Quintiles cerca Senior CRA – home-based in Italy (GFR **-1410829)

July 18, 2014 by · Comments Off on Quintiles cerca Senior CRA – home-based in Italy (GFR **-1410829)
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 

Quintiles is looking for a SR CRA home based in Italy to join an huge project across the country. With the chance to work from our office in Milan or home based in Italy, as a CRA you will:

  • 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.
  • 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.

Qualifications

 We are looking for dynamic people who enjoy communicating and interacting within teams, to achieve quality deliverables.

Successful candidates have the following requirements:

  • Bachelor’s degree in a health care or other scientific discipline
  • 2-4 years of monitoring experience.
  • Experience in Oncology will be positive considered
  • Fluent in English and Italian is a must.
  • Availability to travel

Primary Location

  • Italy

Organization

  • ITA02 – Italy Product Development

 

How to apply

To apply for this job please visit the following URL:https://quintiles.taleo.net/careersection/10000/jobdetail.ftl

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 – 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

Senior Monitor Italy – Top Class Employer

November 23, 2012 by · Comments Off on Senior Monitor Italy – Top Class Employer
Filed under: Clinical Research, Miscellaneous 

Senior Monitor Italy
Office Based or Home based available

Top Global Contract Research Organization is seeking talented Senior CRAs with at least 3 years of solid experience 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/Senior CRA Italy

November 7, 2012 by · Comments Off on CRA/Senior CRA Italy
Filed under: Clinical Research 

Senior CRA

 

Italy

 

Office Based or Home based available

 

Leading global pharmaceutical service provider is looking for experienced Clinical Research Associates with at least 3 years of experience in monitoring to join their Clinical Development Department 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 degree in a science related field or certified health care professional or equivalent experience

* D.M. 2008 Certification

* Experience as CRA in clinical development 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%)

* Capability to work in a team

 

My Client can offer a competitive salary and benefits package and will support individual as well professional development in one of the most important global companies in the Industry.

 

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.

 

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

Senior CRA – TOP Global CRO

September 7, 2012 by · Comments Off on Senior CRA – TOP Global CRO
Filed under: Clinical Research 

Senior CRA Italy
Milan Office Based or Home based available

Leading global pharmaceutical service provider is looking for experienced Clinical Research Associates with at least 3 to 5 years of experience in monitoring to join their Clinical Development Department on a permanent basis to provide high quality service to the sites and to the best international sponsors.
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 degree in a science related field or certified health care professional or equivalent experience
* D.M. 2011 Certification
* Experience as CRA in clinical development 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%)
* Capability to work in a team
My Client can offer a competitive salary and benefits package and will support individual as well as professional development in one of the most important global companies in the Industry.
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

Senior Clinical Research Associate Home Based Nord o Centro Italia

August 15, 2012 by · Comments Off on Senior Clinical Research Associate Home Based Nord o Centro Italia
Filed under: Clinical Research 

Senior Clinical Research Associate Home Based Nord o Centro Italia

Il ruolo in questione e’ presso una Clinical Research organisation Europea che sta avendo un grande successo nella gestione di studi internazionali di fase 3 e 4.

Questa compagnia offre un servizio di gestione di stidi clinici che e’ focalizzato alla qualita’. Questo significa che gli sponsor usano questa CRO solo per gli studi piu’ importanti. I Senior CRA che lavorano per questa compagnia non sono sommersi di studi perche’ il requisite aziendale non e’ la quantita’ ma la qualita’!

Questo ruolo puo’ essere office based a Milano oppure homebased nel nord o centro Italia.

La compagnia offre un pacchetto retributivo molto competitivo e la possibilita’ di ricevere Read more

Senior CRA – Milano – €45000 per annum

August 15, 2012 by · Comments Off on Senior CRA – Milano – €45000 per annum
Filed under: Clinical Research 

Stai facendo il CRA da piu’ di 3 anni e pensi che i tuoi sforzi non sono ben retribuiti?

Questo e’ il momento per trovare una nuova sfida!

Il nostro cliente e’ una Clinical Research Organisation che ha un ottima reputazione in Europa. Questa buona reputazione e’ dovuta dall’ottimo servizio che questa compagnia offre ai vari sponsor e dagli ottimi stipendi che offre ai propri impiegati. Read more

Senior CRA – Office o Home Based available

July 26, 2012 by · Comments Off on Senior CRA – Office o Home Based available
Filed under: Clinical Research 

Home Based disponibile da Nord o Centro Italia

CRO leader globale è alla ricerca di Senior CRAs a tempo indeterminato con almeno 4 anni di esperienza nel monitoraggio di studi internazionali per fornire un servizio di alta qualità ai centri per i migliori sponsor internazionali. Il Senior CRA si occuperà delle attività di monitoraggio, assicurando e garantendo la qualità dei dati raccolti in loco secondo le ICH-GCP, SOP e il protocollo.

qualifiche:

  • Laurea Scientifica
  • Certificazione
  • Esperienza come CRA in sviluppo clinico di fase II – IV Read more

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