About the role
As a Clinical Research Associate, you will be responsible for coordinating and monitoring clinical trials, ensuring compliance with regulatory requirements and study protocols. You will collaborate with various stakeholders including investigators, participants, and regulatory bodies to ensure the successful execution of clinical studies. This role is ideal for professionals passionate about advancing medical research and improving patient outcomes. The team offers a supportive environment with opportunities for professional development and growth in the clinical research field.
Your daily tasks will include site selection, initiation, monitoring visits, and closeout activities, along with conducting regular visits to clinical trial sites. You will also be responsible for data collection, documentation, and ensuring adherence to Good Clinical Practice (GCP) guidelines.
What you'll do
- Coordinate and monitor clinical trials to ensure compliance
- Conduct site selection and initiation visits
- Ensure proper documentation and data integrity
- Communicate with stakeholders regarding study progress
- Provide training and support to site staff
What you'll need
- Bachelor's degree in life sciences or related field
- 2-5 years of experience in clinical research
- Knowledge of GCP and regulatory requirements
Skills
Good to have
Benefits
- Competitive salary based on experience
- Opportunities for professional development
- Supportive team environment
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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