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Job Details

CLINICAL RESEARCH ASSOCIATES (CRA) / Warsaw, Poland

Company: Covance
Location: Warsaw, Poland
Reference: 68895BR
Closing Date: 21 Aug 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

CRA positions available to work within our Phase II-IV Clinical Operations Teams, Early Clinical Development or through our CoSource division directly with pharmaceutical companies.

Requirements:

CRA 1 / CRA 2 / SCRA – Warsaw, Poland

As an experienced Clinical Research Associate you'll be involved in initiation, routine & close out visits concentrating on sites in Poland. Successful candidates will enjoy the benefits of working for a company that values a WORK / LIFE BALANCE!

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 Poland.

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 across Poland 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.

Duty Highlights:
  As a CRA you will manage all aspects of study site monitoring according to SOPs, GCP, and ICH guidelines, including prestudy 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:
  These roles are full time & permanent positions employed through Covance.

Keywords: Clinical Research, CRA, SCRA, Clinical Research Associate, GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, CRA II, CRA III, LCRA, Oncology, Cardiovascular, Neuroscience, Immunology, Infectious Diseases, Metabolism, Field Based, Home Based, CRO, Pharmaceutical, Warsaw, Poland


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 ASSOCIATES (CRA) / Warsaw, Poland

Contact Information:

Address:  Covance- Warsaw


Poland
Tel: 
Fax: 
Website:  Visit Our Web Site

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