Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

Senior Clinical Research Associate

Company: Chiltern
Location: Milan Area, Italy
Reference: IT-SRCRA-16
Closing Date: 31 Jan 17
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

Chiltern is Europe’s largest privately owned Clinical Research Organization, with over 4200 employees and 47 offices throughout Europe, both Eastern and Western, North America and in Asia. We have worked in virtually every therapeutic area for all the major pharmaceutical companies and very many of the smaller ones. The Chiltern Source department currently looking for a SRCRA to work homebased or Chilern Office, Milan Area.

Requirements:

RESPONSIBILITIES:

To prepare and conduct all site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits in accordance with study monitoring plan and client’s SOPs.

Develop and maintain good working relationships with assigned study sites in order to effectively manage each site through the clinical trial and be proactive in dealing with any issues, e.g. recruitment

Document all site visits within visit reports in a timely manner.

Appropriate follow-up with sites after monitoring visits to document findings and resolution of identified issues.

Be an integral team member and support the study team to ensure the smooth-running of the clinical trial.

Update all Client Clinical Trial Systems as required to provide effective study status updates for assigned sites

REQUIREMENTS:

At least with 3 years working experience in a similar position at pharmaceutical company or CRO

Health care or Health Sciences graduate

Experience in performing all visits types: SQV, SIV, SMV, and COV

Experience across a number of phases and therapeutic areas

Knowledge and experience of Regulatory and Ethics Committees submissions.

Competence using electronic systems e.g. CTMS, eCRF

Basic IT competence required (email, internet, word, excel)

Good standard of oral and written English

INFORMATIVA


(articolo 13 Decreto Legislativo n. 196 del 30 giugno 2003, Codice in materia di dati personali)

La informiamo che i suoi dati saranno trattati per le sole finalità di selezione. I suoi dati non saranno diffusi e potranno essere comunicati ad altre società del gruppo all’interno della EU. Ai sensi dell’articolo 7 del Codice per esercitare i suoi diritti può scrivere al Titolare dei dati : Chiltern International s.r.l., Via Montecuccoli 20/1 20147  Milano. E-mail: Italian.info@chiltern.com

INFORMATIVE NOTE


(sec. 13 of Legislative Decree no. 196 of 30 June 2003, Personal Data Protection Code)

We inform you that the archiving and processing of data referring to you are carried out in order to recruitment process. Your data will not be disseminated in any case and they may be disclosed to other companies within the EU According to sec. 7 of the Code, to exercise your rights you can write to the Data Controller: Chiltern International s.r.l., Via Montecuccoli 20/1, 20147 Milano. E-mail: Italian.info@chiltern.com

Apply for this job: Senior Clinical Research Associate

Contact Information:

Address:  Spain
Centro Empresarial, Euronova, 3 Ronda de Poniente, 0,2º, 28760 Tres Cantos, Madrid, Spain

Spain
Tel:  +34 91 187 27 00
Fax:  +34 91 187 28 49
Website:  Visit Our Web Site

Advertising
Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.