Clinical Research Associate II Specialist

hace 3 días


Málaga, Málaga, España Pharmiweb A tiempo completo

Parexel is a leading biopharmaceutical services provider that transforms scientific discoveries into new treatments. Our suite of services spans clinical trials, regulatory, consulting, and market access, backed by a strong commitment to our values: Patients First, Quality, Respect, Empowerment & Accountability.

In Spain, we're seeking a Clinical Research Associate II to join our Clinical Operations Team in Madrid or Barcelona. This role offers the opportunity to go beyond traditional clinical monitoring, with a focus on building and maintaining site relationships and ensuring their success.

As the sole point of contact for clinical sites, you'll address and resolve site issues and questions, manage site quality and delivery from identification through close-out, and leverage your expertise to promote rapport with site staff.

You'll also review performance at designated sites, safeguard human subject rights and well-being, and ensure compliance with protocols, SOPs, GCP, and applicable regulations.

We offer world-class technology and training tailored to your experience, reduced travel, and a lower protocol load compared to industry peers.

Your hard work may be rewarded through a bonus incentive program, opportunities to work across multiple therapeutic areas, and career advancement in clinical research.

If impact, flexibility, and career development appeal to you, Parexel could be your next home.

Key Responsibilities:
  • Leverage your expertise to conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites.
  • Build relationships with site staff and oversee the integrity of studies.
  • Protect patients' rights and well-being, ensuring compliance with protocols and regulations.
  • Drive productivity by developing patient recruitment strategies in conjunction with clinical sites.
  • Evaluate the quality and integrity of reported data, site efficacy, and drug accountability.
About You:

On your first day, we expect you to have:

  • Site management or equivalent experience in clinical research, with a solid 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 another health-related discipline.

Estimated Salary: €55,000 - €65,000 per annum, depending on location and experience.



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