Clinical Research Associate

hace 7 días


Madrid, Madrid, España Worldwide Clinical Trials A tiempo completo

Requisition Number

6651

Employment Type:

Regular

_ Are looking to become a CRA?_

Who we are


We're a global, midsize CRO that pushes boundaries, innovates, and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe.

It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

What you will do


Our entry-level program, The CRA Academy, is designed to provide the foundational clinical research training to become a CRA I.

Employees in The CRA Academy participate in a 5-month training program.


The first 12 weeks consist of virtual classroom training which includes ILT, role-playing, group discussions, case studies, self-paced learning, homework assignments, and knowledge checks.

The program content will cover a dive into the clinical research industry and will focus specifically on how this all ties into the CRA's role and responsibilities.

You will also receive training on Worldwide's specific processes and frequently used systems. We expect all to be active participants in this learning process.


Starting at approximately your 6th week, you will have opportunity to attend site visits with experienced, trained CRA mentors for on-the-job training.


We will utilize a see one:

do one:
teach one approach during these training.


The CRA Academy plays 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 help drive breakthrough scientific research and playing a lead role in every clinical trial. All CROs will promise you growth, opportunity, and maybe even a challenge. But we offer more than that. We offer an uncommon experience - one you can't get anywhere else, with a team unlike anyone else.

What you will bring to the role

  • Excellent planning and organizational skills with effective time management
  • Ability to work in an organized and methodical manner, both independently and as a team member
  • Strong attention to detail and focus on quality work
  • Good understanding of standard operating procedures
  • Ability to work in a fastpaced environment and to comply with regulatory requirements and deadlines

Your experience

  • Experience working in Clinical Research is desired
  • Bachelor's degree or equivalent with a major concentration in medical, biological, physical, health, pharmacy, or other related science is required
  • Willingness to travel at least 60% required
  • Valid current passport and driving license required
  • Fluent in the local language of the country under responsibility and proficient in both spoken and written English

Why Worldwide
At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up.

We empower our team members to treat every clinical trial like a patient's life depends on it - because it does.

Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

  • Worldwide Conducts a background verification which includes verification of education and previous employment._
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