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Precision for Medicine

Clinical Research Associate I/ Clinical Research Associate II

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

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

No BS summary

CRA I/II based in Paris or the Paris area, with 1+ year CRA or equivalent clinical research experience. Must have oncology study experience, site management experience, English and French fluency, and be available for domestic travel up to 50–60%.

Required skills

ICH-GCP

Required languages

English Fluent / apply in English; requiredFrench Fluent; required local language of country where position based

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.
  • Identify investigators.
  • Help prepare regulatory submissions.
  • Conduct pre-study and initiation visits.

What they require

  • Life science degree and / or equivalent experience.
  • 1 year or more 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.
  • Experience managing oncology studies.
  • Availability for domestic travel including overnight stays, as required; international travel may be required for some senior level positions.
  • 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 for non-English speaking countries the local language of country where position based.
  • Preferred: Study start up activities experience.
  • Please apply in English.

Benefits

  • Lower than average number of protocols, 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.
  • Support from direct line management.

Clinical Research

HealthcareEnterpriseprecisionformedicine.com/

What people say about this company

2.8/ 5

Details

Apply routeGreenhouse
Salary not disclosed