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Senior Clinical Research Associate

hace 2 meses


Madrid Centro, Madrid, España Worldwide Clinical Trials A tiempo completo

About Us

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

Our company's scientific heritage is anchored in our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases. We develop flexible plans and solve problems quickly for our customers, leveraging our talented team of 3,000+ professionals spanning 60+ countries.

Our Mission

We are united in our mission to improve the lives of patients through new and innovative therapies. We believe that everyone plays a vital 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.

Our Values

We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

What We Do

Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial.

Your 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, and review study subject safety information and informed consent and study material (e.g., CRFs, manuals).

What We're Looking For

  • 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.

Your Background

  • 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.).

Ability to meet the travel requirements of the job.