About the role
As a Clinical Research Associate, you will play a crucial role in managing clinical trials, from initiation to completion. Your responsibilities will include monitoring trial progress, ensuring compliance with Good Clinical Practice (GCP) guidelines, and collaborating with research teams to resolve any issues. This position is ideal for individuals who are detail-oriented and have a strong understanding of clinical research processes.
You will conduct site visits, prepare reports, and liaise with regulatory bodies to ensure that all aspects of the trials are conducted ethically and efficiently. Your expertise will be vital in maintaining the integrity of the data collected, ultimately contributing to advancements in medical science. If you are passionate about clinical research and want to make a difference, we encourage you to apply.
What you'll do
- Monitor clinical trials
- Ensure compliance with GCP
- Conduct site visits
- Prepare regulatory reports
What you'll need
- Bachelor's degree in life sciences
- 3-7 years in clinical research
- Knowledge of regulatory requirements
Skills
Good to have
Benefits
- Flexible working hours
- Professional development opportunities
- Health insurance
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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