Senior Clinical Research Associate

Location: Shanghai, China

Company

Develops innovative medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

• Serve as a primary sponsor point of contact for investigative sites and strengthen site partnerships.
• Align, train, and motivate site staff and principal investigators on clinical trial goals, protocols, and patient treatment principles.
• Conduct site evaluation, training, routine on-site and off-site monitoring, and site close-out activities.
• Develop site engagement, patient recruitment, and retention strategies based on the disease journey and therapeutic area.
• Perform continuous risk assessment, resolve site risk signals, and implement corrective and preventive actions.
• Ensure data quality, safety reporting, regulatory inspection readiness, and investigator payment compliance.

Requirements

• Bachelor's degree or appropriate tertiary qualification in a health-related discipline such as medicine, science, pharmacy, or nursing.
• At least 3 years of clinically related experience, including preferably 2 years of independent monitoring of investigational drug or device trials.
• Knowledge of risk-based monitoring, clinical trial execution, therapeutic areas, local regulatory requirements, ICH/GCP guidelines, and applicable policies.
• Advanced communication, presentation, planning, organizational, interpersonal, and cross-functional collaboration skills.
• Ability to independently assess clinical site issues, apply critical thinking, and use technology and monitoring tools effectively.
• Ability to mentor and train less experienced clinical research associates.

Culture & Benefits

• Work in a fast-paced environment with competing projects and deadlines.
• Participate in global or local task forces and initiatives.
• Operate according to integrity, leadership, quality, and compliance standards.
• Equal opportunity employment with a focus on innovation and community impact.