About the role
In this part-time position, you will oversee the planning, implementation, and monitoring of clinical trials. You will collaborate with medical professionals, patients, and regulatory bodies to ensure compliance with protocols and safety standards. This role is ideal for someone who has experience in clinical research and is looking to balance work with other commitments.
You will play a key role in coordinating research activities, maintaining study documentation, and ensuring accurate data collection. Join our team to contribute to groundbreaking research that enhances patient care and advances medical knowledge.
What you'll do
- Coordinate and manage clinical trial activities
- Ensure compliance with regulatory requirements
- Collaborate with medical teams and participants
- Maintain accurate records and documentation
What you'll need
- Bachelor's degree in life sciences or related field
- 3-6 years of experience in clinical research coordination
- Familiarity with Good Clinical Practice (GCP) guidelines
Skills
Strong organizational and management skills
Excellent communication abilities
Attention to detail and accuracy
Good to have
Experience with clinical trial management software
Certification in clinical research
Benefits
- Flexible working hours
- Competitive salary
- Opportunity to work on innovative research projects
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 are needed for this role?
A degree in life sciences or a related field, along with prior experience in clinical research.
Is this a full-time position?
No, this is a part-time hybrid role with flexible hours.
What experience is preferred?
3-6 years of clinical research experience is required.
How can I apply?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
Listing last updated