About the role
As a Clinical Research Associate, you will oversee clinical trials and ensure compliance with regulatory standards. Collaborating with clinical teams, you will monitor trial progress, conduct site visits, and maintain data integrity. This role is perfect for professionals with clinical research experience seeking a flexible contract position that contributes to significant healthcare outcomes.
Your expertise will play a vital role in the development of new therapies and treatments. Our client fosters a supportive environment for professional growth and offers the opportunity to work on innovative clinical projects. If you are detail-oriented and passionate about clinical research, we encourage you to apply.
What you'll do
- Monitor and report on clinical trial progress
- Conduct site visits and audits
- Ensure compliance with regulatory and ethical standards
- Collaborate with clinical teams to resolve issues
What you'll need
- Degree in life sciences or related field
- 3-7 years of experience in clinical research
- Familiarity with ICH-GCP guidelines
Skills
Good to have
Benefits
- Competitive salary and flexible work arrangements
- Exposure to diverse clinical projects
- Opportunities for professional training and development
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