(Associate)Project Manager, Clinical Biomarkers

General Description:

Manage biomarker related operational part for collaborative/superhigh way clinical trials

Essential Functions of the job:

• Independently provide biomarker related expertise for clinical trials conduction from an operational perspective.
• Mainly focus on collaborative/superhigh way studies and build good relationships with collaborators.
• Be responsible for biomarker operation work including lab vendor selection, lab key document review, lab performance oversight and management, etc.
• Collaborate and communicate with internal and external stakeholders, to drive biomarker related budget, timeline, quality management to make sure biomarker strategy is implemented.
• Lead CDx studies and communicate with both device partners and lab vendors to make sure CDx strategy is implemented when needed, especially for CDx China solution.
• Participate in clinical study team meetings, providing updates and insights related to biomarker activities and progress.
• Collaborate with data management team on EDC setting, biomarker data review, and work with lab vendor to resolve the data related issues when needed.
• Other assigned work as needed.

Qualifications:

• Master or above in biology/medical major.
• Experience in the pharmaceutical industry and/or academia is preferred
• Understanding of scientific concepts and experience in translational research and oncology biomarker development.
• At least 3 years project management experience
• Proven organizational and project management skills and the ability to manage cross-functional efforts.
• Ability to work effectively on multiple oncology programs in a fast-paced, dynamic environment
• Excellent verbal and written English communication skills

Travel: Occasionally

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