Senior Clinical Research Associate

hace 1 mes


Zaragoza, Zaragoza, España Worldwide Clinical Trials A tiempo completo
Join Our Team at Worldwide Clinical Trials

We are a leading global contract research organization (CRO) working in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications. Our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases enables us to develop flexible plans and solve problems quickly for our customers.

Our Mission

We believe everyone plays an important role in making a world of difference for patients and their caregivers. Our hands-on, accessible leaders and cohesive, supportive teams are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity.

What We Do
  • 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, and compile and ensure completeness of regulatory documents and ethical submission documentation.
What We're Looking For
  • 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.
Requirements
  • 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.


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