Associate, Study Management III/CTM III (Clinical Research)

Location: Global role; may be located virtually. The posting references Shanghai, China.

Company

hirify.global discovers and delivers medicines and solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

• Lead study-level oversight and contribute to the planning, execution, and closure of one or more global Phase 0–4 clinical trials.
• Support cross-functional study leadership, stakeholder engagement, meeting facilitation, documentation, and delivery against timelines and budgets.
• Manage external vendors, including RFPs, selection, scopes of work, deliverables, and risk management.
• Develop and execute global recruitment strategies, feasibility activities, mitigation plans, and retention initiatives.
• Manage study materials, CTMS, eTMF, EDC, IRT, ePRO, investigational products, and study supplies while supporting inspection readiness.
• Provide stakeholder training, support global submission strategies, and contribute to process improvement and subject-matter expertise.

Requirements

• Bachelor’s degree or equivalent required.
• At least 4 years of progressive pharmaceutical or clinical research experience.
• Competence in SOPs, ICH/GCP, global regulations, and quality procedures.
• Experience with EDC, IRT, CTMS, and eTMF systems.
• Strong analytical, critical-thinking, organizational, time-management, interpersonal, and communication skills.
• Proficiency in business and technical English, both oral and written, is required.

Nice to have

• Exposure to study activities from initiation through completion.
• Experience with global studies.

Culture & Benefits

• Work in a global, cross-functional clinical study environment.
• Operate independently while receiving support from Study Project and Associate Managers.
• Contribute to innovative medicines and solutions addressing serious health challenges.
• Equal opportunity employment and a commitment to integrity, innovation, and community service.