Clinical Research Site Manager

vor 2 Wochen


Schweiz Merck Sharp & Dohme (MSD) Vollzeit
Job Summary

We are seeking a highly skilled and experienced Site Executive, GCTO to join our team at Merck Sharp & Dohme (MSD). As a key member of our clinical research team, you will be responsible for ensuring the successful execution of clinical trials at assigned sites in China.

Key Responsibilities
  • Develop and maintain strong relationships with site investigators and staff to ensure compliance with ICH-GCP, Sponsor SOPs, and local regulations.
  • Conduct site visits, including initiation, monitoring, and close-out visits, to ensure data quality and subject safety.
  • Collaborate with internal stakeholders, including CRA Manager, CRM, and TA Head, to resolve site performance and quality issues.
  • Manage and maintain site documentation, including CTMS and eTMF, to ensure compliance and data integrity.
  • Contribute to the development and implementation of site selection and validation strategies.
  • Participate in internal meetings and workstreams as a subject matter expert on monitoring processes and systems.
Requirements
  • Strong understanding of ICH-GCP, Sponsor SOPs, and local regulations.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Strong problem-solving and analytical skills.
  • Proficiency in CTMS and eTMF systems.
What We Offer
  • Competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • Collaborative and dynamic work environment.


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