Description
As a Clinical Trial Associate at ICON Strategic Solutions in São Paulo, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders. Key responsibilities include:
- Assisting in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
- Maintaining and organizing clinical trial documentation, including study files, essential documents, and regulatory submissions.
- Supporting the preparation of study-related materials, such as informed consent forms and case report forms.
- Working with cross-functional teams to facilitate communication and ensure smooth trial execution.
- Contributing to the tracking and reporting of clinical trial metrics and milestones.
You will bring relevant clinical research experience, along with the following qualifications and skills:
- Bachelor's degree in a scientific or healthcare-related field.
- Prior experience or strong interest in clinical research.
- Knowledge of clinical trial processes, regulations, and guidelines.
- Excellent organizational and communication skills.
- Ability to work collaboratively in a fast-paced environment with attention to detail.
- Willingness to travel as required (approximately 10%).
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:
- Competitive base salary and performance-related incentives.
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Learning and development opportunities through structured training and career pathways.