Clinical Trial Associate

BR03 (FCRS = BR003) NOVARTIS BIOCIENCIAS S.A; Santo Amaro; Presencial; BRL 60 000 - 82 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health insurance

Annual bonus

Life insurance

Flexible working arrangements

Birthday day-off

Parental leave

Subsidized dining facilities

Resumo da oferta

Novartis Biociências S.A. in Santo Amaro, Brazil, is seeking a Clinical Trial Associate to support start-up and delivery of global studies, ensuring sites are ready and compliant to advance groundbreaking research.

You will collaborate with investigators and cross‑functional teams, supporting regulatory submissions, trial master files, and study milestones while upholding GCP and Novartis standards.

Qualificações

• Bachelor's degree or equivalent in life sciences or related field.
• Experience supporting clinical trials or clinical operations in regulated environments.
• Understanding of clinical drug development and GCP requirements.

Responsabilidades

• Support study start-up activities and trial delivery through the full lifecycle.
• Prepare and manage essential regulatory and ethics submission documents.
• Maintain trial master files and ensure document quality and inspection readiness.
• Coordinate site activation activities and study drug release requirements.
• Collaborate with vendors, investigators, and cross-functional teams to meet milestones.
• Ensure compliance with regulatory requirements, GCP, and Novartis standards.
• Drive process improvements to enhance operational efficiency and execution.

Conhecimentos

Regulatory documentation

Clinical trials support

Communication & collaboration

Formação académica

Bachelor's degree in life sciences

Descrição da oferta de emprego

Job Description Summary

Location: Santo Amaro, Brazil

Relocation Support: This role is based in Santo Amaro, Brazil. Novartis is unable to offer relocation support: please only apply if accessible.

Are you passionate about bringing innovative medicines to patients faster? As a Clinical Trial Associate, you will play a vital role in the successful start-up and delivery of global clinical studies, helping ensure sites are ready, compliant, and equipped to advance groundbreaking research. Working closely with cross‑functional teams, investigators, and external partners, you will support critical study activities throughout the clinical trial lifecycle, making a direct impact on the quality, efficiency, and success of clinical development at Novartis.

Key Responsibilities

• Support study start‑up activities and clinical trial delivery throughout the full study lifecycle.
• Prepare, collect, and manage essential documentation for regulatory and ethics submissions.
• Maintain trial master files and ensure document quality, completeness, and inspection readiness.
• Coordinate site activation activities and verify requirements for study drug release.
• Collaborate with vendors, investigators, and cross‑functional teams to achieve study milestones.
• Ensure compliance with regulatory requirements, Good Clinical Practice, and Novartis standards.
• Drive process improvements that enhance operational efficiency and study execution.

Essential Requirements

• Bachelor's degree, vocational qualification, or equivalent education in a life sciences or related field.
• Experience supporting clinical trials or clinical operations within a regulated environment.
• Understanding of clinical drug development and study start‑up processes.
• Knowledge of Good Clinical Practice and regulatory requirements governing clinical research.
• Strong organisational skills with the ability to manage multiple priorities effectively.
• Excellent communication and collaboration skills with fluency in written and spoken English.

Why Novartis

Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

You’ll Receive

• Competitive salary
• annual bonus
• life insurance
• home office policy (home office 2x a week)
• retirement and wellbeing plans
• flexible working arrangements
• birthday day-off
• parental leave
• subsidized dining facilities
• health insurance
• employee recognition platform
• Gympass
• employee resource groups
• virtual self-development tools

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Skills Desired

Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives.