Posted 21 May, 2026

Job Id: 626870

Senior Clinical Data Manager – Beijing/Shanghai


Location: N/A, Beijing
Category: Data Sciences
Salary: Apply for details
Country: China
Employment: Direct Hire/Perm
Worksite: On-Site
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Job Description

We’re working with an innovative, fast-growing global CRO that is transforming how clinical research is delivered. By combining scientific expertise, advanced data capabilities, and clinical execution, they support the development of life-changing therapies worldwide.

As part of their continued expansion across Asia-Pacific, they are now seeking a Senior Clinical Data Manager to join the team.

The Role

This is a senior, hands-on position where you will lead clinical data management activities across multiple studies, from start-up through to database lock. Acting as the key point of contact for data, you’ll ensure high-quality delivery, manage timelines, and collaborate closely with sponsors, vendors, and cross-functional teams.

You will be involved in database design and review, data cleaning, query management, and oversight of documentation and regulatory compliance. The role also offers the opportunity to contribute to process improvements, mentor team members, and support broader business initiatives where needed.

Key Skills & Experience

  • Strong background in clinical data management within a CRO or similar environment
  • Proven experience leading studies end-to-end, from start-up through database lock
  • Solid understanding of clinical trial processes and data management best practices
  • Hands-on experience with EDC systems such as Medidata Rave and/or Veeva
  • Ability to manage multiple studies, timelines, and stakeholders effectively
  • Excellent communication skills, both written and verbal
  • High attention to detail with strong analytical and problem-solving skills
  • Confident working cross-functionally with internal teams, sponsors, and vendors
  • Leadership capability, with experience supporting or mentoring others

Desirable:

  • Knowledge of CDISC standards (CDASH, SDTM, ADaM)
  • Experience with medical coding (MedDRA, WHODrug)
  • Academic or professional background in life sciences, healthcare, or similar
  • Exposure to oncology or rare disease studies
  • Background in Biostatistics

This is a fantastic opportunity to join a forward-thinking organisation during an exciting period of global growth and play a key role in delivering impactful clinical research.

Equal Opportunity Employer

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

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