Clinical Operations Study Startup Lead

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The Position

At Roche Pharma Product Development Global Clinical Operations (PDG), we are determined to transform drug development and realize our Pharma Ambition to deliver 20 transformative medicines addressing diseases with the highest societal burden by 2029.

As a key member of our Country Study Start-Up team, you will drive and facilitate the efficient initiation of clinical trials, ultimately helping to deliver innovative treatments to patients. You'll work in a highly collaborative and cross-functional environment, where you have the opportunity to influence and shape our clinical trial delivery strategy. This is a unique opportunity to use your expertise to make a meaningful impact by ensuring seamless trial execution for patients, investigators, and clinical site staff.

The Role

• Lead Country Strategy: You will lead the country strategy for study start-up, driving efficiency, innovation, and collaboration with external stakeholders.

• Oversee Operations: You will oversee start-up operations to ensure timely and efficient site activation and regulatory compliance.

• Drive Process Improvements: You will identify and lead opportunities for process automation, standardization, and innovation at both the country and site levels.

• Collaborate and Harmonize: You will collaborate with regional and global counterparts to harmonize systems and improve timelines.

• Manage Clinical Trial Submissions: You will oversee the development and management of clinical trial submissions and amendments, ensuring regulatory coordination.

• Strategize on Budget & Contracts: You will provide strategic oversight for all aspects of budgeting and contract management, including developing budget strategies and negotiating with internal and external stakeholders.

• Influence the Environment: You will participate in external industry collaborations to influence the country's start-up environment.

Who You Are

• You have a degree (MD, PhD, MA/MS, BA/BS) in life sciences or a related field. A postgraduate degree is highly desirable.

• You have demonstrated experience in clinical trial start-up, regulatory submissions, and cross-functional collaboration.

• You possess a strong understanding of ICH-GCP, EU CTR, and local regulatory environments.

• You have excellent communication, interpersonal, and problem-solving skills, with a collaborative mindset.

• You are fluent in both written and spoken English, and in the language(s) of the host country.

#ClinOps

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.