Clinical Research Associate II

Location: Taipei, Taiwan; the role includes on-site monitoring visits at clinical trial sites.

Company

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

What you will do

• Monitor clinical investigative sites to ensure protocol-compliant execution of Phase 1–4 studies.
• Conduct site qualification, initiation, interim monitoring, and study closeout visits.
• Identify site issues, coordinate corrective actions, and influence site personnel to meet study objectives.
• Ensure data quality, timely data submission, safety-event reporting, and subject protection.
• Train site personnel on protocols and applicable regulatory requirements.
• Manage investigator payments, negotiate investigator and hospital agreements, and identify potential investigators and sites.

Requirements

• At least 3 years of site monitoring experience.
• Experience with on-site monitoring of investigational drug or device trials.
• Tertiary qualification in a health-related field such as medicine, science, or nursing is preferred.
• In-depth knowledge of clinical research regulations, ICH/GCP guidelines, and applicable local requirements.
• Strong planning, organizational, analytical, communication, and interpersonal skills.
• Ability to address clinical site issues, recommend corrective actions, and exercise sound judgment with integrity.

Culture & Benefits

• Work in a dynamic environment with competing projects and deadlines.
• Support hirify.global's focus on innovation, clinical quality, and improving patient outcomes.
• Equal opportunity employment environment.