Director of Clinical Research Operations

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

Resumo da oferta

A leading clinical research organization in São Paulo seeks a Director of Clinical Research Operations to lead clinical operations with a focus on excellence and compliance. Candidates should have over 10 years of experience, strong leadership skills, and a strategic mindset. This full-time role requires managing multidisciplinary teams and ensuring compliance with international standards.

Qualificações

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

Relationship-building

Strategic mindset

Compliance knowledge

Performance monitoring

Formação académica

Degree in Health Sciences, Pharmacy, Biomedical Sciences

Postgraduate degree/MBA

Descrição da oferta de emprego

Director of Clinical Research Operations

BRL 160.000 - 200.000

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.

Seniority level

Director

Employment type

Full-time

Job function

Strategy/Planning and Project Management