA e in possesso della certificazione secondo il modello DM 15 Novembre 2011
  • Disponibilità a viaggiare in Italia e all’Estero
  • Sono inoltre richieste eccellenti abilità relazionali e comunicazionali, autonomia gestionale, problem solving e team-working.

 

Si offre:

  • Contratto ccnl Chimico Farmaceutico a tempo determinato (sei mesi)

 

Sede di lavoro:

  • Milano sud

 

Come presentarsi:

  • Scrivere a l.cavalieri [at]pharmapoint.it
  • Oggetto: CRAsecrets CRA per Farmaceutica

Quintiles cerca CRA home based in Italy

July 18, 2014 by · Comments Off on Quintiles cerca CRA home based in Italy
Filed under: Clinical Research 

About Quintiles:

Quintiles logo

 

 

Quintiles (NYSE: Q) is the world’s largest provider of biopharmaceutical development and commercial outsourcing services with a network of more than 29,000 employees conducting business in approximately 100 countries. We helped develop or commercialize all of 2013’s top-100 best-selling drugs on the market.

 

Quintiles applies the breadth and depth of our service offerings along with extensive therapeutic, scientific and analytics expertise to help our customers navigate an increasingly complex healthcare environment as they seek to improve efficiency and effectiveness in the delivery of better healthcare outcomes.  To learn more about Quintiles, please visit www.quintiles.com

 

Responsibilities 

We are looking for enthusiatic people to join one of our Clinical Research Units. With the chance to work from our office in Milan or home based in Italy, as a CRA you will:

  • Monitor study progress to assure compliance with protocol-requirements, regulation and Good Clinical Practice by conducting site visits as directed
  • Participate in study development. Perform site selection, initiation, monitoring and close-out visits for a variety of protocols, sites and therapeutic areas
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations
  • Conduct initial and ongoing site, sponsor, and project staff training as necessary. Establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • Monitor study progress to assure compliance with protocol-requirements, regulation and Good Clinical Practice by conducting site visits as directed
  • Monitor and track patient enrollment and ensure the timely accurate and complete study data
  • Assist the Sponsor in problem solving and provide consultation on study related activities

Qualifications

 

  • Bachelor’s degree in a health care or other scientific discipline
  • 2-4 years of monitoring experience.
  • Fluent in English and Italian.
  • Availability to travel

Primary Location

  • Italy

Organization

  • ITA02 – Italy Product Development

Read more

Quintiles cerca Freelance Clinical Research Associate – Lombardia Italy

July 3, 2014 by · Comments Off on Quintiles cerca Freelance Clinical Research Associate – Lombardia Italy
Filed under: Clinical Research 

About Quintiles:

Quintiles logo

 

 

Quintiles (NYSE: Q) is the world’s largest provider of biopharmaceutical development and commercial outsourcing services with a network of more than 29,000 employees conducting business in approximately 100 countries. We helped develop or commercialize all of 2013’s top-100 best-selling drugs on the market.

 

Quintiles applies the breadth and depth of our service offerings along with extensive therapeutic, scientific and analytics expertise to help our customers navigate an increasingly complex healthcare environment as they seek to improve efficiency and effectiveness in the delivery of better healthcare outcomes.  To learn more about Quintiles, please visit www.quintiles.com

 

 

Key responsibilities of this role include:

  • Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
  • Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.  Escalate quality issues to Clinical Team Lead (CTL) and/or line manager.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.
  • May provide assistance to more less experienced clinical staff.

 

At Quintiles we value individuality, fresh ideas, and the contribution that our employees make to our success.  In return we offer career opportunities providing flexibility and growth across the organisation, competitive salary and benefits package, work-life balance initiatives and social events.  These are just some of the incentives we have to offer.

Read more

Keyrus Biopharma: Home based Clinical Research Associate in Italy

February 21, 2014 by · Comments Off on Keyrus Biopharma: Home based Clinical Research Associate in Italy
Filed under: Clinical Research 
As a Contract Research Organisation (CRO) and major player in clinical research, Keyrus Biopharma has been has been sharing its clinical research experience with pharmaceutical industries, food industries and biotech
companies in the development of drugs and other products such as nutritional products, medical devices, cosmetics and contrast products. Our headquarters are based in France.
Today, Keyrus Biopharma provides expertise and consultancy in all clinical research areas (monitoring, data management, biostatistics, medical writing…), and is recognized by our clients in France and abroad.
We are looking for an Experienced Clinical Research Associate in Italy, to work Home Based: Organized, with good communication skills, fluent in Spanish and English, with Life science education
(biomedical sciences, pharmacy, biology, nursing or similar) and previous experience as a CRA, your main Read more

Freelance Clinical Research Associate Medical Device a Milano

September 9, 2013 by · Comments Off on Freelance Clinical Research Associate Medical Device a Milano
Filed under: Clinical Research 

 

St. Jude Medical Italia – Multinazionale Americana leader nella produzione di dispositivi medicali – ricerca in area Milano un CLINICAL RESEARCH ASSOCIATE FREELANCE per importante studio clinico da effettuare.

Il candidato che cerchiamo ha maturato un’esperienza di almeno 3 anni negli Studi Clinici di aziende del Medical Device ed è autunomo nella verifica della documentazione del centro in base al piano di monitoraggio e rispetto ai dati riportati nei CRF.

É richiesta un’ottima conoscenza della lingua inglese orale e scritta per potersi interfacciare efficacemente con l’Head Quarter. Costituisce requisito preferenziale la certificazione Read more

Oncology, CRA II Milano Home Based Permanent

July 10, 2013 by · Comments Off on Oncology, CRA II Milano Home Based Permanent
Filed under: Clinical Research 

Oncology, CRA II Milano Home Based Permanent

Ciao a tutti stimati Monitors,

Cerco attualmente un CRA di studi clinici internazionali interventistici in area oncologia.

La posizione aperta riguarda un CRA con una esperienza di monitoraggio autonomo di almeno 2 anni e che sia disposto a lavorare Home Based da Milano.

I requisiti sono:

  • La certificazione;
  • Gestione sottomissioni e site contract negotiation; Read more

LeadCRA Oncology – Home Based Milano

July 10, 2013 by · Comments Off on LeadCRA Oncology – Home Based Milano
Filed under: Clinical Research 

Oncology, Senior CRA Milano Home Based Permanent

Ciao a tutti stimati Monitors,

Cerco attualmente un Senior CRA di studi clinici internazionali interventistici in area oncologia, che sia interessato ad un ruolo in cui si ha la possibilita’ di assumere incarichi da Clinical Project Manager, Lead CRA e che abbia la volonta’ di avere dei riporti diretti dove richiesto, a livello di line manager/Clinical Operations Manager.

La posizione aperta riguarda un Senior CRA con una esperienza di monitoraggio autonomo di almeno 3 anni e che sia disposto a lavorare Home Based da Milano.

I requisiti sono:

  • La certificazione;
  • Gestione sottomissioni e site contract negotiation;
  • Site set up and monitoring experience;
  • Mentoring or line managing junior CRA;
  • Attivita’ di Clinical Project Manager activities when required;
  • La conoscenza delle GCP e ICH;
  • Buon Inglese;
  • Buona capacita organizzativa;
  • Disposto a viaggiare;
  • Proprieta di linguaggio.

Le offerte che propongo sono sempre migliorative a livello di avanzamento di carriera, bilanciamento vita lavoro e economico. Applicare solo se seriamente intenzionati a cambiare e in linea con tutti i requisiti.

Vi prego di inviare un cv aggiornato a sergio.carito@secpharma.com A presto. Sergio.

Sergio Carito

Consultant Pharmaceutical, CRO, Healthcare & Biotech Division

Italy and Europe

Tel: +44 (0) 207 255 6665

sergio.carito@secpharma.com

http://uk.linkedin.com/in/sergiocarito

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business

Senior Clinical Research Associate – Per un 2013 di successo

December 21, 2012 by · Comments Off on Senior Clinical Research Associate – Per un 2013 di successo
Filed under: Clinical Research 

Senior CRA Italy

Milan Office Based or Home based available

Global CRO is seeking a talented Senior CRA with at least 4 years of solid experience in monitoring activities to join them on a permanent basis. You will be in charge of the monitoring activities, ensuring and assuring the quality of the data collected on site according to ICH-GCP, SOP and study protocol. You will have responsibilities of Site Management, identifying, selecting, initiating and closing-out investigational sites and acting as liaison between study site and in-house team. You will also be in charge of the Study Management, working independently and proactively to coordinate all necessary activities required to set up and monitor a study.

