Biopharmaceutical Research Professional

hace 2 semanas


Madrid, Madrid, España Parexel A tiempo completo
About Parexel

Parexel is a global biopharmaceutical services company dedicated to improving the world's health. We achieve this by providing a range of services that help clients across the globe transform scientific discoveries into new treatments.

Job Overview

We are currently seeking a Clinical Research Associate II to join our Clinical Operations Team in Spain. This role can be based in Madrid or decentralized in the regions of Madrid or Barcelona.

About the Job

This position offers the opportunity to go beyond the typical clinical monitoring role. As a CRA, you will be accountable for building and maintaining site relationships and ensuring they are set up for success. You will manage site quality and delivery from site identification through to close-out.

Duties and Responsibilities
  • Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites and generate visit/contact reports.
  • Build relationships with site staff and oversee the integrity of the study.
  • Protect patient rights and well-being by reviewing the performance of the trial at designated sites.
  • Develop patient recruitment strategies with clinical sites to meet enrollment timelines.
  • Evaluate the quality and integrity of reported data, site efficacy, and drug accountability.
  • Monitor the completeness and quality of regulatory documentation and perform site document verification.
Requirements

To be successful in this role, you should have:

  • Site management or equivalent experience in clinical research with understanding of clinical trials methodology and terminology.
  • The ability to perform all clinical monitoring activities independently.
  • A bachelor's degree in biological science, pharmacy, or other health-related discipline.
  • Strong interpersonal, written, and verbal communication skills within a matrixed team.
  • Fluent knowledge of Spanish and English languages.
  • Experience working in a self-driven capacity with limited oversight.
  • A client-focused approach to work and flexible attitude with respect to assignments/new learning.
  • The ability to manage multiple tasks and achieve project timelines.
  • An honest and ethical work approach to promote the development of life-changing treatments for patients.
  • Strong computer skills including knowledge of clinical trial management systems, electronic document management systems, and MS-Office products.
Salary and Benefits

The estimated annual salary for this position is $70,000-$90,000 depending on location and experience. Additionally, you may be eligible for a bonus incentive program, career development opportunities, and a range of benefits to support your personal and professional growth.



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