Director Of Clinical Research Operations

confidential; São Paulo; Presencial; BRL 160.000 - 200.000; Tempo integral

Resumo da oferta

A leading healthcare organization in São Paulo is seeking a Director of Clinical Research Operations to lead clinical research with a strategic focus on excellence and compliance. This senior role requires strong leadership and relationship-building skills, ensuring integration across teams and stakeholders during clinical studies. Candidates should have a degree in health sciences or similar fields, along with over 10 years of relevant experience in clinical operations.

Qualificações

• Minimum of 10 years of experience in managing clinical research studies.
• Solid background in clinical operations and strategic leadership.
• Strong understanding of national and international regulations.

Responsabilidades

• Define and implement the operational strategy for clinical studies.
• Ensure quality, timelines, and full compliance with ICH-GCP, ANVISA, and international standards.
• Lead, inspire, and develop multidisciplinary teams.
• Drive continuous improvement and monitor performance indicators (KPIs).
• Manage contracts and partnerships with sponsors, CROs, research sites, and vendors.
• Represent the organization in industry forums and professional events.
• Assess study feasibility and optimize resource allocation.

Conhecimentos

Leadership

Compliance

Relationship building

Strategic mindset

Continuous improvement

Formação académica

Degree in Health Sciences, Pharmacy, Biomedical Sciences or related fields

Postgraduate degree/MBA

Descrição da oferta de emprego

Director of Clinical Research Operations

We are seeking a senior professional to lead the clinical research operations with a strategic mindset and a focus on excellence, compliance, and efficiency.

This role requires strong leadership and relationship‑building skills, ensuring full integration across teams, stakeholders, and sponsors throughout all phases of clinical studies.

Key Responsibilities

• Define and implement the operational strategy for clinical studies.
• Ensure quality, timelines, and full compliance with ICH‑GCP, ANVISA, and international standards.
• Lead, inspire, and develop multidisciplinary teams.
• Drive continuous improvement and monitor performance indicators (KPIs).
• Manage contracts and partnerships with sponsors, CROs, research sites, and vendors.
• Represent the organization in industry forums and professional events.
• Assess study feasibility and optimize resource allocation.

Requirements

• Degree in Health Sciences, Pharmacy, Biomedical Sciences, or related fields.
• Postgraduate degree/MBA in Management, Clinical Research, or related areas.
• Solid background in clinical operations and strategic leadership.
• Strong understanding of national and international regulations.
• Minimum of 10 years of experience in managing clinical research studies.