Clinical Trial Coordinator

Há 8 horas

São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$48.000 - R$72.000

As a Research Monitoring Associate, you will be responsible for ensuring the integrity of clinical trials by conducting site visits and reviewing data accuracy.

Key Responsibilities
  • Monitor trial sites to ensure compliance with protocol requirements and regulatory standards.
  • Assess investigational product quality through physical inventory and records review.
  • Document observations in reports and letters using approved business writing standards.
  • Evaluate and escalate observed deficiencies and issues to clinical management promptly.
  • Maintain regular contact with investigative sites between monitoring visits to confirm protocol adherence and resolve identified issues.
Additional Responsibilities
  • Participate in investigator meetings and identify potential investigators in collaboration with client companies.
  • Initiate clinical trial sites according to relevant procedures to ensure compliance with protocols and regulatory requirements.
  • Perform trial close-out and retrieval of trial materials.
  • Ensure essential documents are complete and in place according to ICH-GCP and applicable regulations.
Requirements
  • Bachelor's degree in a life sciences-related field or equivalent qualification.
  • Minimal clinical monitoring experience (comparable to 2 years) in a clinical environment.
  • Valid driver's license where applicable.
Skill Requirements
  • Basic medical/therapeutic area knowledge and understanding of medical terminology.
  • Ability to attain and maintain a working knowledge of ICH GCPs and applicable regulations.
  • Good oral and written communication skills.
  • Good interpersonal skills.

The ideal candidate will have strong analytical skills, attention to detail, and excellent communication skills. They must also be able to work independently and as part of a team.

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