Clinical Research Associate II (Clinical Research)

Location: Chengdu, Sichuan, China; North Chicago, Illinois, United States

Company

hirify.global develops innovative medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

• Serve as the primary point of contact for investigative sites and build effective partnerships with investigators and site staff.
• Train and support principal investigators and site teams on clinical trial goals, protocols, treatment principles, and applicable requirements.
• Conduct site evaluation, initiation, routine, and closeout monitoring in accordance with protocols, monitoring plans, GCP, ICH guidelines, regulations, and hirify.global SOPs.
• Assess site risks, coordinate preventive and corrective actions, and collaborate with central monitoring teams to address safety and study-performance signals.
• Support patient recruitment and retention, data quality, safety-event reporting, audit readiness, and investigator payment processes.
• Identify potential investigators and sites, contribute to clinical initiatives, and mentor less experienced CRAs.

Requirements

• Bachelor’s degree or appropriate tertiary qualification in a health-related discipline such as medicine, science, or nursing.
• At least 1 year of clinically related experience, including at least 6 months of clinical research monitoring for investigational drug or device trials.
• Experience with risk-based monitoring and onsite and offsite monitoring activities.
• Knowledge of therapeutic areas, clinical trial science, local regulatory and legal requirements, ICH/GCP guidelines, and applicable policies.
• Strong planning, organization, communication, presentation, collaboration, interpersonal, and critical-thinking skills.
• Ability to manage competing deadlines, resolve site issues, use clinical technology and tools, and deliver high-quality outcomes with integrity.

Culture & Benefits

• Work focused on developing medicines and solutions for serious health conditions.
• Collaboration with investigators, site staff, internal stakeholders, and central monitoring teams.
• Opportunities to participate in global and local task forces and initiatives.
• Equal opportunity employment and a strong focus on integrity, innovation, and community impact.