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Job Details

CLINICAL RESEARCH ASSOCIATE II (CRA II) / Budapest, Hungary

Company: Covance
Location: Budapest, Hungary
Reference: 68278BR
Closing Date: 19 Jun 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

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

Requirements:

Home based, Budapest, Hungary.

Requirements
 CRA II:
 - 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 Hungary

USPs of CRA role:
 - Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit' targets
 - Join a stable team of CRAs in Hungary 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, Budapest, Clinical Monitor, Immunotherapy, CRA, Hungary

THERE IS NO BETTER TIME TO JOIN US!


EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.

Apply for this job: CLINICAL RESEARCH ASSOCIATE II (CRA II) / Budapest, Hungary

Contact Information:

Address:  Covance- Warsaw


Poland
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