Student Placement pRED Clinical Operations

F. Hoffmann-La Roche AG; Welwyn; On-site; GBP 12,000 - 18,000; Full time

Job summary

Roche Products Ltd. in Welwyn Garden City is looking for a Clinical Operations Intern to join a multidisciplinary team supporting early phase studies.

You will help with logistics, documentation, trial master files, tracking systems, and coordinating meetings with investigators and vendors. You're in the penultimate or final year of your studies, possess strong planning, organizational and communication skills, and enjoy working in a collaborative environment.

Qualifications

• Penultimate or final year of study.
• Strong planning and organizational skills.
• Good communication and collaborative mindset.
• Awareness of your strengths and development areas.

Responsibilities

• Provides logistical support to a multi-disciplinary team which oversees early phase clinical study activities across a range of disease therapeutic areas.
• Develops, maintains and manages appropriate study documentation.
• Sets-up and maintains Trial Master Files in accordance with Standard Operating Procedure requirements.
• Organizes and maintains tracking systems and tools to support the clinical study from planning through to post close-out activities.
• Coordinates communication of tracking information within the multidisciplinary team and to the study sites as required.
• Manages and tracks: clinical / non-clinical supplies patient recruitment study metrics.
• Coordinates and manages meetings with investigator sites, site monitor’s, including preparing meeting materials and coordinates and manages meetings with service providers/vendors.
• Collaborates with Study Leaders on the development of study-specific plans and/or processes.
• Supports pRED Clinical Operations Clusters on activities related to remit of the group in support of our north star.
• May support departmental initiatives.
• May support Welwyn site-wide initiatives, thereby collaborating across different functional departments.

Skills

Planning

Organization

Communication

Teamwork

Adaptability

Job 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 pRED CLINICAL OPERATIONS

We aspire to be a leading edge Clinical Operations organization that drives innovative patient inclusive approaches in study design and execution, utilizes advanced analytics to make data-driven decisions, and embeds innovative technologies into our ways of working to deliver programs and studies which in turn support delivering on our North Star to increase R&D Productivity and Patient inclusivity. We strive to create a workplace where team members own their own development and learning and are empowered to create and innovate.

The Opportunity Clinical Operations Intern

Students joining Roche will work as part of multi-disciplinary teams to support development and execution of operational strategies to recruit/retain patients and manage study data for early phase clinical studies worldwide.

The intern will be involved in the following activities:

• Provides logistical support to a multi-disciplinary team which oversees early phase clinical study activities across a range of disease therapeutic areas
• Develops, maintains and manages appropriate study documentation
• Sets-up and maintains Trial Master Files in accordance with Standard Operating Procedure requirements
• Organizes and maintains tracking systems and tools to support the clinical study from planning through to post close-out activities.
• Coordinates communication of tracking information within the multidisciplinary team and to the study sites as required
• Manages and tracks: clinical / non-clinical supplies patient recruitment study metrics
• Coordinates and manages meetings with investigator sites, site monitor’s, including preparing meeting materials and coordinates and manages meetings with service providers/vendors
• Collaborates with Study Leaders on the development of study-specific plans and/or processes
• Supports pRED Clinical Operations Clusters on activities related to remit of the group in support of our north star.
• May support departmental initiatives
• May support Welwyn site-wide initiatives, thereby collaborating across different functional departments

Who you are:

• Applicants should be in the penultimate or last year of study, at the “Year in Industry” junction of their studies
• Strong planning and organizational skills and the ability to manage multiple priorities at the same time
• Good communication skills, be supportive and inclusive of a collaborative working environment
• Professional, reliable, and team-orientated outlook
• Supportive and inclusive mindset, and be capable of demonstrating behaviours to work successfully in a collaborative working environment
• Awareness of your strengths and development areas
• Ability to come into the office for the majority of the time as well as being proficient in working in a virtual global setting when required

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.

The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd.

At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment.

All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age.

We recognise the importance of flexible working and will review all applicants’ requests with care.

At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.

We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future.

We are passionate about transforming patients’ lives.

We are courageous in both decision and action.

And we believe that good business means a better world.

That is why we come to work each day.

We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all.

We do this today to build a better tomorrow.

We are proud of who we are, what we do, and how we do it.

We are many, working as one across functions, across companies, and across the world.

We are Roche.

Unfortunately visa sponsorship is not available for this role. Candidates must already hold valid authorisation to work in the UK.

Application deadline: Friday 30th Oct 2026

Final Assessment Center at Roche UK head office (Welwyn Garden City, Hertfordshire). Expected date: 7th December 2026