Clinical Trial Coordinator

Há 3 dias

Brasil beBeeCareer Tempo inteiro R$80.000 - R$120.000
Job Opportunity

We are seeking a Clinical Trial Assistant to join our dynamic team. As a key member, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments.

About the Role
  • Assist in coordinating and administering clinical trials, ensuring compliance with protocols and regulatory requirements.
  • Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
  • Support the preparation of study-related materials, such as informed consent forms and case report forms.
  • Work collaboratively with cross-functional teams to facilitate communication and ensure smooth trial execution.
  • Contribute to tracking and reporting clinical trial metrics and milestones.
Required Qualifications
  • Bachelor's degree in a scientific or healthcare-related field.
  • Prior experience with ethics submissions.
  • 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.
  • Good level of English proficiency.
What We Offer
  • Variety of annual leave entitlements.
  • A range of health insurance options to suit your needs.
  • Competitive retirement planning offerings to maximise savings and plan for the future.
  • Global Employee Assistance Programme offering 24-hour access to a network of professionals for support.
  • Life assurance and flexible benefits tailored to your country.

We value diversity and inclusion, providing an accessible environment for all candidates. ICON is committed to equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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