Clinician – Shanghai/Beijing

About the role

The Clinician will lead clinical studies for a global pharmaceutical client in Shanghai and Beijing. Reporting to the Business Unit, the role combines scientific expertise with operational oversight to ensure high‑quality, efficient trials.

Key responsibilities

• Co‑chair the clinical study team and work collaboratively with all study members.
• Accountable for design, conduct, interpretation and reporting of one or more clinical studies.
• Provide clinical and scientific input to trial strategy and protocol development, including competitor product knowledge.
• Apply Enhanced Clinical Trial Design (ECTD) and Enhanced Quantitative Drug Development (EQDD) to create efficient protocols.
• Draft clinical trial outlines, protocols and amendments with internal and external experts.
• Develop and deliver protocol training materials for site initiation and investigator meetings.
• Establish and oversee Data Monitoring Committees and endpoint adjudication committees.
• Ensure enrollment targets and timelines are met, coordinating with Regional Clinical Site Leads.
• Maintain direct contact with investigative sites to support investigator engagement and enrollment.
• Conduct regular safety reviews, identify emerging trends and coordinate with Medical Monitor.
• Review and manage protocol deviations and ensure data quality throughout the study.

Required profile

• Medical degree (MD, DO, or equivalent) with experience in clinical research.
• Proven track record of leading clinical studies in pharma or CRO environment.
• Strong understanding of clinical trial design, regulatory requirements and safety monitoring.
• Ability to collaborate with cross‑functional teams and external investigators.
• Excellent communication skills in English; Mandarin proficiency preferred.

Required skills

• Enhanced Clinical Trial Design (ECTD)
• Enhanced Quantitative Drug Development (EQDD)
• Protocol writing and amendment management
• Data Monitoring Committee (DMC) oversight
• Safety data review and adverse event management