Physician – Clinical Monitoring (Shanghai)

About the role

We are seeking an experienced Physician to join our clinical research team in Shanghai. The role focuses on medical monitoring and pharmacovigilance support for sponsor‑led studies, ensuring safety and scientific integrity throughout the trial lifecycle.

Key responsibilities

• Participate in study planning, feasibility assessments and investigator meetings.
• Provide training on therapeutic area indications and study protocols to study teams.
• Review and sign off clinical data listings, tables, protocol deviations and datasets for medical accuracy.
• Deliver medical monitoring activities according to the Medical Monitoring Plan, including answering site queries and assessing safety data.
• Support risk assessment, safety reporting and pharmacovigilance workflows for assigned trials.
• Engage with sponsors on project challenges, client satisfaction metrics and remediation actions.
• Participate in audits, inspections and on‑call rotations for emergency medical contact and unblinding requests.

Required profile

• Medical degree (MD or equivalent) with clinical experience.
• Strong knowledge of clinical trial conduct, medical monitoring and pharmacovigilance processes.
• Excellent communication skills to interact with sponsors, investigators and internal teams.
• Ability to work under tight timelines and identify risks proactively.

Required skills

• Medical monitoring and safety assessment.
• Clinical protocol review and documentation.
• Pharmacovigilance workflow understanding.

What we offer

• Opportunity to work on global clinical studies with a leading CRO.
• Collaborative environment with multidisciplinary teams.
• Professional development and training in therapeutic areas.