About the role
As a Clinical Research Coordinator, you will oversee clinical trial operations, ensuring compliance with protocols and regulations. Your role involves coordinating with various stakeholders, including investigators, sponsors, and regulatory bodies. You will be responsible for data collection, management, and ensuring the integrity of the trial process. This position suits individuals with strong organizational skills and attention to detail. Join a passionate team dedicated to advancing healthcare through clinical research.
What you'll do
- Coordinate clinical trial activities
- Ensure compliance with regulatory requirements
- Manage data collection and documentation
What you'll need
- Bachelor's degree in life sciences or a related field
- 3+ years of experience in clinical research
- Knowledge of clinical trial regulations
Skills
Strong organizational skills
Excellent communication skills
Attention to detail
Good to have
Experience with electronic data capture systems
Knowledge of Good Clinical Practice (GCP)
Benefits
- Flexible working hours
- Networking opportunities within the industry
- Possibility of contract renewal
Interested in this role?
It takes about two minutes. Free to apply — Hi5 Jobs never asks candidates for money.
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Questions about this job
What are the main duties of a Clinical Research Coordinator?
You will manage clinical trials, coordinate with participants, and ensure compliance with protocols.
Is this position full-time or part-time?
This is a contract position with a hybrid work mode.
What qualifications do I need?
A degree in life sciences and experience in clinical research are required.
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