Clinical Trial Manager
2 weeks ago
The successful candidate will contribute to the efficient management of clinical trials, ensuring that projects are conducted in accordance with applicable SOPs, regulations and ICH guidelines.
Key Responsibilities:- Perform site qualification visits, discussing protocol and study requirements with investigators and other trial staff.
- Support feasibility, site selection and start-up activities, including leading the preparation of HREC submissions with sites.
- Negotiate site budgets and assist with the execution of site contracts with support from project managers.
- Perform site initiation visits, training investigators and other trial staff in the protocol and data collection methods.
- Perform interim monitoring visits, ensuring adherence to protocol and monitor participant source data via source document verification.
- Oversee all aspects of study site management to ensure high-quality data.
The ideal candidate will possess a strong understanding of ICH-GCP principles and have at least 3-4 years of experience in monitoring clinical trials. Additionally, they should hold an undergraduate degree in life sciences or a related field.
As a member of our team, you can expect a challenging yet rewarding role that offers opportunities for growth and development. We prioritize teamwork, communication, and collaboration to deliver high-quality results.
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