(Sr.) Clinical Research Manager — Roche
- Location
- Basel
- Contract
- full-time
- Posted
- 3 days ago
Role overview
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.
- 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.
- Main Tasks & Responsibilities:
- Plans and executes local studies includes clinical evaluation, clinical trials and/or research studies primarily for non-approved product registration in China, ensures all clinical studies 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.
Main responsibilities
- Main Tasks & Responsibilities:
- Plans and executes local studies includes clinical evaluation, clinical trials and/or research studies primarily for non-approved product registration in China, ensures all clinical studies 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.
- 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.
- Deliver clearly goals, deadlines and expectations to ensure the project is achieved.
- Provides input to budgets.
- Identifies opportunities to reduce costs.
- May manage portions of larger area(s) budget.
- Support to manages the trial budgets and timelines and accountable for ensuring that budgets and schedules are met.
- Manages internal and external resources to make studies succeed.
- Build up a team and identify the advantages of team members, promote the cooperation of team members advantages.
Application process
- Identify opportunities to simplify and speed up the institution, EC and HGRAC application process
- Be familiar with company and department policies/department regulations and SOPs and understand the business relationships, and have the capacity to innovate
- 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
- Identify new risks in a changing environment and effectively identify and control risks
- Adjust clinical plan according to changes and trends
- Adapt to volatile environments while insist to focus on long-term strategies 10.
- Identify opportunities of cost reduction from a functional team perspective to maximize cost effectiveness 11.
- Provide support, motivate and inspire others to perform at their best
Additional details
- Join Roche, where every voice matters.
- Adapt to volatile environments while insist to focus on long-term strategies
- Identify opportunities of cost reduction from a functional team perspective to maximize cost effectiveness
Notes and original content
- The Position
- Job Summary:
Questions about this listing
What salary does Roche offer for this role?
Roche lists CHF 85'500 - 129'500 gross per year for this position in Basel. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Roche offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Roche during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Basel's cantonal migration office or with HR during the application.
How do I apply for this position at Roche?
Use the "Apply now" button on this page — it links directly to Roche's original listing at roche.wd3.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
