Job Opportunities

Apollomics is currently reviewing candidates for the following positions:

Director / Senior Director, CMC Management

Reporting to the Sr. Vice President of Process Development and Manufacturing, the Director / Senior Director, Chemistry Manufacturing and Controls will work closely with project teams and cross-functional teams in planning, budgeting, overseeing manufacturing activities in external CMOs, as well as integrating, tracking and communicating CMC activities for the Apollomics’ product development programs. Key responsibilities and knowledge and skills for the position are listed below. Lead the identification, selection and management of Contract Manufacturing Organizations (CMOs)…

Global Safety Director – Oncology

Reporting to the Chief Medical Officer, this position will provide strategic oversight of global 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…

Director, Clinical Pharmacology

Director, Clinical Pharmacology The Director of Clinical Pharmacology, 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…

Senior Director/Vice President, Regulatory Affairs

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…

Clinical Science Liaison

The Clinical Science Liaison (CSL) will serve as a value added resource to sites and investigators and to support the Company’s Clinical Development Programs. The CSL will be responsible for building and managing relationships with, Key Opinion Leaders (KOLs), clinical trial investigators and research staff to ensure full engagement throughout the course of the study. They will also work to build relationships, where appropriate, with patient groups, scientific organizations, and advocacy organizations. The primary focus…

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