About the role
As a Clinical Research Associate, you will oversee clinical trials from initiation to completion, ensuring adherence to study protocols and regulatory requirements. Your responsibilities will include site selection, initiation, monitoring, and close-out, maintaining data integrity and compliance throughout the trial process.
This contract position is ideal for detail-oriented professionals who excel in a dynamic research environment. If you are passionate about advancing healthcare through clinical research, this role offers the flexibility of remote work, allowing you to manage your schedule while contributing to vital studies.
You will collaborate with various stakeholders to enhance patient safety and data quality, playing a crucial part in the success of clinical trials.
What you'll do
- Monitor clinical trials and ensure compliance with protocols.
- Conduct site visits and provide training for site staff.
- Collaborate with project teams to resolve issues.
- Prepare and review study documentation.
What you'll need
- Degree in life sciences, nursing, or a related field.
- 2-4 years of experience in clinical research.
- Strong understanding of GCP and regulatory guidelines.
Skills
Good to have
Benefits
- Flexible remote work environment.
- Opportunity to work on diverse clinical trials.
- Professional growth and learning opportunities.
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