About the role
In this role, you will be responsible for monitoring clinical trials, ensuring they are conducted in accordance with regulatory requirements and the study protocol. You will serve as the primary point of contact between the clinical site and our client, facilitating communication to enhance trial execution. The position is ideal for individuals with a solid background in clinical research and a passion for advancing medical science.
You will manage site selection, training, and monitoring activities, as well as oversee data collection and ensure the integrity of trial results. This contract role allows for flexibility with a hybrid work model, supporting a balanced work-life approach while contributing to meaningful research efforts.
What you'll do
- Monitor clinical trials and ensure compliance
- Manage site selection and training
- Oversee data collection and integrity
- Serve as the primary contact for clinical sites
What you'll need
- Degree in life sciences or a related field
- Minimum of 3 years experience in clinical research
- Knowledge of clinical trial regulations
Skills
Good to have
Benefits
- Competitive contract salary
- Flexible work environment
- Opportunities for professional growth
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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