About the role
As a Clinical Trials Coordinator, your primary role will be to oversee the administrative aspects of clinical trials, including participant recruitment, data collection, and regulatory compliance. You'll work closely with investigators, study sponsors, and clinical staff to ensure that studies are conducted according to protocol and regulatory guidelines. This position suits individuals who are organized, detail-oriented, and possess strong analytical skills.
You will handle scheduling, documentation, and communicate with various stakeholders to ensure the smooth operation of trials. If you have a passion for advancing medical research and a desire to work in a dynamic environment, this role is perfect for you.
What you'll do
- Coordinate clinical trials and manage documentation
- Recruit and screen participants for studies
- Ensure compliance with regulatory requirements
- Maintain communication with study sponsors and investigators
What you'll need
- Bachelor's degree in life sciences or related field
- Experience in clinical research or trials
- Strong organizational and communication skills
Skills
Good to have
Benefits
- Flexible work hours
- Health benefits
- Professional development opportunities
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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