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Clinical Research Associate II

3 hours, 16 minutes ago
Spain
Full-time
Junior
Operations Specialist
Operations
Apply Now
Precision Medicine Group

Precision Medicine Group

Precision Medicine Group specializes in precision medicine, utilizing targeted expertise and data insights to accelerate drug development and enhance the commercialization of next-generation medical products for the pharmaceutical and life sciences ind...

Pharmaceuticals
251-1K
Founded 2012
View All Jobs 147

Description

  • Monitor and own the progress of clinical studies at investigative sites.
  • Ensure studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, and applicable regulations and standards.
  • Coordinate study start-up and monitoring activities, including identifying investigators.
  • Support preparation of regulatory submissions.
  • Conduct pre-study visits and site initiation visits.
  • Identify potential study risks and propose mitigation strategies.
  • Manage site-level issues and handle conflict using effective resolution approaches.
  • Maintain high quality and accountability for study outcomes.
  • Collaborate with project teams and provide updates as needed.

Requirements

  • 4-year college degree or equivalent experience.
  • 2+ years of experience as a CRA in a CRO or pharmaceutical/biotech environment, or equivalent relevant experience.
  • Site management experience or equivalent experience in clinical research.
  • Oncology monitoring experience.
  • Availability for domestic travel, including overnight stays, up to approximately 50-60%.
  • Fluency in English and, for non-English speaking countries, the local language of the country where the position is based.
  • Must reside in Madrid or Barcelona.
  • Graduate or postgraduate degree in a scientific or healthcare discipline preferred.

Benefits

  • High CRA retention and a supportive team culture.
  • Lower-than-average protocol load to help you become a protocol expert.
  • Reasonable travel expectations that support work-life balance.
  • Opportunity to have a visible voice and real influence in a smaller CRO.
  • Support from direct line management.
  • Meaningful impact on oncology and rare disease clinical development.
  • Employees’ ideas are valued and nurtured.
  • Remote-friendly posting indicated by #LI-Remote.

Interested in this position?

Apply directly on the company website

Apply Now

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