Our Graduate and Postgraduate opportunities are for those who have recently graduated (0-2 years) from their degrees (Undergraduate, Masters, PhD), and want to take their first steps within industry.
Our Research and project based opportunities are available for those wanting to continue research, such as Postdoctoral Fellowships or collaboration on final year projects (such as dissertation projects).
Graduates (Bachelors, Masters & PhD)
Regulatory Affairs work cross functionally with clinical trail teams to formulate sumbmission for our products, in therapy areas across Onoclogy, Neoroscicence, Immunonogy, Infectious deasiases, & Ophthalmology.
As part of this programme you will gain insight into the work of Regulatory professionals who are responsible for providing the Regulatory input and leadership throughout the life cycle of the product, from initial first-in-human trials all the way to the point at which the product lifecycle comes to an end.
The projects you will work on are real and you will be generating genuine added value.
To broaden your experience across the development value chain you will also have the opportunity to go for a 6-month rotation in another Product Development function.
Putting patients at the forefront of everything we do, we bring our medical and scientific expertise including therapy knowledge to our customer partnerships, ensure access to our products and clinical trials and attend diligently to patient safety and customer enquiries.
In this programme you will participate in development and implementation of the global Medical Information strategy for the assigned therapeutic area/products and/or cross-portfolio activities.
You will support development and delivery of medical information, tools, resources and training so that scientifically accurate, objective and current responses to product enquiries from healthcare professionals (HCPs) and other Roche Pharma customers are consistently provided in a professional, ethical and timely manner.
The digitalisation of healthcare has created a direct link between information technology and patients. In the Roche Start IT programme, you can explore all corners of the field – maybe even surprising yourself with new interests – while making a difference to people’s lives.
As a part of the programme you will get exposure to IT core processes as well as our Pharma and/or Diagnostics R&D, Commercial and Corporate Functions business.
Product Development Clinical Science specializes in late stage clinical development of molecules, conducting primarily Phase III clinical trials with a goal of characterizing the efficacy and safety profile of a molecule in a specific disease area. The priority of Product Development Clinical Science is to ensure that benefit outweighs risk and we are developing medications that are serving patients with an unmet treatment need. Product Development Clinical Science are involved in key stages of a clinical trial such as study design, start-up, maintenance and final analysis phases.
The purpose of the two year programme is to provide a recent PhD or PharmD graduate (completed or due to complete their post-graduate academic studies) with the opportunity to gain specialized, in-depth training and experience in global drug development.
We combine our strengths in pharmaceuticals and diagnostics to better fit treatments to patients. When genetic differences can be identified, the efficacy and safety of medicines can be improved enormously. To this end we have a companion diagnostic strategy for every molecule we develop.
Our Personalised Healthcare (PHC) Data Science programme, take place at our Headquarters in Basel, Switzerland or at Roche UK Affiliate in Welwyn, United Kingdom for a period of 24 months.
Working side by side with other data scientists to help uncover answers to challenging clinical and business questions.The programme encourgaes work across innovative projects spanning multiple disease areas leveraging large amounts of healthcare data originating from EMRs (Electronic Medical Records), Disease Registries, Clinical Trials, Insurance Claims, Digital Health, Genomics and Imaging.
In the biopharmaceutical industry, each data point is part of a patient's story and their contribution to developing better medicines and understanding disease. It is our responsibility to maximize the use of this data for answering new questions and enabling larger-scale analyses for generating new insights.
You will work as part of a team to deliver data and insights about our medicines and to provide solutions that aid the collection, databasing and analysis of clinical trial data for medicines in Roche’s diverse pipeline.
Full training in systems, software and programming will be provided for all roles and you will have frequent access to senior staff that provide coaching and oversight on a day-to-day basis.
Internally known as RPF, this programme aims to build scientific leadership by expanding and strengthening our scientific exchange and collaboration with academia.
Specifically, we offer talented Postdoctoral graduates the opportunity to join us as fellows working on a specific topic, co-mentored by people inside Roche and from external research institutions.
The Patient Centered Outcomes Research (PCOR) vision is: To provide evidence that improves lives through patient-focused outcomes. We achieve this by developing measurement strategies that integrate the patient perspective into drug development.
The patient viewpoint is increasingly important in drug approval and reimbursement decisions as health authorities, payers, patients, caregivers and healthcare providers seek additional evidence of treatment benefit.
This placement will give you the opportunity to be a part of a team that works on collection of clinical outcomes assessments (COAs) such as patient reported outcome (PRO), clinician-reported outcomes (ClinRO), observer-reported outcome (ObsRO), and performance outcome (PerfO) measures, to capture the patient experience while to better understand patients’ perspective of treatment and disease burden.
In Personalized Healthcare, we leverage real world healthcare data and appropriate analytical techniques to identify the right drug for the right patient at the right time, in order to maximise the value of our products for patients, and for the business.
In Biostatistics, as strategic partners in drug development, we apply our drug development and statistical expertise to the design of clinical development plans, clinical studies, and non-clinical experiments.
As an intern, you will have access to both groups, gaining exposure to individuals with expertise across the development pipeline and in both real world and clinical trial data. This is an excellent opportunity to gain hands-on experience by working on a specific pharmaceutical projects.
In the biopharmaceutical industry, each data point is part of a patient's story and their contribution to developing better medicines and understanding disease. It is our responsibility to maximize the use of this data for answering new questions and enabling larger-scale analyses for generating new insights.
Data Science placement students will work as part of a team to deliver data and insights about our medicines and to provide solutions that aid the collection, databasing and analysis of clinical trial data for medicines in Roche’s diverse pipeline.
During this programme you will work under the supervision of experienced biostatisticians on theoretical or applied problems with direct relevance to Roche’s ongoing clinical drug-development research in areas such as oncology, immunology, infectious disease, ophthalmology, and neuroscience.
Find out more Graduate opportunities in Europe
Graduates Are you about to complete your Bachelor’s or Master's degree, are you looking for a PhD position, or has your PhD thesis been defended and are you looking for a post-doctoral position? Whether in a trainee or post-doc program or as a direct entrant, together we can ensure a successful start to your career.
