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Precision for Medicine

Clinical Research Associate

УдалённоGermany только
Опубликовано
Роль
Исследования
Опыт
Джуниор
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Доступно для: DE only. Укажите, откуда вы работаете, чтобы проверить доступность.

Коротко по делу

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%.

Ключевые навыки

Clinical monitoring

Обязательные навыки

ICH-GCP

Обязательные языки

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

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, including identifying investigators, helping prepare regulatory submissions, and conducting pre-study and initiation visits.

Что требуется

  • 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.

Преимущества

  • 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

HealthcareКрупнаяprecisionformedicine.com/

Что говорят о компании

2.8/ 5

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