Development at Roche – A place for pioneers
Are you looking for a chance to use new ideas, build your career, and improve lives, all at the same time? If you have a passion for innovation, research and development, come and join Roche and see how your contribution can make a real difference to patients all around the world.
Thanks to the expertise and experience of our two primary corporate divisions, Diagnostics and Pharmaceuticals, Roche is able to take advantage of countless synergies in the field of research and development. Our efforts are further supported by a variety of technical co-operations and a network of alliance partners that help us to promote the development of individual products or product portfolios. We rely on innovative and committed individuals like you to succeed in these endeavours.
We invite you to choose a career in the field of development at Roche, and profit from our proven network of innovation, research and development – regardless of whether you’re at home in the field of clinical science, biology, biochemistry, biotechnology, chemistry or pharmacy.
Headquarter sites for the Roche Pharma Development (PD) function are located in Switzerland, the United States, UK and China. In addition, the function has a strong presence in Australia, France, Canada, Spain and many more countries around the world. Roche Pharma Development has also entered co-development partnerships with Genentech (USA) and Chugai (Japan), jointly developing a variety of groundbreaking products to improve lives.
Roche’s Parma Development sector is subdivided into the following key areas:
Medical Science
PD Medical Science provides high-quality scientific and medical expertise to the development effort. Medical Science is split into two functions – Clinical Research & Exploratory Medicine / Clinical Development - and is the home of clinical science, clinical pharmacology, biomarkers, translational medicine as well as early stage study management and data management. In Medical Science you can either assume a responsibility at the interface between Research and Development, or take a position around the development and execution of clinical development plans.
Operations
PD Operations is the home of clinical study management, clinical study monitoring and data management resources within Roche Pharma Development. In Operations, you’ll assume responsibility for the planning and implementation of high-quality clinical programmes that meet specific scientific, medical, magisterial and commercial requirements.
Regulatory Affairs
PD Regulatory Affairs supports the Research and Development Teams, LifeCycle Teams and “mature products” group. In PD Regulatory Affairs, you will develop and implement regulatory strategies for global registration and for the ongoing maintenance and issue management of Roche products.
Safety Risk Management
PD Safety has the responsibility to protect patient’s safety. In PD Safety you will produce safety surveillance plans, evaluate signals and adverse events, and initiate risk management activities.
Quality Assurance
In PD Quality Assurance you will assist the Pharma Division in achieving and maintaining high quality standards in clinical development, trial systems and processes.
Methodology & Innovation
In PD Methodology & Innovation, you will provide analytic solutions to maximize the success of the development efforts. Amongst other professions, biomathematicians, biostatisticians and pharmacometricians find their home in Methodology & Innovation.
The functions above are supported by PD Project Management and PD Central Services and with regards to project management and resource planning, compliance, training and knowledge sharing.
Our Diagnostics Division works continually to maintain a leading market position in the management of healthcare information. It integrates diagnostic test results and medical information in order to support physicians and facilitate optimum administration of their patients. By joining these efforts, you can make a contribution to the quality of life of people all around the globe by applying your expertise and experience where it is needed most.
The development areas of our Diagnostics Division include:
• Advanced Technology
• Blood Screening
• Core Chemistry
• Development Administration
• Design Control Documentation
• Genomics, Microbiology
• Systems Integration
• Virology
• Women’s Health
Currently we are particularly interested in the following positons:
Our range of job offers in these areas provides you with an unmatched overview of these critical fields of activity.
Thanks to the expertise and experience of our two primary corporate divisions, Diagnostics and Pharmaceuticals, Roche is able to take advantage of countless synergies in the field of research and development. Our efforts are further supported by a variety of technical co-operations and a network of alliance partners that help us to promote the development of individual products or product portfolios. We rely on innovative and committed individuals like you to succeed in these endeavours.
We invite you to choose a career in the field of development at Roche, and profit from our proven network of innovation, research and development – regardless of whether you’re at home in the field of clinical science, biology, biochemistry, biotechnology, chemistry or pharmacy.
Headquarter sites for the Roche Pharma Development (PD) function are located in Switzerland, the United States, UK and China. In addition, the function has a strong presence in Australia, France, Canada, Spain and many more countries around the world. Roche Pharma Development has also entered co-development partnerships with Genentech (USA) and Chugai (Japan), jointly developing a variety of groundbreaking products to improve lives.
