About the role
As a Research Associate in Clinical Trials, you will assist in the planning and execution of clinical research studies. You'll collaborate with investigators and study coordinators to ensure that all regulations are met and that trials are conducted according to protocol. This role is perfect for recent graduates or those with some experience in clinical research.
Responsibilities include data collection, participant recruitment, and maintaining study documentation. You'll also engage in monitoring and reporting of trial progress to ensure compliance with ethical standards. If you are detail-oriented and passionate about advancing medical research, this position could be a great fit for you.
What you'll do
- Assist in the planning and execution of clinical trials.
- Collect and analyze data from study participants.
- Maintain accurate and timely trial documentation.
- Monitor compliance with regulatory and ethical standards.
What you'll need
- Bachelor's degree in life sciences or related field.
- 1-3 years of experience in clinical research preferred.
- Knowledge of clinical trial regulations.
Skills
Good to have
Benefits
- Exposure to innovative clinical research.
- Flexible working hours.
- Networking opportunities with industry professionals.
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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