Job Opportunities

Apollomics is currently reviewing candidates for the following positions:

US Positions

Senior Director/Vice President, Regulatory Affairs – Foster City, CA USA

Reporting to the Chief Medical Officer, the Senior Director/Vice President, Regulatory Affairs will serve as the global  regulatory  leader  for  defining  and  implementing  the  regulatory  strategy  across Apollomics  product  pipeline.  He/she is responsible for the regulatory filing strategy for US FDA and all global interactions and filings, annual reports, as well as responses to requests from these agencies. In effect, this individual will provide regulatory leadership to cross functional teams ensuring effective communication with business…

Senior Medical Writer – Foster City, CA USA

Senior Medical Writer This is a senior medical writing position that requires scientific knowledge along with clear writing and communication skills. The position is in Foster City, however, open to remote candidates. The primary focus is on scientific medical writing, which includes researching, writing and editing protocols, investigator brochures, DSUR annual reports, preparation of abstract and scientific presentations, and supervising external vendor(s) in writing clinical study reports. This includes the ability to summarize data from…

Clinical Pharmacology (Contractor) – Foster City, CA USA

The Clinical Pharmacology Contractor, reporting to the Chief Medical Officer, will represent Clinical Pharmacology on development project teams. The qualified candidate will contribute to the development of clinical study concepts and protocols, execution of clinical pharmacology studies, population PK/PD analyses, clinical study reports, and relevant components of regulatory submission documents. He/she will review non-clinical as well as clinical pharmacology development plans and assist in the interpretation of preclinical data and extrapolation of implications for human…

Contracts Specialist Paralegal – Foster City, CA USA

This paralegal will draft, review and negotiate a wide array of contracts for the company’s global clinical development operations and will provide them with related advice and counsel. The paralegal will also provide contract support in the areas of Discovery, CMC, and Translational Medicine. The ideal candidate will have experience with clinical trial contracting with a high degree of judgement, flexibility, and organizational skills. Position is full-time regular employee status;  open to filling role on…

China Positions

Head of China Quality – Hangzhou China

This position heads all Quality policies, procedures, and compliance matters in China.  The position is located in our Hangzhou China office. Primary Duties and Responsibilities: Design, implement and optimize operational and quality policies and procedures, ensuring compliance with  all applicable  regulations  (e.g.  GLP,  GCLP,  CUA, etc.), guidance,  and standards while ensuring business  processes are designed to maximize value for internal and external clients; Collect and monitor performance metrics,  including identification of trends that require  preventive…

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…

Administrative Assistant – Hangzhou China

This Administrative Assistant position is located in our Hangzhou China office. Primary Duties and Responsibilities: Answer, screen and transfer inbound  phone calls; Receive and direct visitors and clients; General clerical duties including photocopying, fax, and mailing; Schedule and coordinate meetings, appointments and travel arrangements for managers or supervisors; Prepare agendas for meetings and prepare schedules; Record, compile, transcribe and distribute minutes of meetings;  Maintain office supply inventories; Resolve other administrative problems and inquiries. Qualifications: College…

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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