Roche’s Parma Development sector is subdivided into the following key areas:
Medical Science
PD Medical Science provides high-quality scientific and medical expertise to the development effort. Medical Science is split into two functions – Clinical Research & Exploratory Medicine / Clinical Development - and is the home of clinical science, clinical pharmacology, biomarkers, translational medicine as well as early stage study management and data management. In Medical Science you can either assume a responsibility at the interface between Research and Development, or take a position around the development and execution of clinical development plans.
Operations
PD Operations is the home of clinical study management, clinical study monitoring and data management resources within Roche Pharma Development. In Operations, you’ll assume responsibility for the planning and implementation of high-quality clinical programmes that meet specific scientific, medical, magisterial and commercial requirements.
Regulatory Affairs
PD Regulatory Affairs supports the Research and Development Teams, LifeCycle Teams and “mature products” group. In PD Regulatory Affairs, you will develop and implement regulatory strategies for global registration and for the ongoing maintenance and issue management of Roche products.
Safety Risk Management
PD Safety has the responsibility to protect patient’s safety. In PD Safety you will produce safety surveillance plans, evaluate signals and adverse events, and initiate risk management activities.
Quality Assurance
In PD Quality Assurance you will assist the Pharma Division in achieving and maintaining high quality standards in clinical development, trial systems and processes.
Methodology & Innovation
In PD Methodology & Innovation, you will provide analytic solutions to maximize the success of the development efforts. Amongst other professions, biomathematicians, biostatisticians and pharmacometricians find their home in Methodology & Innovation.
The functions above are supported by PD Project Management and PD Central Services and with regards to project management and resource planning, compliance, training and knowledge sharing.
Our Diagnostics Division works continually to maintain a leading market position in the management of healthcare information. It integrates diagnostic test results and medical information in order to support physicians and facilitate optimum administration of their patients. By joining these efforts, you can make a contribution to the quality of life of people all around the globe by applying your expertise and experience where it is needed most.
The development areas of our Diagnostics Division include:
• Advanced Technology
• Blood Screening
• Core Chemistry
• Development Administration
• Design Control Documentation
• Genomics, Microbiology
• Systems Integration
• Virology
• Women’s Health
Currently we are particularly interested in the following positons:
- Translational Medical Leader
- Biomarket experimental Leader / Scientist
- Pharmacometrics
- Clinical Scientist / Scientist Leader
- Pathologist
- Toxicologist
- Health Economist
- Principal Scientist - R&D (Electrochemistry)
- Manager - Clinical Trials
- Regulatory Affairs
Our range of job offers in these areas provides you with an unmatched overview of these critical fields of activity.
100 jobs for the selection "Development"
| Date | Job | Job Type | Site |
|---|---|---|---|
| 11/20/09 | Early Development External Collaborations Business Analyst | Standard | United States - New Jersey - NutleyUnited Kingdom - England - Hertfordshire (Welwyn)Switzerland - Basle-Town - Basle |
| 11/18/09 | Bilingual Drug Information Intern | Standard | Canada - Ontario - Meadowpine - Head Office |
| 11/17/09 | Senior Program Manager - Drug Regulatory Affairs | Standard | United States - New Jersey - Nutley |
| 11/17/09 | Bilingual Drug Information Associate | Standard | Canada - Ontario - Meadowpine - Head Office |
| 11/16/09 | GERENTE MEDICO ONCOLOGIA | Standard | Ecuador - Quito - Quito |
| 11/16/09 | temporary Clinical Science Specialist | Fixed Term | Switzerland - Basle-Town |
| 11/16/09 | Stagiaire assistant Médecin chef de projet - H/ F | Internship /Industrial Placement | France - Île-de-France - Neuilly-sur-Seine (92) |
| 11/16/09 | Ingenieur Biotechnologie (m/ w), Standort Penzberg | Fixed Term | Germany - Bayern - Penzberg |
| 11/16/09 | Stagiaire Statisticien - H/ F | Internship /Industrial Placement | France - Île-de-France - Neuilly-sur-Seine (92) |
