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.
The ideal profile will; â€¢ Have over four years experience in clinical research from either a Pharmaceutical, Biotech or CRO environment â€¢ Must have a solid background in Study Management â€¢ Knowledge in ICH-GCP and proven experience in EC submissions and contract negotiations is essential
This opportunity offers a competitive daily rate, in return for 6 months full time commitment as a Freelancer. ...
Global Director of Pharmacovigilance/Drug Safety â€“ Fast-growing mid-sized CRO â€“ Scotland, UK
Global Director of Pharmacovigilance/Drug Safety: This is a fantastic opportunity for someone with strong experience in pharmacovigilance/drug safety to join an emerging CRO in a leadership position. You will be overseeing a global pharmacovigilance team and taking a principal role in building client relationships and bid proposals.
Project Manager-Full Product Life Cycle-Devices-Switzerland
An exciting role to work across the full product life cycle of a world leading medical device company has come in within the greater Zurich area. This is a great opportunity to work with innovative medical devices, working from research and development through to quality and regulatory affairs. Through this full life cycle role you will gain a varied role where you will gain invaluable expertise across a great deal of cross-function work. Apply today to find out more.
Interested in working with a smaller biotech? I am currently working with exactly that. They are looking for an experienced clinical operations director who would be interested in coming on board and spearheading their Oncology trials. This role is a freelance position initially for 6 months, however this is highly likely to extend. You will also need to be hands on and based in Switzerland for this opportunity. ...
This is a great new opportunity with a growing medical device company based in the Geneva area to work in an interesting administration role. Our client are looking for an office manager to work on the day to day running of the business; from organising all administration documentation to meeting and event set up. You will gain a great deal of autonomy in this role and will directly be in charge of the daily operations.
This position will be responsible for the management of all aspects of clinical trials from phase I-IV, including leading a clinical trial team within a specific therapy area, potentially Haematology and Oncology. The incumbent will have program level activities assigned, therefore an candidate with an operational excellence background is desired. ...
Clinical Project Lead / Industry Leading Company / Basel
I am recruiting for a Clinical Project Lead to join one of the industries global giants. My client is looking for someone with direct experience of Near Patient Testing, Project Management experience and who thrives in a culture of success. The position is with an industry leader who are known worldwide for being one of the best, this could be your chance to join them and contribute to that environment!
Senior CRA â€“ Freelance position â€“ Italy, Spain and Germany
Senior CRA - Freelance position - Italy, Spain and Germany
I am looking for Senior Clinical Research Associates with 5+ years of experience to work Freelance. The company is based in Switzerland, but you will be travelling to sites in Italy, Spain and Germany. Due to the nature of this position, trilingual speakers are most likely to be presented with this opportunity. As a freelancer you can build your CV with an upcoming company and have more time to plan for yourself.
My client is a global pharmaceutical company who are seeking a Director of Pharmacovigilance to join their team in Berkshire. This role involves leading all pharmacovigilance activities within a specified area from phase 1 to 4 and post-marketing. You will be part of a matrix and international cross-functional team. You will ensure continual assesment of Benefit Risk.
A great opportunity has come up to join one of the World's largest pharmaceutical companies as a medical head responsible for oncology and haematology. My client are a global pharmaceutical company who specialise in oncology, and so is an ideal company to join for anyone specialised in oncology.
I am currently looking for an interim medical advisor for a successful global client. This position centers on their diabetes portfolio and is largely a market oriented role, ideal for any diabetes experts who will enjoy a challenging position in an innovative global environment.
Associate Director - Operational Strategy (Early development)
IM/82339/02 Head of Nonclinical Safety - Switzerland My client, a highly respected pharmaceutical company based in the German area of Switzerland are currently looking for a head of preclinical toxicology, based in their global head quarters. This position will give you the chance to be the expert voice working with matrix project teams providing them with advice and guidance, and feed into decisions on the future of compounds in development.
An innovative medical device 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 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.
IM/82339/01 Head of preclinical Toxicology. My client, a highly respected pharmaceutical company based in the German area of Switzerland are currently looking for a head of preclinical toxicology, based in their global head quarters. This position will give you the chance to be the expert voice working with matrix project teams providing them with advice and guidance, and feed into decisions on the future of compounds in development.
Director QA/QC, International manufacturing site role
My client is a successful international biopharma with extensive operations in the Czech Republic. Due to the current director leaving the role they are now looking for a new experienced QA professional to further develop the QA and QC teams. They have an established team in place but will be looking to expand on this in the future.
QA Manager-Medical Devise International Company- Switzerland
My client, a well-known and growing international Medical Devise company, which belongs to one of the most successful pharmaceutical international group, is looking for a Quality Assurance Manager to join their Swiss team. It is a great opportunity to develop your career in a working environment that will allow you to enrich your background, dealing with different sectors and working at the same time independently. ...
All activities related to planning, execution and reporting of clinical trials, development of trial related documents (e.g., protocols, case report forms, data analysis plan, reports), development of presentation material for trial-related advisory boards, investigators meetings, protocol training meetings, on-going review of clinical trial data, final analysis and interpretation of the results. ...
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