About this role
The CTA supports the planning, execution, and management of clinical trials by coordinating with CROs and cross-functional teams. Key duties include maintaining essential study documentation, managing site start-up activities, and ensuring regulatory compliance.
Requires a Bachelor's degree in life sciences or nursing and at least 3 years of clinical research experience, including 1 year in the biopharmaceutical industry. Proficiency in ICH-GCP and experience with oncology trials or global study support is preferred.
What they're looking for
Clinical Trial ManagementICH-GCPRegulatory ComplianceTMF ManagementCRO OversightSite Start-upOncology ResearchData Management
Frequently asked questions
What does a Clinical Trial Associate (APAC) at Bicara Therapeutics do?
The CTA supports the planning, execution, and management of clinical trials by coordinating with CROs and cross-functional teams. Key duties include maintaining essential study documentation, managing site start-up activities, and ensuring regulatory compliance. Requires a Bachelor's degree in life …
What skills does this Clinical Trial Associate (APAC) role need?
Key skills for this role include Clinical Trial Management, ICH-GCP, Regulatory Compliance, TMF Management, CRO Oversight, Site Start-up.
How much does a Clinical Trial Associate (APAC) at Bicara Therapeutics pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Clinical Trial Associate (APAC) role remote, hybrid, or on-site?
This role is remote ok, based in Singapore.
How do I apply for this Clinical Trial Associate (APAC) role?
You can apply directly on Bicara Therapeutics's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.