About the role
As a Clinical Research Associate, you will be responsible for managing and monitoring clinical trials, ensuring compliance with regulatory standards. Your role will involve site selection, initiation, monitoring, and closeout, making it ideal for professionals with a strong background in clinical research.
You will collaborate with medical professionals and research teams to ensure that trials are conducted effectively and ethically. This contract position allows for a hybrid work model, providing flexibility while contributing to vital research in the healthcare sector.
What you'll do
- Conduct site selection and initiate clinical trials.
- Monitor trial progress and ensure compliance.
- Prepare reports and documentation for regulatory bodies.
- Collaborate with study teams and healthcare professionals.
What you'll need
- Bachelor's degree in life sciences or related field.
- 2-5 years of experience in clinical research.
- Familiarity with clinical trial regulations.
Skills
Strong organizational and project management skills.
Excellent communication and interpersonal skills.
Ability to work independently and as part of a team.
Good to have
Certification in clinical research.
Benefits
- Competitive salary and benefits.
- Flexible working arrangements.
- Opportunity to work on impactful research.
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 core responsibilities of a Clinical Research Associate?
You will manage and monitor clinical trials, ensuring compliance with regulations.
What qualifications do I need for this position?
A degree in life sciences or related field with 2-5 years of clinical research experience is preferred.
Is this role hybrid?
Yes, the position offers a hybrid work model.
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