Job Opportunities

Apollomics is currently reviewing candidates for the following positions:

US Positions

Sr. Clinical Research Associate (CRA) / Clinical Trial Manager (CTM)

Based in Foster City, CA the Sr Clinical Research Associate (CRA) or CTM will be responsible for managing Vendors and Clinical Systems in support of a complex clinical trial/s and meeting clinical trial milestones in compliance with applicable clinical and regulatory standards with alignment of business needs. The Sr CRA/CTM will provide clinical study support for one or more clinical studies/programs, ensuring efficient delivery of clinical trials in a matrix environment. Will assist in managing…

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…

Research Scientist – Hangzhou China

This position works on discovering novel therapeutics for cancer!  The position is located in our Hangzhou China office. Primary Duties and Responsibilities: Work independently  in  a collaborative team  environment discovering novel therapeutics for cancer; Design, perform and optimize  assays for target identification,  validation,  mechanistic  study  as  well as biomarker study; Analyze and interpret  experimental  data,  communicate  with  team  members  and  collaborators  on working  progress; Summarize and present research results in the project and department meetings….

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…

Director of Regulatory Affairs – Hangzhou China

The Director of Regulatory Affairs will be responsible for all regulatory affairs in China.  This includes all government filings, reports, and responding to requests. This position is based in Hangzhou China. Primary Duties and Responsibilities: Set up the regulatory strategy development for responsible products; Coordinate with CFDA’s experts and medicine experts, and solve the problems of drug registration; Communicate with other related functions’ colleagues to explain Chinese regulation, requirement and RA plans; Track the applied…

Quality Assurance Specialist II – Hangzhou China

Primary Duties and Responsibilities: This position performs a variety of activities to ensure compliance with applicable manufacturing related regulatory requirements. Position may be filled at Manager level as well. The position is in Hangzhou, China. Primary Responsibilities: Performs a wide variety of activities to ensure compliance with applicable regulatory requirements Reviews manufacturing, environmental monitoring, and quality control data for products Ensures high-quality product comply with current Good Manufacturing Practices (GMP) and current Good Laboratory Practices…


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