Job Title:

Pre-clinical & Clinical Project Manager

Location: Taipei

Job Responsibilities

• Manage projects timeline and budget from research, toxicology studies, IND filing to early-stage clinical
• Develop and maintain detailed target product profiles (TPPs), project plans and risk & mitigation plans
• Coordinate with cross-functional teams to drive project timeline, organize/ lead project meetings, and track action items until resolution
• Evaluate, negotiate, execute, and coordinate all outsourced activities including but not limited to vendors, CROs, and CDMOs
• Collaborate with consultants for clinical and regulatory activities, including communication with regulatory agencies, clinical sites etc.

Job Requirements

• Master’s Degree in life sciences, nursing, pharmacy or equivalent (Ph.D. Degree is highly preferred)
• More than six years of related preclinical and/or clinical experience of biologics in the biotechnology/pharmaceutical industry
• In-depth knowledge of pharmaceutical development and clinical development
• Experience in project management and clinical/regulatory affairs
• Proficient in the Microsoft suite of business software including MS Projects and Access and other clinical/regulatory softwares
• Evidence of building relationships with and managing expectations of stakeholders at all levels and externally, to persuade on business benefits and gain acceptance to changes
• Excellent written and oral communication, collaboration and “think-out-of-the box” problem-solving skills; performance-driven, reliable team player with strong sense of responsibility
• Comfortable meeting deadline in a fast-paced biotech environment

Contact

Email: career@hanchorbio.com

please visit: https://www.hanchorbio.com/en/recruitment