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Clinical Trials Specialist
2 weeks ago
On Q Recruitment is seeking a skilled Clinical Trials Specialist to lead the study start-up team and ensure the timely initiation of clinical trials.
The ideal candidate will have 1-2 years of experience in clinical research, preferably in regulatory submission or study start-up coordination. A strong understanding of GCP, ICH guidelines, and local regulatory requirements is essential.
The successful candidate will be responsible for:
- Leading and managing the study start-up team to ensure compliance with regulatory requirements and ICH-GCP guidelines.
- Developing and implementing SOPs and best practices to optimize the study start-up process.
- Providing expert guidance on HREC regulations and ensuring compliance with local practices.
In this role, you will have the opportunity to work with cross-functional teams and stakeholders to ensure the success of clinical trials.
