Lawrence Harvey are currently partnered on an exclusive basis with an exciting IVD company, seeking a highly qualified Regulatory Affairs specialist to help see them through CE marking on a range of products.
Clinical Project Manager- Basel region – Oncology – 12 months
Company:Amoria Bond Location: Basel-Country Salary: 100,000+
Closing Date: 03 Dec 15
Clinical Project Manager- Basel region – Oncology – 12 monthsWe are currently looking for experience Clinical Project Manager to join one of our international clients at their subsidiary in the Basel region. The client is a fast growing international pharmaceutical company focused on researching, developing and manufacturing medicinal drugs. For their upcoming Project focused on oncology they need a experienced Clinical Project Manager to oversee crucial phases within the trial. ...
A unique and exciting opportunity has arisen for an industry experienced Medic to work for a well-backed start-up Biopharmaceutical Company in their newly established HQ in the UK. This is a fantastic chance to embark on a new challenge and to have strategic input at a key time in this company’s growth.
An internationally known biotechnology company has an opening for a Market Access (Senior Manager) Consultant job at their Berkshire office. The company has a strong reputation for developing innovative therapies for neurological diseases and employs approximately 7,000 people worldwide. This is a 12 month role with the possibility of an extension. ...
We are currently seeking for an experienced Regulatory Affairs Manager who will be responsible for implementing strategic goals and manage a small team of regulatory associates. It is an excellent opportunity to work in a dynamic team and contribute to the development of a well-established company, while receiving an attractive salary package.
Head of Regulatory Affairs Strategy for Biotech start-up
This position will be virtually based in the UK or the US (New Jersey) with the possibility of a West London base late next year as they enter in to Phase 2b. They are looking for individuals who will think creatively as their product is fundamentally transforming and they are blazing new ground. ...
Executive Director, Clinical Development
Company:Skills Alliance Location: South East Salary: 100,000+ Benefits: extensive flexible package
Closing Date: 09 Dec 15
A very rare opportunity to join one of the World`s leading Pharma companies. This is a very senior position within their clinical development team and...
We are currently searching for an experienced program (project manager) to lead the development for a leading biological product. The role will be managing all strategic and operational aspects involved in the drug development cycle working closely with Regulatory, Clinical, R&D and commercial and reports closely to the CEO and the VP for program management.
Senior Program Manager–Alliance Management– Switzerland
An international biotech company developing biosimilars with an excellent pipeline is currently looking for a program manager, who will oversee all projects in the business. This position will have oversight of all internal processes and will deal with external partners and facilitate alliance management for a growing global biotech business.
Senior Regulatory Affairs Manager – leading biomedical technology company – Zurich – up to 180,000 CHF – all EU applicant welcome!
We are currently seeking for an experienced Regulatory Affairs Manager who will be responsible for all regulatory aspects during the development of new VI products. It is an excellent opportunity to work in a dynamic team and contribute to the development of a well-established company, while receiving an attractive salary package.
Global Clinical Project Manager (CPM) – Switzerland – 6+ months
Company:Amoria Bond Location: Switzerland Salary: 100,000+
Closing Date: 01 Dec 15
Global Clinical Project Manager (CPM) – Switzerland – 6+ monthsAmoria Bond is currently looking for a Global Clinical Project Manager based in Switzerland. Our client, an international Pharmaceuticals and Life Science organization, is looking for a Project Manager to oversee one or more clinical operations and to ensure the efficient execution of those operations based on ICH/GCP-standards. ...
Senior Director of Pricing and Market Access - Global Oncology
My client are a global pharmaceutical company that are looking for experienced regulatory affairs professionals to come on board as soon as possible to take part in a variety of product development projects within the medical devices/pharmaceuticals area. This will be an opportunity to come in to a job where you will be engaged from the start to the finish with very innovative devices, such as drug delivery systems. ...
Based in either Germany or the US, this opportunity for an experienced Risk Management professional is ideal for those PV professionals seeking to develop their skill set in a market-leading environment. Alongside an extremely attractive salary and benefits package, my client also provides full relocation assistance for international candidates and the chance to progress in the long-term with one of the Pharmaceutical industry's largest players. ...
Clinical Trial Lead – South-Germany – 12 months+Our client is an international organization active in the Pharmaceutical and Life Science sector. They are currently looking for a Clinical Trial Lead to join one of their subsidiaries in South-Germany for 12 months (starting Q1 of 2016) with a possibility of extension depending on the development of the project. ...
Director of Quality Assurance required for rapidly expanding CRODirector | Quality Assurance | GCP FocusOrland | Florida $110,000 - $150,000 + excellent...
Company:Hydrogen Group Location: Belgium Salary: 100,000+ Benefits: full relocation
Closing Date: 11 Dec 15
A unique opportunity has come up with innovative and successful global pharma company to join a new team developing anti-infective and respiratory compoundsThe main outlines and purpose of the role will be in following areas: * Give input into the Overall Clinical Development Plan in alignment with therapeutic area strategy and compound strategy and documents * Manages cross-functional execution of the overall development plan * Maintains ongoing compound stra
Regulatory Manager-Medical Devices & Pharmaceuticals-SurreyI have a need for a Regulatory professional to join one of my clients on a short term contract. You will have the chance to work on a portfolio that includes both pharma and device product's and will be the sole point of contact for regulatory submissions for an innovative company.
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