Clinical Research Operations Coordinator

hace 2 semanas

Sant Cugat, Barcelona, España Grifols A tiempo completo

Are you interested in becoming part of a global team dedicated to advancing healthcare solutions? At Grifols, a pioneering healthcare organization established in 1909, we are committed to enhancing the health and well-being of individuals worldwide. As leaders in the field of plasma-derived therapies and transfusion medicine, we develop, manufacture, and distribute innovative medical products and services across over 110 countries.

Our commitment to diversity enriches our workforce and corporate culture, fostering an inclusive environment for all.

We are currently seeking a Clinical Research Operations Coordinator within our Clinical Operations department. This role is essential for ensuring the effective execution of clinical trials for our Bioscience portfolio, adhering to ICH-GCP standards and relevant regulatory frameworks.

Key Responsibilities

  • Collaborate with the Clinical Operations Manager to align departmental objectives with organizational goals.
  • Enhance and optimize Clinical Operations workflows to boost efficiency and uphold quality benchmarks.
  • Engage with various functional teams to identify, assess, and refine cross-functional processes throughout clinical initiatives.
  • Provide support to Clinical Operations personnel and project teams, offering guidance to address compliance challenges.
  • Participate in the development and implementation of innovative technologies within the Clinical Operations sector.
  • Ensure adherence to GCP/ICH and regulatory standards.

Candidate Profile

To excel in this position, candidates must demonstrate proficiency in the following areas:

  • A degree in Life Sciences or a related field, with a Master’s degree preferred.
  • A minimum of 3 years of experience in clinical trials, preferably as a site monitor or Clinical Research Associate (CRA).
  • Proficiency in both written and spoken English.
  • Familiarity with ICH GCPs, FDA, EMA, and CFR regulatory requirements, along with an understanding of the evolving regulatory landscape.
  • Knowledge of Clinical Operations processes, systems, and standard operating procedures (SOPs) essential for conducting clinical studies.
  • Strong communication skills and the ability to thrive in dynamic and flexible environments.
  • A keen attention to detail, coupled with excellent organizational and time-management capabilities.

What We Offer

This is an exceptional opportunity to join Grifols, where we recognize that our employees are our greatest asset. We are dedicated to fostering a workplace that promotes professional growth and development in a supportive environment.

For more information about Grifols, please visit our website. We look forward to your interest in this exciting opportunity.

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