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

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

CRA II home/office based a Milano

August 9, 2012 by · Comments Off on CRA II home/office based a Milano
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.

CRA II home/office based at Milano

The Role and your Responsibilities:

As CRA you will monitor the progress of clinical studies at investigative sites, and ensure that clinical studies are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all 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 Trial Assistant (Anche senza esperienza) a Milano

June 22, 2012 by · 5,737 Comments
Filed under: Clinical Research 

Una grande CRO internazionale (con 40 sedi nel mondo) e in forte crescita in Italia sta ricercando un Clinical Trial Assistant, con tanta voglia di fare ed imparare, anche senza esperienza.

E’ un’opportunita’ che consiglio vivamente a chi voglia mettere piede nel mondo della Ricerca Clinica. Di seguito la Job Description:

 

Job Title: Clinical Trial Assistant

Il candidato si occuperà della gestione amministrativa di studi clinici.

 

Job Location:

La posizione sarà Office based a Milano (nel cuore del centro storico)

 

Job description:

I principali compiti che la CTA dovra’ espletare sono:

  • Archiviare, scansionare, fotocopiare e distribuire la corrispondenza tra i deversi dipartimenti; Read more

Clinical Research Associates II Milano o Home-Based

June 6, 2012 by · 1,274 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.
The CRA II is 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 Read more

Senior CRA Italy

June 6, 2012 by · 2,884 Comments
Filed under: Clinical Research 

Milan Office Based or Home based available

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.

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. Read more

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