About the role
In this Clinical Research Associate position, you will coordinate and monitor clinical trials, ensuring compliance with protocols and regulations. You will be responsible for data collection, site visits, and reporting findings to the project manager. This role is ideal for experienced professionals looking for flexible work arrangements.
The hiring company fosters an innovative environment, encouraging team members to contribute ideas and solutions. You will gain exposure to various aspects of clinical research, enhancing your skills and career prospects in the healthcare industry.
What you'll do
- Coordinate clinical trials and monitor compliance
- Collect and analyze trial data
- Conduct site visits and prepare reports
- Collaborate with cross-functional teams
What you'll need
- Bachelor's degree in Life Sciences or related field
- 2-4 years of experience in clinical research
- Strong organizational and communication skills
Skills
Attention to detail
Analytical skills
Project management skills
Good to have
Familiarity with clinical trial regulations
Experience with data management software
Benefits
- Flexible working hours
- Competitive salary
- Opportunities for professional development
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 duties of a Clinical Research Associate?
You will monitor clinical trials and ensure compliance with protocols.
What type of experience is required?
2-4 years of experience in clinical research is preferred.
Is this a remote position?
This is a hybrid role, combining onsite and remote work.
What qualifications do I need?
A degree in life sciences or related field is required.
How can I apply for this position?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
Listing last updated