We love what we do and our business is growing continuously.
Due to the continuous growth we always need good people in different operational working areas of our company. However, our aim is to be the best CRO proving the best services to our clients.
For this reason we only need the best people.


Our Biostatistician support our Clinical Data Management department according to Standard Operating Procedures (SOPs) of GCP-Service or Sponsor, ICH/GCP Guidelines and the national laws and regulations. In this role, you will provide comprehensive biostatistical support for all relevant fields.

The successful candidate will manage the delivery of high quality data from project start-up and planning to project execution and project closeout on several projects.You will independently perform project specific quality control and quality assurance tasks on all projects responsible for, as well as other projects, when requested.

Duties and Responsibilities:

  • Ensure consistency, accuracy, and adherence to federal regulations, Good Clinical Practice, Good Clinical Data Management Practices, as well as SOPs and Working Instructions.
  • Contribute to development and maintenance of statistic guidelines and SOPs according to the international quality standards and legislations.
  • Involved in statistical tasks related to clinical trials, e.g. conducting sample size calculations, writing Statistical Analysis Plans (SAPs), preparation of Tables, Figures and Listings (TFLs)
  • Maintain client communication regarding statistic project status and review key project questions with clients.

Required Qualifications:

  • Master level degree in Mathematics, Biostatistics, Statistics, Computer Sciences or equivalent qualification. Relevant work experience is desired.
  • Programming experience (SAS knowledge desired)
  • Microsoft office product experience
  • Organizational, communication and computer skills
  • Fluent in English and German, written and spoken

Preferred Experience.

  • Ideally experience in statistical tasks for clinical trials
  • Experience in statistical methods gained in previous position
  • Other programming experience in e.g. R

If you are interested, send us your electronic application (with your salary expectations and earliest start date) and your CV to:

Thomas Kissner
GCP-Service International Ltd. & Co.KG
Anne-Conway-Str. 2
28359 Bremen
Phone: +49 (0) 421 89676612
Fax: +49 (0) 421 4348659