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Senior Clinical Research Associate

hace 2 meses


Madrid, Madrid, España Worldwide Clinical Trials A tiempo completo
About the Role

As a Senior Clinical Research Associate - Clinical Operations Site Management at Worldwide Clinical Trials, you will play a vital role in ensuring the execution of our clinical research programs with the highest quality and excellence our sponsors expect.

Key Responsibilities
  • Conduct all types of visits, including site qualifications, initiation, interim monitoring, site management, and study close-out visits.
  • Review study subject safety information and informed consent, and conduct source document verification for compliance, patient safety, and veracity of data.
  • Actively participate in study team and investigator meetings.
  • Compile and ensure completeness of regulatory documents and ethical submission documentation.
Requirements
  • Excellent interpersonal, oral, and written communication skills in English and local language.
  • Superior organizational skills with attention to details.
  • Broad understanding of clinical research principles and process.
  • Proficiency in Microsoft Office, CTMS, and EDC Systems.
Education and Experience
  • Four-year college curriculum in life sciences, or
  • Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree) and one year experience with clinical research (e.g., study coordinator, CTA, etc.).
Travel Requirements

The ability to meet the travel requirements of the job is essential.