Clinical Research Associate
celerion
Vienna, Austria
vor 7 Tg.

Celerion is the leading global provider of outsourced early clinical research services. Customers include the leading global pharmaceutical companies as well as a number of biotechnology and small to midsized pharmaceutical companies.

provides these services through three clinical research units ( Phase I units ) with over 600 beds located in the US and Europe.

In addition, Celerion provides clinical research services through partnerships with other clinical research units in North America, Europe and Asia.

Supporting our clinical work are two world class bioanalytical laboratories located in Europe and the US.

Celerion compliments the above services by a specialized department, which coordinates complex global studies, patient studies, and vaccination trials.

Our focus is on the development of innovative pharmaceuticals with the goal of enabling companies to reach early decisions concerning which compounds to progress further into clinical development.

Celerion sites are located in North America, Europe and Asia as follows :

U.S. Lincoln, Nebraska; Phoenix, Arizona; Philadelphia, Pennsylvania

Canada Montreal, Quebec

Europe Belfast, Northern Ireland; Zurich, Switzerland; Vienna, Austria; Berlin, Germany; Paris, France

Asia Seoul, Korea; Singapore, Indonesia

For Vienna, Austria we a looking for a

Clinical Research Associate (m / f)

The Clinical Research Associate (CRA) will perform monitoring and site management activities for clinical trials, clinical investigations and other interventional or non-interventional studies.

Primary Responsibilities

Clinical monitoring and site management for national and international clinical studies of phases I-IV

Regulatory activities with authorities, ethics committees and investigators

Project management support and in-house activities for clinical research projects

Sponsor communication and contact

Knowledge / Skills / Education / Licenses* :

  • BA / BS degree in biomedical-related field, life sciences or equivalent field
  • Two years working experience in clinical research, as a CRA, Study Nurse or related profession preferred
  • One year experience in on-site monitoring preferred
  • Excellent oral and written communication skills in English and German; knowledge of other languages advantageous
  • High level of organization, multi-tasking, judgement, and keeping to timelines
  • Profound knowledge of ICH-GCP and other relevant regulatory requirements
  • Flexible and willing to travel up to 70%
  • Anticipate & prevent problems. Able to create backup plans
  • Equivalent education and experience will be considered.
  • Position Location : office based in Vienna, Austria

    Start : As soon as possible

  • The minimum monthly salary for this position according the applicable collective agreement is EUR 1958, 19 gross (for 40hrs / week);
  • overpayment depending on qualification and experience planned.

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