Senior CRA – Home-Based, Impactful Oncology Role

Precision for Medicine

United States

A distancia

USD 56.000 - 83.000

Jornada completa

Hace 11 días

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Descripción de la vacante

Precision for Medicine in the United Kingdom is hiring a Senior Clinical Research Associate/CRA II for a fully home-based role in the UK or Northern Ireland. This position offers the opportunity to manage studies remotely while contributing to high-quality oncology trials and benefiting from a collaborative, people-focused culture.

You will monitor sites, ensure adherence to protocol and ICH-GCP standards, and coordinate regulatory submissions, initiation visits, and investigator meetings.

Formación

  • 4-year college degree or equivalent experience.
  • Candidates should ideally have more than 1 year CRA experience within the CRO or pharmaceutical industry.
  • Oncology experience desirable.
  • Availability for domestic travel including overnight stays, which may be up to 50-60% travel commitment (international travel may be required for some senior level positions).
  • Fluency in English.

Responsabilidades

  • Monitor and own the progress of clinical studies at investigative sites and ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations and standards.
  • Coordinate activities required to set up and monitor a study (e.g., identify investigators; help prepare regulatory submissions; conduct pre-study and initiation visits).

Conocimientos

Fluency in English

Educación

4-year college degree or equivalent

Descripción del empleo

Precision for Medicine in the United Kingdom is hiring a Senior Clinical Research Associate/CRA II for a fully home-based role in the UK or Northern Ireland. This position offers the opportunity to manage studies remotely while contributing to high-quality oncology trials and benefiting from a collaborative, people-focused culture.

You will monitor sites, ensure adherence to protocol and ICH-GCP standards, and coordinate regulatory submissions, initiation visits, and investigator meetings.

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