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

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

CRA all level per azienda farmaceutica

July 12, 2012 by · 8,732 Comments
Filed under: Clinical Research 

Kelly Services è specializzata nel reclutamento e nella selezione di personale scientifico. Kelly è in grado di reclutare professionisti per assunzioni a tempo determinato ed indeterminato, dai profili junior a quelli altamente specializzati, per i settori chimico, farmaceutico, alimentare, cosmetico, biotecnologico, medicale, ambientale e petrolchimico. Per maggiori informazioni visita il sito www.kellyservices.it.
Kelly Services, per importante azienda farmaceutica, ricerca per il proprio organico:

 

CRA all level 

Il candidato eseguirà visite di monitoraggio presso i centri di sperimentazione assicurando il corretto sviluppo degli studi clinici in conformità con le ICH/GCP, SOP e normative vigenti. Opererà a stretto contatto con gli sperimentatori presso gli enti ospedalieri e terrà rapporti con i Comitati Etici. Si assicurerà che vengano salvaguardati l’integrità dei dati ed i diritti dei pazienti, di raccogliere e controllare i dati relativi alle sperimentazioni.

Ricerchiamo candidati laureati in 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

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

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

CRA II Office/Home Based

May 9, 2012 by · 11,793 Comments
Filed under: Clinical Research 

Ciao a tutti stimati Monitor,

Lavoro con le migliori CROs internazionali in Italia e a livello internazionale.

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 2 a 3 anni e che sono disposti a lavorare Office Based a Milano, oppure home based nei pressi di Milano o Roma (o di una qualsiasi altra località ben connessa e molto vicina ad un aeroporto).

I requisiti sono:

*La certificazione; Read more

CRA Remote Monitoring

May 9, 2012 by · 9,334 Comments
Filed under: Clinical Research 

Lavoro con una tra le migliori CRO Globali su territorio italiano.

Cerco attualmente un CRA che svolga visite da remoto. La posizione è ideale per un CRA che abbia almeno 2/3 anni di esperienza, che voglia tagliare drasticamente i viaggi e che sia disposto a lavorare Office Based a Milano.

Riportando al CRA Manager, la responsabilità principale di questo ruolo è quella di effettuare attività di monitoraggio e visite a distanza in accordo con le SOPs e le regolamentazioni internazionali.

Le responsabilità comprendono la gestione, il coordinamento e il supporto alle attività di monitoraggio da remoto, incluse la Read more

Sei un CRA che viaggia troppo? Leggi qui

May 8, 2012 by · 6,147 Comments
Filed under: Clinical Research 

Sei un CRA che viaggia troppo? Leggi qui

Il ruolo del CRA e’ molto richiesto nel campo farmaceutico, ma non tutti quelli chef anno gia’ il CRA sono contenti. Questo la maggior parte delle volte e’ dovuto dall’alto numero di trasferte.

Alle volte lavorare per compagnie nazionali o internazionali non significa niente, perche’ dipende molto dal tipo di struttura e line manager con cui si lavora.

Il ruolo in questione e’ presso una CRO internazionale che Read more

« Previous PageNext Page »