About the role
As a Clinical Research Coordinator, you will oversee clinical trials from initiation to completion. Responsibilities include recruiting and screening participants, ensuring compliance with protocol, and maintaining study documentation. This role is suitable for individuals with a background in life sciences or research, and it offers the flexibility of hybrid work. You will collaborate with various stakeholders and contribute to advancing healthcare knowledge.
What you'll do
- Oversee clinical trial activities and participant recruitment
- Ensure adherence to study protocols and regulatory requirements
- Maintain accurate records and documentation
- Coordinate with investigators and regulatory bodies
What you'll need
- Bachelor's or Master's degree in a relevant field
- 1-3 years of experience in clinical research
- Knowledge of clinical trial regulations
Skills
Strong organizational and multitasking skills
Excellent communication abilities
Attention to detail
Good to have
Familiarity with clinical trial management software
Understanding of GCP guidelines
Benefits
- Flexible working hours
- Exposure to advanced research practices
- Networking opportunities in the clinical research field
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 working hours for this part-time role?
Working hours are flexible, allowing for a balance between research obligations and personal commitments.
What qualifications are needed?
A degree in life sciences or a related field is required, along with some experience in clinical research.
How many clinical trials will I manage?
You will manage multiple trials simultaneously, depending on the client’s requirements.
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