About the role
As a Clinical Research Coordinator, you will manage the logistics of clinical trials, including patient recruitment and data collection. The role requires attention to detail and strong organizational skills. You will work closely with investigators and regulatory bodies to ensure compliance with all study protocols. This hybrid position allows you to work both remotely and onsite, providing flexibility in your role.
What you'll do
- Coordinate and oversee clinical trials.
- Ensure compliance with study protocols and regulations.
- Recruit and manage study participants.
- Collect and analyze clinical data.
What you'll need
- Bachelor’s degree in Life Sciences or a related field.
- Experience in clinical research coordination.
- Familiarity with regulatory requirements.
Skills
Strong organizational skills.
Excellent communication skills.
Ability to work independently and as part of a team.
Good to have
Knowledge of clinical trial management software.
Benefits
- Competitive salary.
- Flexible hybrid working model.
- Opportunity to work on impactful research projects.
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 qualifications do I need for this role?
A degree in Life Sciences or related field is essential.
How long will this temporary position last?
The duration is estimated at six months, subject to project needs.
What are the working hours like?
Working hours may vary, but a standard commitment of 40 hours per week is expected.
How do I apply?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
What kind of studies will I be coordinating?
You will be involved in various clinical trials focusing on new therapeutic interventions.
Listing last updated