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Precision for Medicine

Clinical Research Associate

RemoteGermany only
Published
Role
Research
Experience
Junior
Salary not disclosed
Check eligibility

Open to DE only. Set where you work from to check your eligibility.

No BS summary

Clinical Research Associate in Germany with at least 1 year of CRA experience in CRO, pharma/biotech, or equivalent clinical research site management experience. Must be fluent in English and German, have oncology experience, and be available for domestic travel up to approximately 50–60%.

Core skills

Clinical monitoring

Required skills

ICH-GCP

Required languages

English Fluent / apply in English required statewide by posting; exact level stated as Fluency.German Fluent

What you'll do

  • Monitor and own the progress of clinical studies at investigative sites.
  • Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
  • Coordinate all necessary activities required to set up and monitor a study, including identifying investigators, helping prepare regulatory submissions, and conducting pre-study and initiation visits.

What they require

  • Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline.
  • At least one year as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies.
  • Site management or equivalent experience in clinical research.
  • Excellent communication and organizational skills are essential.
  • A team player.
  • Evidence of a client focused approach.
  • Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment.
  • International travel may be required for some senior level positions.
  • Fluency in English and German.
  • Experience in oncology.
  • Preferred: Study start up activities experience.
  • Preferred: CAR-T or FIH studies - phase III.
  • Preferred: Medical device experience.
  • Please, apply in English.

Benefits

  • Extremely high CRA retention rates compared to industry averages.
  • Focus on an average of one to two studies, setting you up to be a protocol expert.
  • Reasonable travel and improved work/life balance.
  • Your voice will be heard.
  • Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.
  • You will provide input and have your ideas valued and nurtured, impacting positive change for the company.

Clinical Research

HealthcareEnterpriseprecisionformedicine.com/

What people say about this company

2.8/ 5

Salary not disclosed