Clinical Research Associate

medicomp/KLIFO is looking for a talented and committed Clinical Research Associate (CRA) for its office in Munich (Germany)

Since more than 33 years medicomp is offering its services as CRO and is very well established in the market.  Recently medicomp has been acquired by the Danish drug development consultancy KLIFO A/S (Glostrup, Denmark, and is now expanding its dynamic and experienced team. The people we want to engage like to work in a family-like environment and have a positive, proactive, flexible, self-driven and collaborative personality. We can offer a highly flexible, free and trustful working climate with exciting projects among competent colleagues where your contribution is valuable and makes a difference.

KLIFO and its German branch medicomp are service providers of drug development competences and operational services to the pharmaceutical, biotech and med-tech companies in Europe, US and Asia. The areas covered by us include Clinical Trial Supply, Clinical Trial Services, Pharmacovigilance, Regulatory Affairs and Drug Development Counselling.


The position as Clinical Research Associate:

The Clinical Research Associate (CRA) is responsible for the pro-active site management including monitoring activity of trials, i.e.:

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


The qualifications of the CRA:

The Clinical Research Associate should possess the following qualifications:

  • Sc. in the life sciences field or CRA specific diploma and a minimum of 2 years in a similar position in the pharmaceutical industry/BioTech/CRO
  • 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 or comparable level
  • Excellent computer skills, ability to develop and maintain excel spreadsheets and to elaborate PowerPoint presentations
  • Strong organizational skills with attention to details

In addition to the above-mentioned qualifications the ideal candidate is a dedicated and collaborative team player, possesses excellent planning skills and is 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

As medicomp is a smaller service provider, you will experience a high level of transparency, influence and a good possibility for individual planning with the advantage of being a part of a medium-sized, international integrated drug development consultancy via KLIFO A/S.



For more information, please contact Doris Wiegel, General Manager medicomp GmbH at +49 89 895286-0


Applications should be sent to; ed.orc-pmocidem@legeiw.sirod


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