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

Junior CRA – 1 year contract ROMA

September 5, 2012 by · Comments Off on Junior CRA – 1 year contract ROMA
Filed under: Clinical Research 

Junior CRA – 1 year contract ROMA

NonStop sta collaborando con una compagnia internazionale che e’ in cerca di un junior CRA per un ruolo a tempo determinato con la possibilita’ di estensione a tempo indeterminato dopo 12 mesi.

Questo ruolo e’ ideale per una persona che ha completato la certificazione come CRA da poco e vuole farsi le ossa in una compagnia che offre un ottimo training e la possibilita’ di aggiungere un ottima esperienza sul CV.

Le richieste principali per questo ruolo sono:

Ottima conoscenza dell’Inglese
Laurea Scientifica
Certificazione come Clinical Monitor
Residenza nella regione Lazio

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

Junior Clinical Data Quality Manager Office-Based a Roma (Contratto di 1 anno)

August 9, 2012 by · Comments Off on Junior Clinical Data Quality Manager Office-Based a Roma (Contratto di 1 anno)
Filed under: Clinical Research 

DOCS, started in The Netherlands 1997, is specialized in staffing solutions for the Pharmaceutical, Biotechnology and Medical Device industries. With over 1000 employees based in our offices in over 25 countries, DOCS offers one of the worlds broadest clinical resourcing platforms.

Excellent opportunity for Junior Clinical Data Manager to join a Multinational Biopharmaceutical company based in Rome.

Job:
The Clinical Quality Data Manager will contribute to the data quality of the protocol by monitoring database quality metrics at the site level and taking corrective actions when it is necessary.

Job Location:
Rome – Office based

 

Job description:

The Clinical Data Quality Manager in compliance with 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

CRA II – Milano Office Based o Home Based da location ben collegate

July 26, 2012 by · Comments Off on CRA II – Milano Office Based o Home Based da location ben collegate
Filed under: Clinical Research 

Cerco attualmente un gran numero di CRAs di studi clinici internazionali interventistici di tutte le fasi e tutte le aree terapeutiche. Le posizioni aperte riguardano CRAs con una esperienza di monitoraggio autonomo (dopo il training) che va da 18 mesi a 3 anni e che sono disposti a lavorare Office Based a Milano oppure home based da location ben collegate.

I requisiti sono:

  • La certificazione;
  • La conoscenza delle GCP e ICH; Read more

CRA II – Milano Office o Home Based

June 29, 2012 by · 1,101 Comments
Filed under: Clinical Research 

Permanent Multiple Positions

Milan Office Based or Home Based
Leading Pharmaceutical Service Provider based in Milan is currently looking for Clinical Research Associates II to travel across Italy. You will be responsible for ensuring that data will pass international quality assurance audits, will represent the company development in the global medical research community and develops collaborative relationships with investigational sites.

Responsibilities:

You will perform all clinical monitoring / site management activities nationwide for assigned projects in accordance with the company SOPs. You will be responsible for achieving and maintaining high site performance, managing clinical monitoring activities which include the ownership of investigator sites, the selection of investigator/sites, collating Regulatory Documentation, initiating and monitoring of sites, performing site documentation verification, data collection and drug accountability in accordance with ICH GCP guidelines.

Experience:

o Ideally 2/3 years of experience as Clinical Research Associate o Ideally experience in clinical phases II – III

o Good level of English o Excellent communication, presentation, teamwork and interpersonal skills

o Compliant with D.M. 2011 Certification

This is an exciting opportunity offering extensive training and development, friendly and international work environment, career progression and a competitive salary / package. If you are interested in this new opportunity, please send your CV to Sergio.carito@secpharma.com or feel free to call me for a confidential chat, on +44 (0)207 255 6665

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

Senior CRA – Top Quality

June 29, 2012 by · 3,682 Comments
Filed under: Clinical Research 

Home based available from North or Centre of Italy

Leading global pharmaceutical service provider is looking for experienced Clinical Research Associates with at least 4 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 65 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@crasecrets.com

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

Clinical Research Associates II a Roma Home Based

June 6, 2012 by · 2,742 Comments
Filed under: Clinical Research 

Permanent Multiple Positions
Rome Home Based

Global leading Clinical Research Organization based in Milan is currently looking for Clinical Research Associates II to travel across Italy to perform and coordinate all aspects of the clinical monitoring process in accordance with ICH GCP, FDA guidelines and global SOPs.
You will be responsible for ensuring that data will pass international quality assurance audits, will represent the company development in the global medical research community and develops collaborative relationships with investigational sites.
Responsibilities:
You will perform all clinical monitoring / site management activities nationwide for assigned projects in accordance with the company SOPs.
You will be responsible for achieving and maintaining Read more

Next Page »