A successful company within the Pharmaceutical Industry currently seeks both entry level and experienced Research Physicians to join their professional team. The successful candidate will ensure the commercial success of the Centre by recruiting patients into clinical trials and ensuring all trials are conducted in compliance with ICH-GCP and local regulations.
A Global Pharma Company (top 20) is looking for a Drug Safety Manager within global drug safety and risk management to join their medical department on a 8 month contract to oversee projects within MEA, Israel and Greece. The ideal candidate would have a high level of experience in a similar position and sound knowledge within Drug Safety. This company is exceptionally interesting & have a highly diverse & innovative pipeline.
Interim Clinical Trial Leader - Munich area - Oncology (m/w)
Interim Clinical Trial Leader - Munich area - Oncology (m/w)Our client is an international organization active in the Pharmaceutical and Life Science sector. They are currently looking for an interim Clinical Trial Leader to join one of their subsidiaries in Munich for 12 months (starting Q4 of 2016) with a possibility of extension depending on the development of the project. ...
Primary Market Research-Assosiate Director-SwissFor those specialists coming from Analytics and Primary Market research background (either agency or Industry) with solid Project Management experience we are offering the opportunity to step into an Assosiate Director level role with a Leading Pharmaceutical company. Feel free to contact me for more details.
Senior Toxicology Manager - pharmaceutical consulting company - Munich - up to 160,000 €
We are currently seeking for a Senior Toxicology Manager who will be responsible for non-clinical safety evaluation throughout the preclinical and development stages for our client’s projects. This is an excellent opportunity to work in a passionate team and contribute to the development of new and well-established companies, while receiving an attractive salary package of up to 160,000 €.
Research Nurse II
Company:Synexus Limited Location: Merseyside Salary: 100,000+ Benefits: Up to UKP 265000.00 per year
Qualified Person (QP) – Durham, 12-month contract - £700–800 p/dayOptimus Life Sciences is working with a global Pharmaceutical Client to find an interim Qualified Person on a 12-month contract. The incumbent will be focusing on the batch-release of sterile products and have experience in Quality Assurance management - (applicants with experience/or knowledge in biological products is a bonus). ...
Senior CMC Regulatory Affairs Manager – Pharmaceutical consulting company - Munich – up to 140,000 €
We are looking for an experienced CMC Regulatory Affairs Manager who wants to use his knowledge in an international operating consulting company with a broad varieties of projects. You can expect an open environment, exciting projects and superb benefits inclusive an opportunity of flexible home-based working.
Senior Director, Clinical Trial Management - America's Fastest Growing Biopharma begins construction of all-new UK based European headquarters
Company:Barrington James Clinical Location: Uxbridge, West Londong, UK (England) Salary: 100,000+ Benefits: Brand new UK based European Headquarters
Closing Date: 21 Oct 16
After securing significant revenue from 3 marketed products America’s fastest growing Biopharm is now pumping their cash in to the launch of their UK and European Clinical Research Operations starting with the grand opening of their European Headquarters to be based in Uxbridge, West London.
Clinical Trial Associate - FreelanceEurope€100.00 Per Hour The opportunityI am currently working with an exciting Immuno-Oncology focused biotech who are looking for an experienced Clinical Trial Associate to work on a freelance contract.The successful candidate will possess the following; * Minimum of 2 years experience in clinical operations. * Must have sound knowledge of ICH-GCP guidelines. * Fluent in English and German is essential. ...
Senior Regulatory Information Management Consultant (Contract)
i-Pharm Consulting are recruiting for…ROLESenior Regulatory Information Management Consultant (Contract Role)LOCATION: West LondonSALARY: £60-£70 per hour ROLE: Leading Biotech are looking for a Senior Regulatory Information Management Consultant to work on an IDMP project. The role will focus on Data Migration from Insight to the new system and also involve project management as well as managing a small team of consultants. ...
Business Development - Food & Beverage - NMR - Home Based
Business Development - Food & Beverage - NMR - Key Account Executive - Home BasedKey Account Executive - Food & Pre-Clinical Science - Business Development - Growing Organisation Currently looking for an experienced Key Account Sales Executive with a strong background working in the Food or Pre-Clinical Industry with a focus dealing with NRM.
Senior Director, Managed Care & Trade
Company:EPM Scientific Location: United States Salary: 100,000+ Benefits: target bonus
Closing Date: 05 Oct 16
$200,000 - $250,000 + target bonusUSA, Must be located near an airportOur client is a global biopharmaceutical company focusing in reproductive health, urology, gastroenterology, endocrinology...
Senior Scientist, Pharmaceutical Sciences & Formulations Needed for Leading Pharmaceutical Company!
My Client is a leading Pharmaceutical business operating globally with a US HQ in the Greater Washington DC area. They are currently looking to secure a Global Project Manager to join a new group within the organisation leading teams both in the US and internationally.
Director or Senior Director of Clinical Trial Management - UK - Oncology
A leading Pharmaceutical company firm has a requirement for;Head of Market InsightPermanent position, Full timeOffice based in SwitzerlandStart Date: Flexible for the right candidateIf you want to discuss about this job you can contact me at firstname.lastname@example.org with your contact number and best availability for a confidential phone conversation.
Associate Director Global Regulatory Affairs – global pharma company – Frankfurt – 120,000 € plus bonus
We are looking for an experienced Regulatory Affairs Manager who wants to use his knowledge about global strategy development in one of the biggest pharmaceutical organizations worldwide. You can expect an open environment, life-changing projects and excellent benefits.
Global Clinical Project Manager - Rare Diseases
Company:TEC Group International Location: Boston, MA - USA Salary: 100,000+ Benefits: 401k, medical, life, PTO, sick pay, bonus
Closing Date: 20 Oct 16
You will be employed by a dynamic, rapidly growing CRO but outsourced entirely to a mid-sized Biotech company based in Cambridge, MA. Your employment contract will be with my CRO client, salary paid by the CRO etc. but you will report directly into the sponsor.
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