Senior Clinical Trials Strategy & Operations

CANSINO BIOLOGICS (HONG KONG) LIMITED; Hong Kong; On-site; HKD 600,000 - 900,000; Full time

Job summary

CANSINO BIOLOGICS (HONG KONG) LIMITED is seeking a clinical research professional to lead development strategies for biological products. You will finalize study designs with rigorous statistics, align resources with key opinion leaders, and draft clinical study reports for regulatory reviews.

The role requires robust project planning and cross-functional collaboration, with emphasis on quality, compliance, and effective communication with investigators and regulatory bodies.

Qualifications

• Master's degree or above in Preventive Medicine, Public Health, Clinical Medicine, Statistics, Life Sciences, Biopharmaceuticals, or related subjects.
• Three years of relevant work experience in clinical research, drug development, clinical trial management, or related fields is preferred.
• Strong capabilities in project planning, management, operations, and coordination with a strong sense of responsibility.
• Excellent communication and teamwork skills with the ability to collaborate across departments.
• Rigorous work attitude with attention to detail and strict compliance in execution processes.
• Forward-thinking mindset with the ability to contribute to protocol development and optimization.

Responsibilities

• Conduct research to create clinical development strategy and plans for biological products and finalize study designs.
• Assess study feasibility across target countries and clinical centers and establish feasible trial designs.
• Prepare and review clinical trial documents for ethics committees and regulators to secure approvals.
• Develop standardized trial operations, protocols and trainings, and manage trial resources and supply.

Skills

Project planning

Management

Operations

Coordination

Education

Master's degree or above in related life sciences

Job description

CANSINO BIOLOGICS (HONG KONG) LIMITED is seeking a clinical research professional to lead development strategies for biological products. You will finalize study designs with rigorous statistics, align resources with key opinion leaders, and draft clinical study reports for regulatory reviews.

The role requires robust project planning and cross-functional collaboration, with emphasis on quality, compliance, and effective communication with investigators and regulatory bodies.