We are looking for a motivated Clinical research Associate fluent in English for a full-time or part-time position.

SCIRENT was founded in 2012 with the vision of helping customers develop innovative medical drugs and devices for patients with cardiovascular diseases. Our dedicated team of experienced clinical and regulatory professionals share their enthusiasm for developing effective therapies for cardiac patients. Our profound expertise in cardiovascular therapy and diagnostics sets us apart from our competitors. Our CRO offers access to an impeccable network of dedicated trial centers in Europe and North America with extensive experience in cardiovascular studies. Our customers appreciate our lean and agile management, which generally makes our performance faster and more efficient.

Your area of responsibility

  • Continuously review source data and ensure accurate and timely reporting and follow-up of Adverse Events (AE)/Serious Adverse Events (SAE)
  • Support study sites with accurate documentation related to clinical data, relevant training, protocol deviations, etc.
  • Prepare, conduct and report on activities related to site qualification, initiation, clinical surveillance and final visits
  • Ensuring the proper handling, accountability, and reconciliation of investigational devices and other clinical trial materials
  • Assists the regulatory team with local filings and EC/RA communications where applicable
  • Escalates appropriately and timely to the project manager
  • Site - Qualifications

Your profile

  • Excellent team player, problem solving, positive attitude and ability to take initiative
  • Bachelor's degree or its international equivalent in a clinical, scientific or health-related field from an accredited institution
  • Read, write and speak English and knowledge of medical language
  • ICH/GCP training certificates according to local guidelines
  • You have already worked as a CRA for at least two years and are qualified to sign documents independently
  • Ability to work both independently and on a team, contributing own ideas
  • Organizational talent


Onboarding: Welcome trips to our partner countries, newcomers meet & greet - we ensure your perfect start

Training: Your development is important to us. We offer in-house training in all areas of clinical research. There is the possibility of voluntary language courses or regular coaching - we will keep you updated!

Flexibility: With flexible working hours and mobile office.

Accessibility: Our modern office right in the heart of Berlin is easy to reach thanks to its perfect location

Internationality: As an internationally group, we offer you the opportunity to network and exchange ideas with colleagues from a wide variety of disciplines from all over the world

We are looking forward to receiving your complete application documents, stating the possible start of work.

CEO: Prof. Dr. med. Hans-Dirk Düngen

SCIRENT Clinical Research and Science

Amrumer Str. 16, 13353 Berlin

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If you experience any problems with the form above please send your application directly to: contact.berlin@scirent.com

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