Medical - Associate Clinical Operation Manager - Shanghai

Job title: Associate Clinical Operation Manager

Division/Business Unit: Greater China Pharma Medical

Location: Shanghai

Report to: Medical Lead of study and publication

About the job

Main responsibilities:

--Provide strategic operation input for data gap analysis and Independent Expert Group Program (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: Bachelor’s degree in medicine/ biology or above, master’s degree is preferred

Experience:

• 3-5 years above working experience in pharmaceutical/CRO industry

• Have the following experience is preferable:

• 2 years of clinical trial management, preferable specialized in medical affaire study, including Company RWE study, ISS and etc.

• independent project management experience with at least 4 projects lasted for 1 year, and with more than five different stakeholders

Core competencies:

• independent project management experience with at least 4 projects lasted for 1 year, and with more than five different stakeholders

·        Good cross-function coordination and communication skills

• Planning and Organising

• Quality Orientation

• Business Acumen

• Working under pressure

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team. ·

• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention, and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!