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

Clinical Research Associate (CRA) in Belgium

Company: Covance
Location: Belgium
Reference: 70158BR
Closing Date: 02 Sep 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

CRA II position available to work directly with a large Pharmaceutical company in the cutting edge area of Oncology. As an Experience d CRA you'll be involved in initiation, routine & close out visits concentrating on sites in Belgium. Successful candidates will enjoy the benefits of working for a company that values a WORK / LIFE BALANCE!

Requirements:

Requirements:

- Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- Excellent understanding of Serious Adverse Event reporting
- Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in Belgium.
- Fluency English, French and Dutch

USPs of CRA II role:

- Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit' targets
- Join a stable team of CRAs across Belgium and benefit from outstanding training and development, both initially and throughout your career
- Join a company where people tend to stay for 6-10 years rather than 1-3!
- Join a genuinely friendly and supportive company where they allow individuals to take ownership of their own performance.
- ONCOLOGY Focussed

Duty Highlights:

As a CRA you will manage all aspects of study site monitoring according to SOPs, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files. Responsibilities include:

- All aspects of site management as prescribed in the project plans
- Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
- Negotiation of study budgets with potential investigators and collaboration with Covance legal department with statements of agreements
- Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.
- Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems

Other Information:

This CRA II role is a full time & permanent position employed through Covance.


Keywords: CRA II, Clinical Research Associate, Oncology, Belgium, Brussels , Clinical Monitor, Immunotherapy, CRA II, Cancer Clinical trials

Apply for this job: Clinical Research Associate (CRA) in Belgium

Contact Information:

Address:  Covance- Brussels


Belgium
Tel: 
Fax: 
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.