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

Categorie protette: Clinical Research Associate, anche Junior, per multinazionale farmaceutica

June 11, 2013 by · Comments Off on Categorie protette: Clinical Research Associate, anche Junior, per multinazionale farmaceutica
Filed under: Clinical Research 

Kuber & Partners, specializzata nella ricerca e selezione middle e top management, seleziona per importante multinazionale, leader nel settore farmaceutico, un Clinical Research Associate, appartenente alle categorie protette.

REQUISITI :
Laurea in materie scientifiche o professioni sanitarie, precedente esperienza come CRA o come Clinical Trial Assistant o Clinical Study Assistant, buona conoscenza della lingua inglese, attenzione ai dettagli, capacità organizzative, familiarità con la terminologia medica, buone capacità interpersonali, capacità di lavoro in team. Disponibilità ad eventuali trasferte nazionali.

Si prenderanno in considerazione anche figure junior.

RUOLO :
La risorsa inserita in un ambiente di lavoro dinamico ed internazionale si occuperà insieme al suo gruppo, di monitoraggi di studi farmaceutici, interfacciandosi con i medici, cliniche e pazienti. Gestione documentale, clinica, report.

Luogo di lavoro: Milano.

Tipologia contrattuale: tempo indeterminato. Formazione. Possibilità di crescita.

Azienda strutturata, dinamica, ottimo clima interno, leader nel settore di riferimento.

 

Se interessati mandare il cv a : sbergamaschi@kuber-partner.it
LA RICERCA HA CARATTERE DI URGENZA.

Il presente annuncio si rivolge a candidato di entrambi i sessi (L. 903/77). L`interessato invia la propria candidatura rilasciando specifico consenso al trattamento dei dati personali, ai sensi della L. 196/03.

L`informativa sulla privacy è disponibile nel sito: www.lavorint.it/privacy
AUT MIN 1236-SG 2004 sez. 1

 

 

Clinical Operations Manager Italy – CRAs Manager for International CRO

June 9, 2013 by · Comments Off on Clinical Operations Manager Italy – CRAs Manager for International CRO
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:
Clinical Operations Manager Italy – CRAs Manager

Job description:
To manage, under the direction of the Vice President of Clinical Operations, the standardization, implementation and development of company-wide tools, training and processes for Clinical Operation Department.

RESPONSIBILITIES:

Tasks may include but are not limited to:

  •  To work with the Clinical Operations Managers and Training Department to design CRA training materials and programs
  • To work with company departments in the design and application of standardized tools and templates
  • To develop co-monitoring procedures and standards
  • To aid in the development and writing of departmental and company-wide newsletters
  • To write and update Clinops Department company-wide SOPs, or to delegate the writing of SOPs to a representative
  • To coordinate efforts between the Project Management and Site Management Offices to reduce duplication of efforts and standardization of processes
  • To actively participate in company meetings
  • To coordinate, with Human Resources, resourcing procedures and metrics
  • To coordinate, with Quality Assurance, training opportunities identified in CAPA information
  • To interact with other departments of CRO on procedural issues
  • To improve timesheet training and tools
  • To track company-wide metrics and assessments

Perform other duties as assigned.  The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

 

Requirements:

  • At least 2/3 years of experience in people management (within a CRO or global pharmaceutical company)
  • CRAs recruitment/hiring experience
  • Previous experience as CRA is mandatory (4+ years)
  • Office based in Rome would be preferable (alternatively home based)
  • Fluent in the local languages of the countries under responsibilities and fluent in both spoken and written English
  • Available asap

How to apply:
Please send your resume to cv.crasecrets [at] crasecrets.com with subject “CRA Manager – CS 130609″

CRA Junior Certified

June 3, 2013 by · Comments Off on CRA Junior Certified
Filed under: Clinical Research 

DOCS – a leading provider of global resourcing solutions to the Drug Development industry-  is recruiting in Italy for an international Pharmaceutical company!

Excellent opportunity for an Home/ Office based CRA . The role is Permanent, national monitoring for studies mainly in Oncology, CNS and Immunology areas.