Qualifications:

* University Life Science Degree

* D.M. 2011 Certification

* Experience as CRA in phase II – IV

* In depth knowledge of ICH-GCP, EU and FDA requirements

* Excellent Italian and English language skills (spoken and written)

* Willingness & ability to travel (approx. 50%)

* Teamwork

My Client can offer a competitive salary and benefits package, the best training in the industry and will support individual as well professional development in one of the most important global companies in the Clinical Research.

To apply, forward your CV to Sergio.carito@secpharma.com call Sergio Carito on + 44(0)207 255 66 00 for further information and a confidential discussion of this opportunity.

Sergio Carito

Consultant Biotech, Pharmaceutical, Healthcare & CRO Division

Italy and Europe

Tel: +44 (0) 207 255 6665

sergio.carito@secpharma.com http://uk.linkedin.com/in/sergiocarito

CRA II – Inizia il 2013 con un Top Employer

December 21, 2012 by · Comments Off on CRA II – Inizia il 2013 con un Top Employer
Filed under: Clinical Research 

CRA II

Permanent role

Milano Office based

CRO Globale tra le Top 5 nel Mondo cerca un Clinical Research Associate II per viaggiare su tutta Italia e gestire i monitoraggi secondo ICH GCP, FDA guidelines e SOPs globali. In questo ruolo si ha la opportunità di occuparsi della gestione a 360 gradi di un clinical trial, con il supporto dei team dedicati nelle fasi di start up e per la documentazione necessaria.

Le candidature verranno tenute in considerazione a partire da gennaio 2013.

Esperienza:

o Idealmente 18 mesi/3 anni come Clinical Research Associate

o Idealmente esperienza in fasi II – IV

o Avere reali competenze in inglese, a livello di comprensione e espressione orale e scritta

o Doti comunicative, di presentazione, teamwork, autonomia e precisione

o Compliant con D.M. 2011 Certification

Questa è una opportunità ideale per un professionista organizzato e tecnicamente molto preparato. Si offre training e sviluppo continuo, ambiente di lavoro amichevole e internazionale, un percorso di carriera sicuro e programmato e un pacchetto retributivo molto competitivo.

Se interessati, spedire il CV a Sergio.carito@secpharma.com, +44 (0)207 255 6665.

Sergio Carito

Consultant Biotech, Pharmaceutical, Healthcare & CRO Division

Italy and Europe

Tel: +44 (0) 207 255 6665

sergio.carito@secpharma.com

http://uk.linkedin.com/in/sergiocarito

CRA II – Cambia per il meglio

December 21, 2012 by · Comments Off on CRA II – Cambia per il meglio
Filed under: Clinical Research 

CRA II – Cambia per il meglio nel settore

Permanent Multiple Positions

Milano Office based o Home based da Locations ben connesse

Lavoro per una delle CRO più prestigiose al mondo cercando dei Clinical Research Associate II per viaggiare nationwide e gestire i monitoraggi secondo ICH GCP, FDA guidelines e SOPs globali. Dopo un breve periodo in ufficio a Milano per i training, si ha la possibilità di lavorare da casa.

Le candidature verranno tenute in considerazione a partire da gennaio 2013.

Esperienza:

o Idealmente 18 mesi/3 anni come Clinical Research Associate

o Idealmente esperienza in fasi II – III

o Avere reali competenze in inglese, a livello di comprensione e espressione orale e scritta

o Doti comunicative, di presentazione, teamwork

o Compliant con D.M. 2011 Certification

Questa è una opportunità ideale per un professionista organizzato e tecnicamente molto preparato. Si offre training e sviluppo continuo, ambiente di lavoro amichevole e internazionale, un percorso di carriera sicuro e programmato e un pacchetto retributivo molto competitivo.

Se interessati, spedire il CV a Sergio.carito@secpharma.com, +44 (0)207 255 6665.

Sergio Carito

Consultant Biotech, Pharmaceutical, Healthcare & CRO Division

Italy and Europe

Tel: +44 (0) 207 255 6665

sergio.carito@secpharma.com

http://uk.linkedin.com/in/sergiocarito

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