Similar Jobs

See all

About the Role:

  • Monitor clinical studies at sites, ensuring compliance with protocols, SOPs, and ICH-GCP.
  • Coordinate study setup, including investigator identification and regulatory submissions.

Qualifications:

  • Minimum 5 years of CRA/SCRA experience in CRO, pharma, biotech, or medical device.
  • Fluency in English and local language required; additional languages a plus.

Working at Precision:

  • Collaborate with a dedicated sponsor in a quality-focused environment.
  • Enjoy a home-based role in France with travel expectations.

Opportunities for Growth:

  • Train and mentor junior staff.
  • Engage in proposal activities and client presentations.

Precision for Medicine

Precision for Medicine is a specialized CRO that combines agility with scientific expertise to support innovative clinical development programs. They foster a collaborative environment that values quality, accountability, and professional development, with a global team of experienced professionals.

Apply for This Position