Job Opportunities

Apollomics is currently reviewing candidates for the following positions:

US Positions

Vice President / Senior Medical Director Clinical Development

Reporting to the Chief Medical Officer (CMO), based in Foster City, the Vice President / Senior Medical Director of Clinical Development will have responsibilities associated with all aspects of design, setup, monitoring, and analysis of Phase 1-3 clinical trials. This person must have excellent analytical and communication skills, and the ability to interact effectively with other members of the team, as well as with study investigators and their staff, CROs and vendors operating on behalf…

China Positions

Head of China Safety – Hangzhou China

This position is responsible for all product safety in China.  The position is located in our Hangzhou China office. Primary Duties and Responsibilities: Closely monitor the  responsible products’ safety profile in Chinese  patients; Collaborate   with   teams   on  product   development   and  life cycle management  from a local safety perspective; Serve as China  Safety liaison to  internal/external customers; Work out  China risk management plan to specific products,  and lead the cross-functional team to implement,  manage the product…

Director / Vice President, Clinical Operations – Hangzhou China

This position may be filled at the Director, Senior Director, or Vice President level.  The position is located in Hangzhou     China.  This position’s responsibilities will include oversight for clinical study conduct including leading internal and external (CRO) sub-teams, study planning, budgeting, and financial oversight, vendor/partner management, monitoring study, and program timelines. Primary Duties and Responsibilities: Anticipate project requirements and institute appropriate actions to ensure timelines and project goals are met. Oversight of designated activities outsourced…

Clinical Trial Manager – Hangzhou China

This position serves as a Clinical Research Associate / Clinical Trial Manager in our Hangzhou China office. Primary Duties and Responsibilities: Prepare and organize meetings; EC communication, submit and track EC approval; Facilitate the contracting  process  by negotiating  and signing  contracts  with  the relevant  institutions, investigators and other clinical study personnel; Provide study progress  report,  perform routine monitoring visits and provide monitoring visit reports; Ensure all data records and reports are completed correctly and consistent…


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