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

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

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 – 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

CRA II Home based

October 1, 2012 by · Comments Off on CRA II Home based
Filed under: Clinical Research 

CRA II Home based

NonStop sta collaborando con una CRO internazionale che e’ in cerca di una persona che abbia 18 mesi di esperienza come CRA, per un ruolo home based.

Il ruolo in questione e’ ideale per una persona che e’ gia’ molto indipendente nel ruolo di CRA e vuole entrare in un ruolo dove il line manager offre molta liberta’ lavorativa.

Questo ruolo e’ ideale per una persona che sta cercando un ruolo indipendente e la possibilita’ di trovare un ruolo che e’ home based con una compagnia che ha uffici in Italia.

La compagnia offre un ottimo pacchetto retributivo, e una media di 8-10 monitoraggi al mese.

Le richieste principali per questo ruolo sono:

Ottima conoscenza dell’Inglese
Laurea Scientifica
Certificazione come Clinical monitor
Esperienza su studi interventistici
Un minimo di 18 mesi di esperienza come CRA

Vi invitiamo a mandare il vostro CV al seguente indirizzo: j.lavarino@nonstop-pharma.it

Oppure per maggiori informazioni contattate John Lavarino a NonStop sul +44 (0)207 940 2106

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

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