Blue Pelican are a specialist recruitment business passionate about offering an exceptional level of service to candidates and clients alike. We pride ourselves on being honest, ethical, professional, knowledgeable Recruitment Experts, with Consultants who are genuine specialists in their fields. These are the principles we are known for and our aim is to set the standard for recruitment excellence.
Blue Pelican specialise within four specialist functions - Legal, Marketing, Pharmaceutical and Technology.
Take responsibility for coordinating and managing local and regional market access business in the UK Review local market access value propositions, making sure that the highest standard is maintained in an effective manner. Co-ordinate and take the lead in various company, market access meetings Ensure the best outcome for all the clients brands Be responsible for local and regional payer materials using information based...
Regulatory Affairs Manager It’s a terrifically exciting time to be working at this global pharmaceutical company. Would you like to do a regulatory affairs role where you really get to work at a Global level? This role offers exceptional, above average financial benefits Do you have the following experience? • A university Degree in a Scientific discipline. • At least 5 years or more of regulatory...
Regulatory Affairs Officer My client is one of the most respected companies in their field. They have an exceptional track record and have one of the most dynamic and impressive regulatory Affairs teams in the UK Do you want to work in a super company that truly values its regulatory professionals? Do you have the following experience? • 1-2 years of pharmaceutical regulatory affairs experience. • Knowledge ...
Senior Regulatory Affairs Officer My client is one of the most respected companies in their field. They have an exceptional track record and have one of the most dynamic and impressive regulatory Affairs teams in the UK Do you want to work in a super company that truly values its regulatory professionals? Do you have the following experience? • 3 years or more of pharmaceutical regulatory affairs experience.<br /...
Research Nurse/Senior Research Nurse Category: Pharmaceutical/Science & Research Type: Permanent Location: Manchester Salary: £25,000-£27,000 Are you a registered nurse looking for a new and exciting opportunity? Are you interested in working in clinical trials? My client is a fast growing clinical research organization. They have just opened a new office in Manchester and are lo...
Research Assistant/Research Scientist Category: Pharmaceutical/Science & Research Type: Fixed Term Contract- Finishing Dec ‘13 Location: Cambridge Salary: £21,000-£35,000 Are you a competent life science professional with good lab experience looking for a step into the pharmaceutical industry? Do you have experience performing commonly used techniques? Our client is looking for e...
Lead Clinical Support Specialist Category: Pharmaceutical/Science & Research Type: Fixed Term Contract with a view to a permanent role Location: Cambridge Salary: £25,000 Do you have experience working in a clinical trials setting? Have you managed, trained or mentored junior members of staff? My client is a rapidly growing CRO who have expanding offices in Cambridge. They are looking...
Senior Clinical Project Manager Category: Pharmaceutical/Science & Research Type: Permanent Location: Southern UK Salary: £51,000+ Car and Benefits Do you have a strong background in clinical research with a good knowledge of the drug development process? Have you worked in a clinical project management capacity in the life science industry? We’re working with one of the world’s b...
This role of QA advisor is working for a rapidly expanding Clinical Research Organisation (CRO) within a highly specialised field. A large part of your role as advisor will be to audit the GCP activities within the business and identify areas which are ineffective and implement changes to the quality systems. Your key responsibilities will be conducting internal and external audits, hosting audits and keeping the quality management ...
I have a role for a QA Scientist working for an innovative, growing and specialist pharmaceutical organisation based in Surrey. You will have responsibility for deputising for the Responsible Person, review of clinical and batch records as well as the documentation management system. This role is a wonderful opportunity to work within in a progressive and innovative organisation who actively encourage progression. The company is an ...
Clinical Trial Medical Review Specialist Category: Pharmaceutical/Science & Research Type: Fixed Term Contract- Part Time 17.5 hours per week Location: Southern UK Salary: £35 per hour Do you have a strong background in clinical research with a good knowledge of drug development process? We’re working with one of the world’s best specialist pharma companies who are recruiting for a Clinica...
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Date: 16 May
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Italy,
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Salary negotiable
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3 applications
My client is looking for a Senior Regulatory Affairs Group Manager to be based in Italy. Candidates with strong biologics and development experience would be very well suited to this position. This company is highly respected and you will be part of their international team. They will provide relocation assistance. The ideal person will have the following experience. • Up to 10 years pharmaceutical regulatory affairs e...
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Date: 16 May
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Italy,
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Salary negotiable
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2 applications
My client is looking for a Regulatory Affairs CMC Manager to be based in Italy. If you have a Biologics background they would be particularly keen to speak with you. This is an excellent global pharmaceutical company with huge potential career growth. They are developing exciting medicine and you will be able to work at an international level. RELOCATION COSTS AVAILABLE Do you have the following experience and intere...
Clinical Trial Patient Recruitment Project Manager Category: Pharmaceutical/Science & Research Type: Permanent Location: Southern UK Salary: £53,000+ Car and Benefits Do you have a strong background in clinical research with a good knowledge of drug development process? Have you worked in a project management capacity with budget management responsibilities? Do you have experience build...
This role of Senior QA Manager is working for a rapidly expanding Clinical Research Organisation (CRO) within a highly specialised field. This role is working as overall Manager of Quality Assurance to ensure all the quality standards are met and adhered and raise Quality awareness through all departments throughout this exciting period of expansion. This organisation has grown by doubling headcount and expanding geographically thro...
