CRA II – Home Based

September 7, 2012 by · Comments Off on CRA II – Home Based
Filed under: Clinical Research 

Clinical Research Associates II

Permanent Multiple Positions

Home based

Lavoro per una delle CRO più prestigiose, cercando dei Clinical Research Associates II per viaggiare nationwide e gestire i monitoraggi secondo ICH GCP, FDA guidelines e SOPs globali. Dopo un breve periodo in ufficio a Milano, si concede il lavoro da casa.

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 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

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 Freelance Late Phase 1.0 FTE

July 19, 2012 by · Comments Off on CRA Freelance Late Phase 1.0 FTE
Filed under: Clinical Research 

International CRO:
We offer a broad range of specialised services to assist pharmaceutical, biotechnology and medical device companies to bring new drugs and devices to market faster. Our services span
the entire lifecycle of product development and can be adapted to suit small local trials or large global programs.

Job Title:
CRA Freelance Late Phases. 1 FTE

Job description:
Our global team of experts provide a full spectrum of market-leading clinical Late Phase research, real-world studies, health economics and patient reported outcomes to support our
clients’ product lifecycle, from early stage development, pricing and market access strategies, through regulatory and reimbursement approvals, labeling claims, and in-market support.
You will efficiently implement the activities of site recruitment, enrollment, site communications and Read more

Senior Clinical Research Associate (SCRA) – Home Based in Italia per CRO Internazionale

July 12, 2012 by · 5,850 Comments
Filed under: Clinical Research 

Una CRO internazionale in rapida crescita sta ricercando un SCRA home-based per un contratto di tipo permanente in una citta’ italiana grande e ben collegata.

La CRO ha ufficio a Milano e la posizione e’ aperta grazie alla promozione del SCRA in carico dello studio.

Si offrono:

  • Eccellenti opportunita’ di carriera
  • Ottimo bilancio tra lavoro e vita lavorativa
  • Un felice ed armonioso ambiente lavorativo che stimoli il raggiungimento di ottimi risultati
  • Una buona varieta’ di progetti, aree terapeutiche, fasi e Sponsor
  • Lezioni di inglese private

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 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

« Previous PageNext Page »