Senior Clinical Research Associate

Added
1 minute ago
Type
Full time
Salary
Salary not provided

Related skills

travel gcp monitoring dermatology site management

πŸ“‹ Description

  • Keep abreast of scientific, regulatory, and operational aspects.
  • Site evaluation and initiation visits; ensure proper startup docs.
  • Train site staff in all study procedures.
  • Conduct monitoring visits and review CRFs for quality.
  • Perform source data verification and data query resolution.
  • Coordinate safety reporting (AEs/SAEs/SUSARs) and follow-up.

🎯 Requirements

  • University degree in scientific, medical or paramedical disciplines.
  • Proven CRA with on-site monitoring experience.
  • Dermatology study experience.
  • Knowledge of GCP/ICH and regulatory requirements.
  • Fluent in English and local language(s).
  • Proficiency in Microsoft Office; willing to travel.

🎁 Benefits

  • Global CRO with focus on quality and development.
  • Training and professional development.
  • Equal opportunity employer with diverse culture.
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