About the role
As a Research Associate in Clinical Trials, you will be responsible for coordinating and overseeing various clinical studies. Daily tasks will include recruiting participants, managing data collection, and ensuring compliance with regulatory standards. This position suits candidates with a keen interest in clinical research and a desire to contribute to new medical advancements. You will work closely with a team of professionals dedicated to improving patient outcomes through innovative research initiatives.
What you'll do
- Coordinate clinical trial protocols and procedures.
- Recruit and manage study participants.
- Ensure compliance with regulatory requirements.
What you'll need
- Bachelor's degree in Life Sciences or related field.
- Experience in clinical trial management.
- Strong organizational and communication skills.
Skills
Knowledge of clinical research methodologies.
Proficient in data management and analysis.
Excellent interpersonal skills.
Good to have
Familiarity with regulatory guidelines.
Experience with patient recruitment strategies.
Benefits
- Opportunity to work on cutting-edge research.
- Professional development and training.
- Competitive salary and benefits package.
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
Questions about this job
What qualifications are required for this role?
A degree in Life Sciences or a related field, along with experience in clinical research, is preferred.
How long is the contract for this position?
The initial contract is for 12 months, with potential for extension based on project needs.
What is the work schedule like?
The work schedule is typically Monday to Friday, 9 AM to 5 PM.
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