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Senior Clinical Research Associate

hace 2 meses

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

We are seeking a highly skilled Clinical Research Associate to join our team at Worldwide Clinical Trials, LLC. As a key member of our Clinical Operations team, you will play a vital role in ensuring the success of our clinical research programs.

Key Responsibilities
  • Conduct site qualifications, initiation, interim monitoring, site management, and study close-out visits to ensure compliance and quality.
  • Review study subject safety information and informed consent, and conduct source document verification to ensure accuracy and completeness.
  • Participate in study team and investigator meetings to discuss trial progress and address any concerns.
  • 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 detail.
  • Broad understanding of clinical research principles and processes.
  • 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.
  • Ability to meet the travel requirements of the job.
About Us

Worldwide Clinical Trials, LLC is a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to reality.