About the role
As a Clinical Trials Coordinator, you will oversee the day-to-day operations of clinical trials, including participant recruitment and data collection. You will work closely with clinical staff to ensure that all trial protocols are followed and that regulatory requirements are met. This role is ideal for individuals with a strong background in clinical research and excellent organizational skills. The supportive team offers opportunities for professional development and growth within the field of clinical trials.
What you'll do
- Oversee daily operations of clinical trials
- Coordinate participant recruitment and scheduling
- Ensure compliance with regulatory requirements
- Maintain accurate trial documentation
What you'll need
- Bachelor's degree in life sciences or related field
- 2-5 years of experience in clinical trials
- Strong knowledge of regulatory guidelines
Skills
Excellent organizational skills
Strong communication abilities
Ability to work under pressure
Good to have
Familiarity with clinical trial management software
Knowledge of data analysis methods
Benefits
- Competitive salary package
- Opportunity for professional development
- Collaborative work environment
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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Questions about this job
What are the main responsibilities in this role?
You will manage trial operations, coordinate with clinical staff, and ensure compliance with protocols.
Is this a full-time position?
This is a contract position with the possibility of extension based on project requirements.
What qualifications do I need?
A degree in life sciences or a related field and experience in clinical trials is preferred.
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