# Sr. Clinical Research Lead at Roche

Roche is hiring a Sr. Clinical Research Lead in Beijing, China. Level rates it Little AI ●○○○; you can [apply on Roche](https://jobsbylevel.com/go/e0919f63-2353-4233-b4bc-f0353bb5a89b?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Beijing.

## Details

- Company: [Roche](https://jobsbylevel.com/companies/roche)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Beijing
- Posted: August 5, 2026
- Apply: https://jobsbylevel.com/go/e0919f63-2353-4233-b4bc-f0353bb5a89b?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=sr-clinical-research-lead-at-roche-9f1142

## Prepare for this job

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## Description

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 Job Summary: 1. This position provides strategic guidance, oversight, and effective delivery for clinical programs in areas of focus in partnership with cross-functional key stakeholders involved in clinical development. 2. The person may actively participate on cross-functional project teams responsible for the clinical research activities to support Roche Diagnostic China registration of products developed by Roche Group globally, such as, clinical software, instrument platforms, assays, reagents, devices, instruments, systems and biomarkers. Foster cross functional relationships to create a cooperative work environment in support of corporate goals. Ensures alignment across studies and lifecycle teams with current regulatory expectations including ensures compliance with the company SOPs, Policies, Directives, Divisional standards, Declaration of Helsinki, Industry standards, relevant GxPs, both NMPA and/or international requirements and/or best practices. 3. Be familiar with regulatory requirements and understand regulatory trends and the impact on the project. 4. Be familiar with company and department policies/department regulations and SOPs and understand the business relationships, and have the capacity to innovate 5. Be familiar with the product characteristics, guidance and consensus of relevant experts in the field of the research project, and provide key suggestions for the protocol design. 6. Expertise in clinical pathways and performance metrics; skilled in the independent development of rigorous clinical study reports and academic publications. 7. Provide strategies for clinical studies, including clinical evaluation, clinical trials and/or other clinical projects. 8. Identify new risks in a changing environment and effectively identify and control risks. 9. Adjust clinical plan according to changes and trends. 10. Adapt to volatile environments while insisting on long-term strategies. 11. Identify opportunities of cost reduction from a functional team perspective to maximize cost effectiveness. 12. Provide support, motivate and inspire others to perform at their best performance. Main Tasks & Responsibilities : 1. Plans and executes local studies includes clinical evaluation, clinical trials and/or other studies primarily for non-approved product registration in China and/or may support regulatory registration elsewhere. 2. Responsible for the implementation and support maintenance of the clinical trial-related policies, as well as processes and procedures related to the Design Control requirements. 3. Deliver clearly goals, deadlines and expectations to ensure the project is achieved. 4. Provides input to budgets. Identifies opportunities to reduce costs. May manage portions of a larger area(s) budget. 5. Manages the trial budgets and timelines and is accountable for ensuring that budgets and schedules are met. 6. Manages internal and external resources to make studies succeed. 7. Skilled in using clinical strategies and performance specs to develop rigorous study reports and high-level academic literature. 8. Build up a team and identify the advantages of team members, promote the cooperation of team members advantages. Ensure that the goals and activities of your work or project team are aligned with regional and company goals. And discover the needs of team members in solving problems, and guide them to better understand and solve problems correctly. 9. Build up effective communication methods to manage project members/teams and support and

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