Clinical Trials Site Manager

Há 5 dias

São Paulo, São Paulo, Brasil beBeeSiteManagement Tempo inteiro US$60.000 - US$75.000

We are seeking a seasoned Site Management Specialist to join our team. This key role will oversee the coordination of clinical trials, ensuring seamless execution and adherence to regulatory guidelines.

Key Responsibilities:

  • Act as primary local company contact for assigned sites
  • Participate in site feasibility assessments and qualification visits
  • Attend investigator meetings, prepare meeting materials, and present at IMs as needed
  • Execute activities within site initiation and start-up, preparation and conduct of site monitoring, site management, and site/study close-out according to SOPs and policies

The ideal candidate will possess a strong working knowledge of GCP, company SOPs, local laws and regulations, assigned protocols, and associated protocol-specific procedures. They will also have excellent communication skills, both written and verbal, and be proficient in using relevant software and systems.

Benefits:

  • Ongoing training and professional development opportunities
  • A dynamic and supportive work environment
  • The chance to work on multiple trials in parallel

If you are a motivated and organized individual with a passion for clinical trial management, we encourage you to apply for this exciting opportunity.

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