Job Opportunities

Apollomics is currently reviewing candidates for the following positions:

US Positions

Senior Clinical Trial Manager / Clinical Program Manager, Clinical Operations

Based in Foster City, reporting to the Sr. Director, Clinical Operations, the Senior Clinical Trial Manager (SrCTM) or Clinical Program Manager (CPM) will be responsible for managing and meeting clinical trial milestones in compliance with applicable clinical and regulatory standards with alignment of business needs. The Sr. CTM/CPM is accountable for clinical trial management, including Clinical Research Organization (CRO), vendor, and/or cross-functional team meeting management and representation as a study lead.  This position works in…

Safety Director / Senior Safety Director

Reporting to the Chief Medical Officer, this position will provide strategic oversight of pharmacovigilance (PV) operational activities in support of monitoring the safety profiles of all Apollomics products via best practices in PV to ensure global compliance with FDA and international regulatory reporting requirements in alignment with global health authority guidance including GCP/ICH, compliance requirements, and Apollomics corporate and business partners policies. Primary Duties and Responsibilities Accountable for day to day operational performance and compliance…

CMC Operations Manager

The CMC Operations Manager will have an emphasis on chemistry and be a key player on our CMC team (small molecules). The CMC Operations Manager will support our global pre-clinical and clinical development and commercial programs.  Reporting directly to the Sr. Director, CMC (small molecules), this role will oversee and support strategy, plans and objectives for all chemistry, manufacturing, and controls (CMC) activities. Responsibilities: Plan and suppor stage-appropriate development for drug substance, drug product and…

Associate Manager / Manager Regulatory Affairs

The Opportunity: The Associate Manager/ Manager Regulatory Affairs will be responsible for assisting in the strategic and administrative regulatory aspects of oncology drug product development (pre-submission through post-approval).  This position reports to the Senior Director of Regulatory Affairs. Professional Responsibilities: Individual contributor supporting the regulatory deliverables, as part of the larger organizational goals. Under direction, represents department on assigned projects (e.g. study teams). Assist RA management in providing guidance and addressing issues, may work with…

Vice President / Senior Medical Director Clinical Development – Foster City, CA USA

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

Director / Sr. Director, CMC management – Small Molecules

This position requires strong experience in small molecule chemistry both drug substance and drug product. This position is in Hangzhou China and reports to the Senior Director CMC who is located in Foster City, California. Description of key responsibilities: Responsible for all CMC-related activities for Drug substance and Drug product small molecule drugs – Taking the molecule from early discovery to proof of concept, pilot scale, process scale up to commercial production,  Responsible for technology…

Sr. Director/ VP, Oncology PreClinical Development Science

Description: Reporting to the General Manager/Head of Science, China, this position will have a leadership role in leading the preclinical development team in oncology and translational science to support pipeline development from discovery to IND. The successful candidate will lead, design and conduct biological experiments to investigate potential oncology targets and pathways in concert with new target selection and validation, in vitro assay development, in vivo pharmacology and toxicology studies and other IND enabling studies…

Senior Director / VP Business Development – Hanzhou or Shanghai, China

Description: Reporting to the General Manager, China, this position will have a leadership role in developing and expanding the growth and value creation opportunities including partnerships, alliances, deals, and in-licensing and acquisition of novel therapeutics. The candidate will work closely with the internal cross functional team members and the executive management team to advance initiatives by sourcing, evaluating, structuring, and negotiation deals to support the corporate vision and goals of Apollomics. This individual will drive…

Director / Senior Director, Data Management – Hangzhou, China

Description: Reporting to the Director / V.P. Clinical Operations in   Hangzhou China, this position is responsible for the performance of the company clinical data management (CDM) function.  The Director/Sr. Director recommends and executes strategies in collaboration with Senior Management, Apollomics US to ensure successful outcomes for projects/studies. This position has advanced knowledge of Electronic Data Capture and industry standards, and advanced skills partnering with contract research organizations (CROs) and other third-party vendors.  This position requires…

Director / Senior Director, Statistics/Data Science; Head of Biometrics – Hangzhou, China

Description: Reporting to the Chief Medical Officer and dotted line to the General Manager / Head of Science in China, this position is responsible to provide statistical oversight and lead the clinical development of assets in study design, data analysis, interpretation of results independently with minimal supervision, authors regulatory responses and other documents with minimal supervision. This position interacts with global project teams and the NMPA, as well as contract research organization (CRO) programmers and statisticians….

Director / Senior Director, Pharmacology – Hangzhou, China

Description: Reporting to the Director / V.P. Clinical Operations in Hangzhou China, this position is responsible for the design, execution and leadership and implementation of Clinical Pharmacology strategy across the Apollomics’ China portfolio of agents and programs.  He/she will represent Clinical Pharmacology on development project teams and 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….

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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