| 11/16/09 | Manager Senior, Companion Diagnostics Development (IRC9794) | Standard | United States |
| 11/16/09 | Manager, Workflow Consulting (IRC12156) | Standard | United States - Arizona - Tucson |
| 11/16/09 | Manager, Workflow Consulting (IRC12156) | Standard | United States - Arizona - Tucson |
| 11/16/09 | Pathologist, Staff (IRC12136) | Standard | United States - Arizona - Tucson |
| 11/16/09 | Senior VP, Product Development (IRC11653 | Standard | United States - Arizona - Tucson |
| 11/13/09 | Clinical Science Specialist - Inflammation | Standard | United Kingdom - England - Hertfordshire (Welwyn) |
| 11/13/09 | Clinical Site Manager III | Standard | United States - CA - South San Francisco |
| 11/13/09 | Study Support Principal Mgr | Standard | United States - CA - South San Francisco |
| 11/12/09 | Senior R&D Scientist - Human Factors | Standard | United States - Indiana - Indianapolis |
| 11/12/09 | Global Study Associate (PDY) | Standard | China - Shanghai - Shanghai |
| 11/12/09 | Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 11/11/09 | Director, Regulatory Affairs, Asia-Pacific Region ( PDY) | Standard | China - BeijingChina - Shanghai - Shanghai |
| 11/11/09 | Program Manager - Drug Regulatory Affairs | Standard | United States - New Jersey - Nutley |
| 11/11/09 | Clinical Pharmacology Scientist | Standard | United Kingdom - England - Hertfordshire (Welwyn) |
| 11/11/09 | Assoc Dir, Med Science Liaison | Standard | United States - CA - South San Francisco |
| 11/10/09 | Clinical Research Associate - Medical Marketing - 12 month fixed term contract - Sydney based | Standard | Australia - New South Wales - Dee Why |
| 11/10/09 | Clinical Research Associate - Medical Marketing - 12 month contract - Perth based - Full time or Part time | Standard | Australia - Western Australia - Perth |
| 11/10/09 | Regulatory Records and Information Specialist | Standard | Switzerland - Basle-Town - Basle |
| 11/10/09 | Assoc Scientist (Toxicology) | Standard | United States - CA - South San Francisco |
| 11/09/09 | Clinical Science Leader - Oncology | Standard | United Kingdom - England - Hertfordshire (Welwyn)Switzerland - Basle-Town - Basle |
| 11/09/09 | Senior Systems Engineer | Standard | United States - California |
| 11/09/09 | Sr Business Sys Analyst | Standard | United States - CA - South San Francisco |
| 11/06/09 | Coordinateur d'études Pharmaco-épidémiologiques - H/ F | Fixed Term | France |
| 11/06/09 | Manager, Dev Sci Mgmt | Standard | United States - CA - South San Francisco |
| 11/06/09 | Sr Scientist Drug Safety (MD) | Standard | United States - CA - South San Francisco |
| 11/05/09 | Senior Clinical Scientist - Inflammation | Standard | United Kingdom - England - Hertfordshire (Welwyn) |
| 11/03/09 | Global Marketed Products Program Manager or EU Marketed Products Program Manager | Standard | United Kingdom - England - Hertfordshire (Welwyn)Switzerland - Basle-Town - Basle |
| 11/03/09 | Global Regulatory Leader / EU Partner | Standard | United Kingdom - England - Hertfordshire (Welwyn)Switzerland - Basle-Town - Basle |
| 11/02/09 | Diplomarbeit: Methoden u. Techniken zur Bestimmung der Aktivität u. Konzentration von Enzymen für SMBG-Systeme | Internship /Industrial Placement | Germany - Baden Württemberg - Mannheim |
| 11/02/09 | RSG Coordinator | Standard | Switzerland - Basle-Town - Basle |
| 11/02/09 | Research Asst | Standard | United States - CA - South San Francisco |
| 11/01/09 | Biostatistiker (m/ w) | Standard | Germany - Bayern - Penzberg |
| 10/30/09 | Clinical Scientist - Oncology | Standard | United Kingdom - England - Hertfordshire (Welwyn) |
| 10/28/09 | Clinical Pharmacology Scientist/ Inflammation | Standard | United States - New Jersey - Nutley |
| 10/28/09 | Clinical Pharmacology Scientist Oncology | Standard | United States - New Jersey - Nutley |
| 10/28/09 | Associate Director Clinical Pharmacology Inflammation | Standard | United States - New Jersey - Nutley |
| 10/28/09 | Clinical Pharmacology Scientist Virology | Standard | United States - New Jersey - Nutley |
| 10/28/09 | Associate Clinical Director CRED Oncology | Standard | United States - New Jersey - Nutley |
| 10/28/09 | Clinical Science Specialist CRED Oncology | Standard | United States - New Jersey - Nutley |
| 10/27/09 | Scientist/ Senior Scientist, FACS Assays (MML) | Standard | United States - New Jersey - Nutley |
| 10/27/09 | Medical Marketing Manager | Standard | Switzerland - Zug - Rotkreuz |
