Senior Clinical Research Associate

hace 7 días

Barcelona, Barcelona, España Worldwide Clinical Trials, Llc A tiempo completo

Clinical Operations Site Management

At Worldwide Clinical Trials, LLC, we are seeking a highly skilled Clinical Operations Site Management professional to join our team. As a key member of our clinical research operations team, you will play a vital role in ensuring the successful execution of our clinical research programs.

Key Responsibilities:

  • Conduct 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 data veracity
  • 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 detail
  • Broad understanding of clinical research principles and processes
  • Proficiency in Microsoft Office, CTMS, and EDC Systems
  • 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. We are united in our cause to improve the lives of patients through new and innovative therapies.

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