Job Title:
Senior Research Associate
About the Job:
This is an exciting opportunity to join our team as a Senior Research Associate. As a key member of our clinical research team, you will be responsible for conducting clinical research activities independently in accordance with ICH GCP and SOPs.
Responsibilities:
* Conduct clinical research activities independently in accordance with ICH GCP and SOPs.
* Identify and select investigators.
* Manage investigator meetings.
* Design and review study materials.
* Submit protocol documents for ethics approval.
* Perform site visits, including initiation, monitoring, and close-out visits.
* Maintain accurate study status reports.
* Ensure correct storage and accountability of study materials.
* Process case record forms.
* Deal with clinical queries.
Requirements:
* Master's or PhD in Life Science, Nursing, or Health Related field.
* At least 5 years' experience in on-site monitoring in global oncology studies.
* Strong knowledge of ICH-GCP.
* Professional use of English language.
Benefits:
* Varying annual leave entitlements.
* A range of health insurance options.
* Competitive retirement planning offerings.
* Global Employee Assistance Programme.
* Life assurance.
Others:
We are committed to providing an inclusive and accessible environment for all candidates. If you need any reasonable accommodations during the application process, please let us know. We welcome applications from individuals who may not meet all the requirements but believe they would excel in this role.