| 10/27/09 | Drug Regulatory Affairs Specialist | Standard | Czech Republic - Praha - Praha |
| 10/27/09 | Medical Science Liaison II | Standard | United States |
| 10/27/09 | Medical Science Liaison II | Standard | United States |
| 10/26/09 | Medical Science Liaison II | Standard | United States |
| 10/22/09 | Clinical Pharmacologist (PDZ) | Standard | China - BeijingChina - Shanghai - Shanghai |
| 10/22/09 | Scientist Drug Safety (MD) | Standard | United States - CA - South San Francisco |
| 10/21/09 | Assoc. Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/20/09 | Assoc Grp Med Dir (MD) | Standard | United States - CA - South San Francisco |
| 10/19/09 | KOL Collaborations Leader | Standard | Switzerland - Basle-Town - Basle |
| 10/15/09 | Medical Manager (Oncology) | Standard | Russia - Moscow and Moscow Region - Moscow |
| 10/15/09 | Asst./ Clinical Research Associate | Standard | Taiwan - Taipei |
| 10/14/09 | CRED Clinical Database Programmer | Standard | United States - New Jersey - Nutley |
| 10/14/09 | Assoc. Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/14/09 | Assoc. Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/14/09 | Assoc. Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/14/09 | Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/14/09 | Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/14/09 | Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/14/09 | Sr Dir, Clinical Operations | Standard | United States - CA - South San Francisco |
| 10/13/09 | Asst. Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/13/09 | Asst. Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/13/09 | Asst. Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/13/09 | Group Medical Director(MD) | Standard | United States - CA - South San Francisco |
| 10/13/09 | Lead Statistical Scientist | Standard | United States - CA - South San Francisco |
| 10/13/09 | Senior Biostatistician | Standard | United States - CA - South San Francisco |
| 10/13/09 | Sr Medical Science Liaison | Standard | United States - CA - South San Francisco |
| 10/10/09 | BioSpecimen Acquisition Manager | Standard | United States - California - Pleasanton |
| 10/08/09 | Program Manager - Drug Regulatory Affairs | Standard | United States - New Jersey - Nutley |
| 10/08/09 | Clinical Research Early Development Study Leader | Standard | United States - New Jersey - Nutley |
| 10/08/09 | CRED Study Manager | Standard | Switzerland - Basle-Town - Basle |
| 10/08/09 | CRED Study Leader | Standard | Switzerland - Basle-Town - Basle |
| 10/08/09 | Sr Research Assoc | Standard | United States - CA - South San Francisco |
| 10/07/09 | CRED Study Manager | Standard | United Kingdom - England - Hertfordshire (Welwyn) |
| 10/07/09 | CRED Study Leader | Standard | United Kingdom - England - Hertfordshire (Welwyn) |
| 10/07/09 | Medical Director (MD) | Standard | United States - CA - South San Francisco |
| 10/07/09 | Sr HC Economist | Standard | United States - CA - South San Francisco |
| 10/05/09 | Senior Program Manager - Drug Regulatory Affairs | Standard | United States - New Jersey - Nutley |
| 10/05/09 | Program Manager Drug Regulator Affairs - Advertising & Promotion Marketed Products | Standard | United States - New Jersey - Nutley |
| 10/01/09 | Senior Program Manager - Drug Regulatory Affairs | Standard | United States - New Jersey - Nutley |
| 10/01/09 | Sr Project Manager | Standard | United States - CA - South San Francisco |
| 09/30/09 | Director Compliance Pharma Development Regulatory | Standard | United States - New Jersey - Nutley |
| 09/30/09 | Associate Regulatory Intelligence - Pharma Development Regulatory | Standard | United States - New Jersey - Nutley |
| 09/30/09 | Associate Director - Drug Regulatory Affairs | Standard | United States - New Jersey - Nutley |
| 09/30/09 | Assoc Dir, Clinical Affairs | Standard | United States - CA - South San Francisco |
| 09/29/09 | Global Studies Leader, Study Management (PDY) | Standard | China - Shanghai - Shanghai |
| 09/29/09 | Scientist - Pathology | Standard | United States - CA - South San Francisco |
| 09/28/09 | Manager, Clinical Data Mgmt | Standard | United States - CA - South San Francisco |
| 09/28/09 | Sr Medical Science Liaison | Standard | United States - CA - South San Francisco |
| 09/25/09 | Sr Clinical Data Coord | Standard | United States - CA - South San Francisco |
| 09/25/09 | Sr Statistical Programmer Ayst | Standard | United States - CA - South San Francisco |