Meidcal - Clinical Operation Manager - Shanghai

(0315) Sanofi Sp. z o.o.

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Shanghai Until 8/23/2026 8+ years exp H-1B sponsor history First posted June 24, 2026 Last posted June 24, 2026
Job description

 Main responsibilities:

-Provide strategic operation input for data gap analysis and Integrated Evidence Generation Plan (IEGP) for assigned therapy areas as needed.

- Develop clinical study planning according to agreed business priorities.

-Lead medical studies, including Company Sponsored Study (CSS) & External Sponsor Research (ESR), global and local review process.

-Work on overall study execution, including vendor management to make sure on-time delivery of all study key milestones, identify and eliminate potential risks of study delays meet the commitment KPIs with/without CSO.

-Track study status and update monthly performance reports.

-Manage External Sponsor Research (ESR) from proposal/protocol review, contract, study progress follow up and payment, and etc.

-Ensure compliant management of all ISS/CSS status and documents in required systems.

-Liaise with Medical, CSO, and global cross-functional teams to ensure proper planning and execution of medical-funded studies according to business priorities, agreed timelines, and budgets.

-Budget Evaluation & Management: budget evaluations and review, budget transfers and increases, and budget follow-up and identify potential issues and serve as contact person for Controlling, CSU, CSO, global line functions and etc.

-Ensure compliance, governance and risk management of responsible studies, including internal audit, internal control and related activities.

-Support for external key stakeholders’ study operation related communication as need.

-Undertake other tasks as required.

About you

 

Education: Master’s degree in medicine/ biology or above

Experience:

  • 8 years above working experience in pharmaceutical/CRO industry
  • Minimal 4 years of clinical trial management, preferable specialized in medical affaire study, including Company RWE study, ISS and etc.
  • Minimal 2 years CRO experience.
  • independent project management experience with at least 6 projects lasted for 1 year, and with more than five different stakeholders
  • PMP is preferred

Core competencies:

·        Excellent spoken and written English and mandarin

·        Good cross-function coordination and communication skills

  • Influencing, communication
  • Planning and Organising
  • Quality Orientation
  • Building Partnership
  • Initiative and leadership
  • Business Acumen
  • Working under pressure

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About this role

Summary

Manage clinical studies, oversee execution, vendor relations, and ensure compliance.

Job title

Medical - Clinical Operation Manager - Shanghai

Experience level

8+ years

Minimum experience

8+ years exp

Industry

pharmaceutical

Location requirements

Shanghai; remote work not specified.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

clinical trial managementmedical affairsproject managementregulatory compliancecommunication

Preferred skills

CRO experiencePMP

Specializations

clinical trial managementmedical affairsstudy coordinationbudget managementregulatory compliance
Locations

Structured locations inferred from the posting.

Shanghai, China

On-site City