Clinical Trial Associate (APAC)

Benefits

Parental leave

Not verified

Non-birth-parent leave

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Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

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Relocation assistance

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Childcare support

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Learning budget

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Verification

Not verified checked Jun 13, 2026

Salary

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401(k) match

Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)

$81,444 U.S. median for this role

Projected growth (BLS Employment Projections)

+6.9% - Faster than average

Matched to SOC 29-1141 - Healthcare aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Schedule

Shift type

Not verified

Weekend work

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Application

Cover letter

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Assessment

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Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Clinical Trial Associate (APAC) Asia-Pacific (APAC), Singapore Position Overview The Clinical Trial Associate (CTA) at Bicara Therapeutics plays a critical role on the Clinical Operations team by supporting the planning, execution, and management of clinical trials. The CTA will work closely with Clinical Trial Managers (CTMs) and other cross-functional teams to ensure that trials are conducted efficiently, in compliance with regulatory requirements, and in accordance with the study protocol. This position will report to the APAC Clinical Trial Manager, Clinical Operations. This position is remote, with a strong preference for candidates located within the APAC region. Responsibilities - Assist in the coordination and management of clinical trials, including study start-up, maintenance, and close-out activities in close collaboration with Clinical Trial Managers and CRO. - Support Clinical Trial Managers in overseeing CRO deliverables, timelines, issue escalation, and overall study operational performance across assigned regions and sites. - Proactively identify and escalate operational risks, delays, or quality issues to the Clinical Trial Manager. - Maintain, organize, and update essential study documentation to ensure they are complete, accurate, and audit-ready at all times. - Facilitate effective communication among study sites, Clinical Trial Managers, and other stakeholders by managing correspondence, coordinating meetings, and distributing study-related information, including preparing agendas, tracking action items, documenting decisions, and following up on outstanding deliverables. - Support the site start-up and activation process, including collection and tracking of essential documents in accordance with the EDP; coordination of EC/RA submissions and approvals; vendor coordination; and follow-up with CRO teams to

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