My client a global biotech company who currently have leading products for the treatment of neurodegenerative, hematologic and autoimmune diseases, who also employ over 10,000 professionals worldwide are currently seeking to bring on board a Director of Biostatistics to join their offices in Switzerland. ...
Senior CRA – Freelance position – Italy, Spain and Germany
Senior CRA - Freelance position - Italy, Spain and Germany
We are recruiting for Senior Clinical Research Associates with 5+ years of experience to work in Geneva. This SCRA contract role will take approximately up to 0.5 FTE, and so you will be able to control your hours more as a contractor. As a freelancer you can build your CV with an upcoming company and have more time to plan for yourself.
Clinical Trial Manager
Company:Real Life Sciences Location: South San Francisco Salary: 100,000+ Benefits: negotiable
Closing Date: 14 Oct 14
* Manages the operational aspects of clinical trials * Manages the study project plan, including timeline, budget, and resources * Participates in study strategy development, protocol, CRF development, Clinical Study Report preparation, NDA submission, as appropriate * Prepares metrics and updates for management, as assigned * Proactively identifies potential study issues/risks and recommends/implements solutions * Participates in and fa ...
An innovative medical device consultancy company based in the German speaking part of Switzerland are currently searching for a research and development engineer to join them on the innovation of a new technology. Be part of the future success the role will give you the opportunity to grow within the company and become successful leading to higher work fulfilment.
Are you a Device Engineer looking to work for worldwide specialized consultancy company? This unique opportunity will give you the security of a permanent position but the variety to work on various projects. My client is searching for a Device Engineer to join them on a permanent basis.
Senior Manager Regulatory Advertisement and Promotion
The Associate Director of Strategic Project Management is a pivotal position with high visibility across multiple cross functional areas. This individual is responsible from strategic project management specifically focussed on the transition of compounds from late stage R&D, drawing lead candidates into FTIM studies and early phase development. ...
An exciting position has become available working as a Contract Qualified Person with a global pharmaceutical company based in the South East. This will be responsible for releasing a variety of dosage forms and it will be possible to complete the role on a part time basis.
It is a pre-requisite to be a Qualified Person under the permanent provisions Directive 2001/83/EC.
Our client is a renowned pharmaceutical company with strong pipeline of projects that require an experienced Interim to Project Manage cross functional relationships and assist with the delivery of programs throughout phase I-IV development. ...
**Associate Director GCP/PV Quality - Leading Global Pharmaceutical Company - NEW YORK**
I am working with a Globally recognised and extremely successful pharmaceutical company, based in New York USA, who are actively seeking an Associate Director GCP/PV Quality Assurance and Auditing. The company can offer an excellent salary, benefits, plus they work in some very interesting areas of the industry. This opportunity will ideally suit a Senior Manager/Audit professional who has specialised in GCP and PV for the majority of their career.
**Associate Director GLP Quality Auditing** - Excellent Pharmaceutical Company, NY USA
I am working with a Globally recognised and extremely successful pharmaceutical company, based in New York USA, who are actively seeking an Associate Director GLP Quality Auditing. The company can offer an excellent salary, benefits, plus they work in some very interesting areas of the industry. This opportunity will ideally suit a Senior Manager/Audit professional who has specialised in GLP for the majority of their career.
* Strong skills in embedded software architecture and C programming * Knowledge of real-time operating systems, digital signal processing and digital control * Solid grasp of good hardware and software engineering practices * Proficiency with Verilog or VHDL for FPGA development * Proficiency with Matlab/Simulink and LabView * Track record of getting amazing products to market on time with fantastic innovati ...
Are you a Project Manager with experience within Human Factors? My client a worldwide specialized consultancy company are searching for a Human Factor Project Manager to join them on a permanent basis.
DRA Manager, Great Variety of Products, Commercial Elements
My client is seeking a sales manager to manage the distribution for orthopaedic and dental bio materials to the South East Asian market. This will give you the rare opportunity to network with a unique client base based in Asia.
Furthermore, you will work within a privately owned, family company that offer you with the up most professional support in order for you r to achieve the highest success. ...
The research and development pipeline of my client is one of the best in the industry, with an ever growing R&D budget and a quest to find exemplary professionals to push forward the organisation to continue success, a need for a Interim Drug Safety Physician to work on the cardiovascular and metabolic products has been established.
An internationally successful healthcare company are searching for a Sales Representative to work with their critical care product portfolio across the Central & Eastern part of Switzerland. This position will allow for you to develop and expand a network of KOL's across the Swiss German region and work with a well respected product line of critical care products that already have a strong reputation within the Swiss market.
- Provide statistical input in study protocol (trial design, sample size, randomization and data analysis section) and prepare statistical analysis plans. - Perform statistical analysis and interpret clinical trial data, prepare statistical methods and results sections of the clinical study report and manuscripts. ...
A Global based Consumer Health Company are looking for a Validation Engineer to join their team on an initial 6 month contract. They are looking for someone on a 1.0 FTE basis working in their Midlands office assisting them with their Validation project. The company are willing to pay above market rate for the right candidate.
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