Experienced Clinical Research Associate Clinical Trials in Germany


Experienced Clinical Research Associate Clinical Trials in Germany

KLIFO  wants to appoint an experienced Clinical Research   Associate   into  a  dynamic   and  experienced team  within Clinical  Operations  Solutions  in  Germany. The   people   we   want   to   engage   like   to   work   in   a consulting environment and have a positive, proactive, flexible,  self-driven  and  self-confident  personality.  We can  offer  a  highly flexible,  free  and  trustful  working climate with exciting customers and projects among competent  colleagues  where  your  knowledge, experience and contribution are valuable and highly appreciated

The position as Clinical Research Associate (CRA):

The CRA has considerable knowledge and is responsible as primary contact for investigational sites, conduct of monitoring activities and for assistance of the Project Manager:

  • Continuous relationship with the Principal Investigators and trial staff to assure the success of the trial in terms of enrolment and quality
  • Visiting investigator and investigational site before a specific trial: pre-trial/site assessment visits
  • Performing initiation, routine monitoring and close-out visits
  • Elaboration of trial specific procedures
  • Participation in the preparation of trial documents for submissions to Competent Authorities and Ethics Committees/Institutional Review Boards
  • Support to data management activities
  • Assist in ensuring site compliance with protocol and trial objectives
  • Work in the clinical trial team, reporting to project manager for trial related deliverables
  • Translation/review of essential documents
  • Liaison between sponsors, investigators and vendors
  • Project management

Qualifications:

  • Minimum 2 years of experience as CRA within industry/CRO/BioTech
  • Extensive knowledge of GCP guidelines, applicable regulatory requirements, medical terminology and clinical trial processes
  • Willingness to travel
  • Excellent verbal and communication skills
  • Native speaker of German of comparable level (e.g. able to translate patient documents or ICFs into German, able to talk and email in German with site personnel)
  • B.Sc. in the life sciences field or CRA specific diploma
  • Good computer skills, ability to develop and maintain excel spreadsheets, handling of access database and to elaborate PowerPoint presentations.
  • Strong organizational and planning skills
  • Accurate and precise with attention to details
  • Ability to motivate

In addition the ideal candidate is a dedicated and collaborative team player, and fluent, spoken and written, in English.

In addition the ideal candidate is a dedicated and collaborative team player and fluent, spoken and written, in English

We offer:

  • Work within different therapeutic areas and with tasks of varying complexity
  • Work with a heterogeneous client pool (pharmaceutical companies, established biotech, inexperienced biotech, investigators/academia)
  • Build international client relations
  • Use – and elaborate – your competences and experience
  • Work in an interactive, flexible and positive working environment

Location:

This position is located at our office in Munich.

Contact:

For more information, please contact Dr. Michaele Kupka, Team Manager CRAs & Project Manager at +49 89 895286-0

Applications should be sent tojob@klifo.com marked “CRA, Munich”.

KLIFO processes your application and all related personal data exclusively for the specific hiring process. Your data is processed as confidential information, cf. the current data protection law (GDPR).

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