Senior Clinical Trial Manager

Há 2 dias

Santo Amaro, Bahia, Brasil beBeeClinical Tempo inteiro R$90.000 - R$120.000
Job Summary

The role involves planning, executing, and interpreting clinical trials research, data collection activities, and clinical operations. Collaboration with investigational sites, clinical consultants, Contract Research Organizations & vendors is required. This position directs activities to execute and deliver assigned studies, ensuring adherence to research protocols, regulatory requirements, and good clinical practices.

Key responsibilities include:

  • Liaising between stakeholders to ensure successful collaboration and meeting expectations on milestones and deliverables.
  • Managing assigned study sites, conducting phase I-IV protocols according to the Monitoring Plan and established procedures.
  • Performing site initiation visits, training site personnel, and re-training as necessary.
  • Conducting continuous site monitoring activities (onsite and remote) to ensure compliance with protocol, ICH/GCP, global and local regulations.
  • Identifying deficiencies in site processes and collaborating with sites on risk mitigation and process improvements.

This role promotes a compliance culture, advocating adherence to highest standards and ethical integrity, ensuring human subject protection and reliability of trial results at all times.

Requirements

To be considered for this role, you should have:

  • A minimum 5 years pharmaceutical industry experience in all aspects of monitoring and site management.
  • Experience in operations management, project management, people leadership, and collaboration across boundaries.

Additionally, strong skills in communication, influencing others, relationship management, digital capabilities, analytical thinking, and problem-solving are essential.

Languages

Candidate should be proficient in English language.

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