Senior Clinical Research Associate - Remote EU Role

Arbeitnow

France

Hybride

EUR 65 000 - 85 000

Plein temps

Il y a 13 jours
Générateur de candidature

Une candidature sur mesure pour ce poste — un CV personnalisé et une lettre de motivation qui correspondent directement à l’offre.

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Résumé du poste

Precision for Medicine is seeking Senior Clinical Research Associates to support a dedicated FSP partnership across Poland, Hungary, the UK, France and Germany. The role can be fully home-based within France and involves substantial travel to coordinate regulatory submissions, site initiation visits, and study monitoring.

You will work with clients to ensure studies are conducted per protocol and ICH-GCP, while mentoring junior staff and contributing to proposals.

Qualifications

  • Minimum 5 years of CRA/ SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
  • Experience monitoring clinical trials across a variety of therapeutic areas
  • Availability for domestic travel including overnight stays, up to 50–60% travel commitment (international travel may be required)
  • Fluency in English and the local language is required

Responsabilités

  • Monitor and own the progress of clinical studies at investigative sites and ensure trials are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations
  • Coordinate activities to set up and monitor a study (identify investigators; help prepare regulatory submissions; conduct pre-study and initiation visits)
  • Train and mentor junior staff; interact with clients; initiate payments; participate in proposal activities

Connaissances

English fluency
Local language fluency

Formation

4-year college degree or equivalent
CRA certificate
Graduate/postgraduate degree (preferred)

Description du poste

Precision for Medicine is seeking Senior Clinical Research Associates to support a dedicated FSP partnership across Poland, Hungary, the UK, France and Germany. The role can be fully home-based within France and involves substantial travel to coordinate regulatory submissions, site initiation visits, and study monitoring.

You will work with clients to ensure studies are conducted per protocol and ICH-GCP, while mentoring junior staff and contributing to proposals.

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