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Precision for Medicine

Clinical Research Associate I/ Clinical Research Associate II

УдалённоFrance только
Опубликовано
Роль
Исследования
Опыт
Джуниор
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Коротко по делу

Clinical Research Associate I/II based in Paris or Paris area, working remotely with site monitoring travel across France. Requires 1+ year CRA or equivalent clinical research experience, oncology study experience, life science degree or equivalent, and fluency in English plus French.

Обязательные навыки

ICH-GCP

Обязательные языки

English Fluent; application in English required.French Fluent/local language of country where position based

Чем предстоит заниматься

  • 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.

Что требуется

  • 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.

Преимущества

  • 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.
  • Influence and impact in a smaller CRO.
  • Support from direct line management.

Clinical Research

HealthcareКрупнаяprecisionformedicine.com/

Что говорят о компании

2.8/ 5

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