位于中华人民共和国的 20 个优质sr clinical study management职位（正在招聘！）

Responsible for ensuring operational excellence related to clinical trial activities within TCO. Track progress to key quality indicators (KQIs), Quality Plan and overall compliance to applicable processes and regulations. Lead and assist in the development and implementation of process improvement initiatives within the function; ensure changes are adequately communicated and managed.
Work collaboratively with CQA and appropriate line functions to ensure that TCO upholds high quality standards.•Accurate and timely execution of process improvement and quality initiatives as measured by meeting key milestones effectively.
Successful implementation of process improvements as measured by sustainable changes and improved efficiency.
Increased compliance with relevant processes.
Establish business partnerships with all relevant TCO functional groups, CQA, training and other LFs as required.
Training programs implemented in a timely fashion, and tracked to ensure compliance and maintenance

Essential Requirements:

BS or advanced degree in scientific discipline or equivalent education in life science/healthcare required

A minimum of 5 years of relevant pharmaceutical clinical development experience
Extensive knowledge of clinical development process, GCP and clinical quality management; including strong understanding of regulation and guidance for clinical studies
Proficiency/Fluency in English
Experience working in matrix environment and in global teams.
Excellent interpersonal, problem-solving, negotiation and conflict resolution skills
Excellent organizational skills, as well as predisposition to quality management and process improvement
Excellent communicator and presenter (oral and written).

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

Division

Biomedical Research

Business Unit

Research

Location

China

Site

Shanghai (Shanghai)

Company / Legal Entity

CN14 (FCRS = CN014) China Novartis Institutes for BioMedical Research Co., Ltd.

Functional Area

Research & Development

Job Type

Full time

Employment Type

Regular

Shift Work

Accessibility and accommodation

Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

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Summary

About the Role

Key responsibilities:

Accessibility and accommodation

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