Site Management Specialist

Há 5 dias


Lisboa, Lisboa, Portugal Merck Gruppe - Msd Sharp & Dohme Tempo inteiro

**Job Summary**

We are seeking a highly skilled Site Management Specialist to join our team. As a key member of our clinical operations group, you will be responsible for ensuring the smooth conduct of clinical trials at our partner sites. This includes developing and maintaining strong relationships with site personnel, ensuring compliance with study protocols, and identifying and resolving any issues that may arise during the trial.

**Responsibilities**

  • Develop and maintain relationships with site personnel to ensure effective communication and collaboration
  • Conduct regular on-site monitoring visits to verify data accuracy and ensure compliance with study protocols
  • Coordinate and manage tasks with sponsor roles to achieve Site Ready status
  • Participate in site selection and validation activities

**Requirements**

  • Bachelor's degree in a relevant field (e.g., life sciences, nursing)
  • Fluency in English (verbal and written) and excellent communication skills
  • Good understanding of GCP/ICH and country-specific clinical research laws and guidelines
  • Ability to present technical information effectively

**What We Offer**

We offer a competitive salary, comprehensive benefits package, and opportunities for professional growth and development. Our team is passionate about making a difference in people's lives, and we're looking for like-minded individuals to join us.


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