
Senior Clinical Site Manager
1 week ago
We are seeking a highly skilled professional to lead our clinical research initiatives as a Senior Clinical Research Associate.
- This role involves developing and maintaining strong relationships with clinical sites, ensuring seamless site interactions throughout the trial lifecycle.
- The ideal candidate will be responsible for conducting clinical study site management/monitoring activities in compliance with international regulatory standards, sponsor guidelines, local laws and regulations, protocol requirements, and associated documents.
To succeed in this position, candidates should possess a Bachelor's degree with 3 years of experience in a similar role or an equivalent combination of education, training, and experience. Ophthalmic experience is highly preferred.
Main Responsibilities:
- Developing in-depth knowledge of study protocols and contributing to site selection and validation activities.
- Participating in audit/inspection activities as needed.
- Managing and maintaining accurate information and documentation within various systems, adhering to timelines and guidelines.
About Us:
We value the daily practice of prioritizing kindness, operational excellence, cultivating joy, and scientific rigor in our work.
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