Clinical Research Coordinator
1 day ago
Cyden Ltd is seeking a highly skilled Study Monitor to oversee the progress of clinical and application research/trials. The successful candidate will ensure all research is conducted, recorded, and reported in accordance with Protocols, SOPs, ICH-GCP and applicable regulatory requirements.
Key Responsibilities
- Provide a global evaluation of all investigations commissioned and executed.
- Ensure collection of the required essential documents for study start-up and throughout the conduct of a trial.
- Conduct on-site training and motivate the investigators.
- Verify patient data and ensure adherence to protocol, GCP and internal SOPs.
- Maintain all files pertaining to the clinical trials, track study progress and ensure timely quality updates are provided.
- Perform routine site visits and assessments.
Requirements
- Strong interest in clinical trial and application research.
- Experience of working in a similar role.
- Excellent organisational, planning, and interpersonal skills.
- Ability to work under pressure and demonstrate initiative and problem-solving skills.
- Knowledge of clinical trials regulations, ICH-GCP and excellent literacy, numeracy, and IT skills.
What We Offer
Cyden Ltd is a dynamic and innovative company that offers a challenging and rewarding work environment. The successful candidate will have the opportunity to work with a talented team of professionals and contribute to the success of our clinical and application research team.
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