About the role
In this role, you will monitor clinical trial sites, ensuring adherence to protocols and regulatory requirements. You will work closely with investigators and coordinating staff to guarantee data integrity and participant safety. This position is ideal for professionals who have a strong understanding of clinical processes and excellent communication skills. You will be an integral part of a dynamic team focused on advancing medical research.
What you'll do
- Monitor clinical trial sites for compliance and data integrity.
- Collaborate with investigators to ensure protocol adherence.
- Prepare and maintain study documentation and reports.
What you'll need
- Bachelor's degree in life sciences or a related field.
- Experience in clinical trial management.
- Strong knowledge of GCP and regulatory requirements.
Skills
Excellent communication skills.
Detail-oriented and organized.
Ability to work independently and in a team.
Good to have
Familiarity with statistical software.
Knowledge of pharmacovigilance.
Benefits
- Competitive salary with contract benefits.
- Opportunity to work on cutting-edge research.
- Professional development and training opportunities.
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 qualifications do I need for this position?
A degree in life sciences or related field is required, along with relevant clinical research experience.
Is this a full-time position?
This is a contract role with the potential for extension based on project needs.
What are the working hours?
Standard working hours are from 9 AM to 6 PM, Monday to Friday.
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