仲望咨询致力于为企业提供中高级专业人才的招聘解决方案。迄今已有23年多历史，现在已经成长为亚洲领先的专业猎头顾问公司之一。
Overview:
GluBio is a biotechnology company committed to developing innovative targeted protein degradation (TPD) drugs for the treatment of cancer, autoimmune, and other life-threatening diseases. GluBio is built by a group of seasoned drug developers with years of experience and expertise in TPD drug discovery. Our proprietary technology platform enables the rational design and discovery of novel TPD drugs to eliminate key disease targets. With rigor, diligence, courage, and dedication, we strive for success in our mission to conquer unmet medical needs. We are always eager to have highly motivated and enthusiastic talents join us to build future success together.
Position Summary:
We are seeking a high-performance-driven and self-motivated leader with a team player to lead the clinical pharmacology team to support all aspects of clinical pharmacology and pharmacometrics related activities in the full life cycle stages of advancing pipeline projects.
Key Responsibilities:
? Build, manage and lead the pharmacology team to support the clinical pharmacology activities of all clinical programs
? Collaborate with other functional leaders to deliver and supervise all pipeline programs' clinical pharmacology study development strategies and plans.
? Participate in designing clinical pharmacology studies, ensuring that clinical pharmacology study designs and documents meet global regulatory, compliance requirements and project timelines
? Design and perform early clinical studies (starting dose selection, dose-escalation plan, dose determination) in-house and/or in collaboration with external investigators/CROs
? Design and supervise internal scientists and external collaborators/CROs to guarantee the delivery of high-quality data and study reports enabling proper endorsement of stage-gate transition by BODs
? Work with clinical teams to develop and implement the clinical pharmacology development strategies and plans to enable the assessment of pharmacokinetics/ pharmacodynamics/efficacy/toxicity relationship of TPD drugs at all clinical stages
? Participate in interactions and meetings with health authorities (NMPA, FDA, EMA, etc.), responsible for the preparation and communication of required clinical pharmacology information
? Communicate research strategies and findings at internal meetings and external conferences
? Manage department budgets and internal/external resourcing