The Role and your Responsibilities

As a CRA (Clinical Research Associate) your position will involve the following:
Performing initiation, monitoring and close out visits.
Collecting high quality data.
Contributing to documentation design.
Assisting the Project Manager as required.
Adhering to SOP’s, ICH-GCP and other local regulations.

What is Required

With a University degree in Biology, Biological Science, Biotechnology, or equivalent,  you will have previous monitoring experience in international studies including study start up and close out (at least 2 years).

In addition, you will also require:

Excellent knowledge of ICG GCP guidelines and expertise to review and evaluate medical data.

Fluency in English.

Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner.

Ability to produce accurate work to tight deadlines.

Computer literate with Microsoft Office.

Certification as a CRA is mandatory.

Please send your cv to alessandra.arensi@crasecrets.com

Study Start-up Associate (Contracts)

March 6, 2013 by · Comments Off on Study Start-up Associate (Contracts)
Filed under: Clinical Research, Regulatory Affairs 

A leading biopharmaceutical company  is looking for an enthusiastic and experienced  Study Start-up Associate (Contracts)

Role and Responsibilities

– Prepare study-specific Clinical Trial Agreements templates with investigators and institutions for study management teams
– Negotiate budget costs and contract language with the appropriate party at the sites
– Assist with developing a budget template and determining reasonable procedure costs after thorough reading of the protocol
– Liaise with CTA Department to resolve individual contract language regarding issues that fall outside the allowable contract terms
– Maintain status tracking tool for individual sites for each study
– Maintain open communication and participate in regular meetings/teleconferences with study teams

What is Required

– BA/BS with at least 3 years of experience in pharmaceutical clinical research including contract preparation and negotiation
– Expert knowledge of ICH and GCP guidelines
– Good communication skills are mandatory
– Demonstrated ability to be customer oriented to the investigator and site personnel in order to achieve high customer satisfaction levels
– Demonstrated ability to prioritize and manage multiple complex tasks
– Demonstrated ability to attend to detail and solve problems
– Demonstrated ability to work with multiple study sites in several therapeutic areas                                                                                                                                                                                              – English written & spoken at fluent level

What is offered

This is a great opportunity to join an international company working on a cutting-edge projects!                                                                                                                        The position is Office based (Milan) or Home base (previous experience required)
Full time for 6 months with possibility of Permanent Contract
Interesting Salary

If you’re interested , please send an English Cv at alessandra.arensi@docsglobal.com quoting the reference AS- 2400.

Clinical Research Associate, Milano Office Based

January 25, 2013 by · Comments Off on Clinical Research Associate, Milano Office Based
Filed under: Clinical Research 

Clinical Research Associate, Milano Office Based

Sono alla ricerca di un monitor per una delle CRO piu’ importanti del Mondo, per una posizione a tempo indeterminato Office Based a Milano.
Il candidato ideale risponde ai seguenti requisiti:
*Certificazione DM 2008 e successive modifiche;
*Esperienza di almeno 18 mesi monitorando autonomamente centri in tutta Italia;
*Esperienza su clinical trials interventistici di fase II-IV;
*Motivazione al cambiamento e a lavorare a Milano Office Based.
Il mio cliente offre uno dei training migliori del settore, eccellente trattamento contrattuale e un pacchetto retributivo tra i piu’ competitivi. Ottime possibilita’ di carriera future.
Se interessati inviare un CV a sergio.carito@secpharma.com
Sentitevi liberi di passare la parola e i miei contatti a quanti potrebbero beneficiare di questa ottima opportunita’.

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 – 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 – Inizia il 2013 con un Top Employer

December 21, 2012 by · Comments Off on CRA II – Inizia il 2013 con un Top Employer
Filed under: Clinical Research 

CRA II

Permanent role

Milano Office based

CRO Globale tra le Top 5 nel Mondo cerca un Clinical Research Associate II per viaggiare su tutta Italia e gestire i monitoraggi secondo ICH GCP, FDA guidelines e SOPs globali. In questo ruolo si ha la opportunità di occuparsi della gestione a 360 gradi di un clinical trial, con il supporto dei team dedicati nelle fasi di start up e per la documentazione necessaria.

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 – IV

o Avere reali competenze in inglese, a livello di comprensione e espressione orale e scritta

o Doti comunicative, di presentazione, teamwork, autonomia e precisione

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

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

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