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CRA II

ICON Strategic Solutions

España

A distancia

EUR 30.000 - 50.000

Jornada completa

Hoy
Sé de los primeros/as/es en solicitar esta vacante

Descripción de la vacante

A leading clinical research organization is looking for a Sr. Clinical Research Associate to conduct clinical trials in Madrid/Barcelona. The ideal candidate will have a Bachelor's degree, at least two years of experience, and strong knowledge of clinical trial processes. The role requires travel of up to 60%. Attractive benefits include health insurance and retirement planning.

Servicios

Various annual leave entitlements
Health insurance offerings
Competitive retirement planning
Employee assistance programme
Flexible optional benefits

Formación

  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of ICH-GCP guidelines.
  • Ability to travel at least 60% of the time.

Responsabilidades

  • Conduct site qualification, initiation, monitoring, and close-out visits.
  • Ensure protocol compliance, data integrity, and patient safety.
  • Prepare and review study documentation.

Conocimientos

Clinical trial processes
Regulatory knowledge
Strong communication skills
Organization skills

Educación

Bachelor's degree in a scientific or healthcare-related field
Descripción del empleo
Overview

Sr. Clinical Research Associate - Sponsor dedicated - Home Based Madrid/Barcelona

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

What you will be doing
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
Your profile
  • Bachelor\'s degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.
What ICON can offer you
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

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