About the role
As a Clinical Trials Coordinator, you will oversee all aspects of clinical trials including planning, execution, and monitoring. Your role will involve coordinating with various stakeholders including investigators, sponsors, and regulatory bodies. This position is perfect for individuals who thrive in a fast-paced environment and have a passion for improving patient outcomes through research.
You will be working closely with clinical teams to ensure that trials are conducted according to protocol and regulatory requirements. This opportunity offers a dynamic work environment with a focus on collaboration and continuous learning.
What you'll do
- Coordinate clinical trial activities
- Ensure compliance with regulatory standards
- Manage documentation and reporting
- Communicate with stakeholders
What you'll need
- Degree in life sciences or related field
- 2+ years experience in clinical research
- Strong organizational skills
Skills
Strong communication skills
Attention to detail
Knowledge of clinical trial regulations
Good to have
Project management skills
Familiarity with data management systems
Benefits
- Health insurance
- Professional development opportunities
- Flexible working hours
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 key responsibilities of a Clinical Trials Coordinator?
You will coordinate clinical trial activities, manage documentation, and ensure compliance with regulatory standards.
What qualifications do I need for this role?
A degree in life sciences or a related field along with relevant clinical research experience is preferred.
Can fresh graduates apply?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
What is the work schedule like?
This is a full-time, onsite role with standard working hours.
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