GCP-Service is an independent full-service Clinical Research Organization which offers his clinical research services throughout Europe using the latest modern technologies. Since our foundation in 2004, the company has continuously grown enabling us to deliver the entire spectrum of services required for a successful conduct of clinical trials.

We love what we do and are convinced that our multiple innovative processes as well as our competences and continuous development of our employees provide unique advantages to our company, clients, partners and vendors.


Senior Clinical Research Associate (SCRA) in our Potsdam office (m/w/d)

GCP-Service International is a mid-size full service Clinical Research Organization based in Bremen Germany. Our satellite offices include locations in Potsdam, Siegburg, Netherlands, Poland, and Prague. We conduct a wide range of clinical trials in both the pharmaceutical and medical device industries all over the world.

We are a dynamic team looking for people who share our company values:

✓ Respect, acceptance and tolerance are the basis of a positive working environment
✓ We think that trust builds sustainability, stability and creativity
✓ We reach a high grade of satisfaction by our flexibility
✓ Reliability must be the basis of a service provider
✓ Fair and honest interactions are the basis of our interpersonal relationships
✓ Continuous professional and personal development enables us to achieve and exceed expectations

Working hours: Full-Time
Job Location: Potsdam

Core responsibilities:

  • Performing monitoring functions, like monitoring visits and follow up to assess the progress of clinical studies at assigned investigative sites (either on site or remotely) to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements
  • Managing and training of site personnel on protocol requirements, appropriate source documentation, and case report form completion.
  • Conducting site feasibility and maintaining contact with each assigned investigative site.

Your profile:

  • You should have approximately 3-5 years of clinical research experience
  • BA/BS degree in science/health care field or nursing degree or equivalent combined education and experience
  • Fluent in German and English all in speaking and writing.
  • Excellent communication and presentation skills
  • Understanding of corporate policies and procedures as well as ICH/GCP Guidelines and the national laws and regulations
  • Demonstrate an ability to prioritize and manage time for the preparation, completion and follow up of monitoring tasks.
  • Ability to manage up to 50% travel work time throughout Germany and Europe.

We are looking for talented people who are proactive and love to work with modern software. If you have the desire to begin an exciting career and the passion to support us in the development of useful medicinal products and medical devices, please contact us today!

If you are interested, send us your application with your salary expectations (salary will depend on your experience and performance), earliest start date, a cover letter and your CV to:

Judith Hüllebrand
GCP-Service International Ltd. & Co.KG
Friedrich-Ebert-Str. 57
14469 Potsdam, Germany
Phone: +49 (0) 331 -585-69-161