About the role
As a Clinical Research Associate, you will play a crucial role in managing and monitoring clinical trials. Your responsibilities will include coordinating with investigators, ensuring data integrity, and adhering to regulatory standards. This contract role suits individuals with a foundational knowledge of clinical research and a passion for contributing to advancements in healthcare. You'll work in a collaborative environment, gaining valuable insights into the clinical research process while making a difference in patient care.
What you'll do
- Monitor clinical trial operations.
- Ensure compliance with regulatory requirements.
- Collect and analyze trial data.
- Collaborate with cross-functional teams.
What you'll need
- Bachelor's degree in life sciences.
- 1-3 years of experience in clinical research.
- Familiarity with clinical trial protocols.
Skills
Attention to detail
Organizational skills
Data analysis
Good to have
Knowledge of GCP guidelines
Project management skills
Benefits
- Competitive salary based on experience.
- Flexible working hours.
- Exposure to diverse clinical research projects.
Interested in this role?
It takes about two minutes. Free to apply — Hi5 Jobs never asks candidates for money.
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Questions about this job
What does a Clinical Research Associate do?
You will monitor clinical trials, ensure compliance, and coordinate with study teams.
What qualifications are necessary for this role?
A degree in life sciences and some experience in clinical research are preferred.
What is the work schedule for this position?
It is a hybrid role with both onsite and remote work options.
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