Clinician, Senior Manager

Clinical Trial Execution

• Provide ongoing medical oversight for clinical studies.
• Review clinical data, safety signals, and protocol deviations.
• Support implementation of risk mitigation strategies.
• Ensure studies are conducted in compliance with internal standards, ICH-GCP, and applicable regulations.

Medical Monitoring and Safety Management

• Perform or support medical monitoring activities.
• Review adverse events, emerging safety issues, and patient-level data.
• Participate in Safety Review Plans and Risk Management activities.
• Support Data Monitoring Committees (DMCs) and Endpoint Adjudication Committees.

Data Interpretation and Reporting

• Provide clinical input into SAPs, TLFs, clinical study reports, and related documentation.
• Support interpretation and communication of clinical trial results.
• Ensure scientific rigor and data quality throughout the study lifecycle.

Investigator and Stakeholder Engagement

• Serve as the primary medical/scientific contact for investigators.
• Support investigator meetings and protocol-related discussions.
• Respond to clinical and medical questions from internal and external stakeholders.

Basic Qualifications

MD Clinician

• Medical degree (MD or equivalent).
• Clinical practice and/or drug development experience.
• Strong knowledge of clinical development, safety monitoring, and regulatory requirements.

Non-MD Clinician

• Bachelor's degree or equivalent (advanced degree preferred).
• 4+ years of experience in biopharmaceutical clinical research and development.
• Extensive knowledge of clinical development, global/regional regulations, and ICH-GCP.
• Strong project management and communication skills.

Core Competencies

Medical and Scientific Excellence

• Demonstrated expertise in clinical development and lifecycle strategy.
• Ability to discuss scientific, clinical, regulatory, and commercial considerations.
• Strong disease area knowledge and scientific credibility.

Accountability

• Takes ownership of study deliverables and results.
• Drives execution and achieves key milestones.

Teamwork and Leadership

• Fosters collaboration across functions.
• Supports team success and capability development.
• Demonstrates effective stakeholder management.

Change Agility

• Adapts effectively to changing business and development environments.
• Maintains performance in complex and ambiguous situations.

Typical Scope in Development China

A Clinician (Senior Manager) may lead or support:

• China CTA preparation and submission
• Protocol and amendment development
• Medical monitoring activities
• KOL and investigator engagement
• Clinical data review and interpretation
• CSR and NDA support
• Cross-functional collaboration with Global Study Teams
• China-specific development strategy input

Work Location Assignment: Hybrid

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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Medical