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Roche

Global Studies Leader (GSL)

Roche is hiring a Global Studies Leader (GSL) in Shanghai, China. Level rates it ; you can apply on Roche.

Level's read on this job

  • Little AI ●○○○ is how Level rates this role: aI is not part of the work.
  • Tools and skills the posting cites include clinical research, project management and compliance.
  • Level classifies it as a senior role.
  • Level lists 1,200+ other open roles at Roche.

AI in this role

Lead and coordinate cross-functional clinical study teams to ensure clinical studies progress according to plan.

clinical-researchproject-managementcompliance

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

As the Study Management Team Lead, your key responsibilities include:

● Lead and coordinate a cross-functional study team of experts , in compliance with ICH-GCP

and Roche processes in accordance SOPs and guidelines to ensure the clinical study

progresses as planned through driving the achievement of milestones according to

timelines, budget and quality standards

● Provide input into and hold accountability for the development of essential study level

documents (i.e. Clinical Study Protocol, Clinical Study Report) in accordance with relevant

SOPs

● Develop and maintain in collaboration with CRO partners quality risk strategy, relevant

study plans and data to drive clinical study execution and allow adequate oversight

● Accountable and responsible to ensure data entry timeliness and accuracy in our systems,

regardless of who is accountable or responsible for entry of the data

● Lead/facilitate communication across all functions and provide guidance and support to

the core and extended study team members as needed

● Drive innovation in clinical operations by thinking of and contributing to the

implementation of new approaches in partnership with COE, APO and HBS in order to

deliver outcomes that meet and exceed industry best practices.

● Build and role model effective study partnership behaviors and mindsets with your TA

aligned CRO partner to ensure we maximize the expertise of the CRO and our internal

colleagues, minimising duplication of work and ensuring cost and resource efficiency for

study(ies) in responsibility

● Ensure all external service providers (ie, CROs, IXRS, ePRO, etc.) that are engaged at the

study level are delivering to their contractual obligations within the agreed timelines and

budget, and that oversight is documented and issues escalated as appropriate.

● Oversee study level performance against agreed upon plans, milestones and key

performance indicators (KPIs, quality and operational) by using company tracking systems

and proactively communicating any risks to timelines and/or quality, or identified quality

issues, along with proposed mitigations to your Operations Asset Leader and your People

leader

● Oversee Trial Master File (TMF) completion in accordance with relevant SOPs, ensuring QC

activities are performed on an ongoing basis to maintain TMF completeness at all times

● Ensure timely compliance with company-wide governance controls (e.g. Delegation of

Authority, Sunshine Act)

● Develop and oversee the study budget throughout the study lifecycle including budget

re-forecasting, identification of any financial risks and enactment of mitigation plans.

Including proactive communication of financial risk and mitigation plans to the GOAL

● Maintain study inspection readiness at all times, according to ICH-GCP and relevant SOPs,

policies/guidelines and support for asset filings; the GSL is the primary Study

point-of-contact in the event of a study audit or inspection

● Provide study team members and their line managers with regular feedback on their

individual performance to support their professional development and the achievement of

a High Performing Organization

● Work on non-asset project work, such as the Subject Matter Experts (SME) representative

in change initiatives that drive process improvements and/or lead improvement projects as

discussed and agreed upon with their manager

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.


Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

How we rate this

Global Studies Leader (GSL) at Roche rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Clinical ResearchProject ManagementCompliance

Questions you could be asked

  1. Tell me about a project where clinical research was part of your work. What did you do?
  2. Tell me about a project where project management was part of your work. What did you do?
  3. Tell me about a project where compliance was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Clinical Research, Project Management, and Compliance. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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