Senior Regulatory Affairs Executive based in Buckinghamshire, UK

Senior Regulatory Affairs Executive required for research and development company based in Buckinghamshire, UK.

Our client, a company which specialises in the research and development of prescription drugs, are currently looking for a Senior Regulatory Affairs Executive to be based in Buckinghamshire.

Reporting to the Regulatory Affairs Manager, your main responsibilities as a Senior Regulatory Affairs Executive will include:

  • Maintenance of clinical trial and marketing authorisation applications.
  • Preparing and submitting applications to the relevant authorities.
  • Keep up to date with legislation’s affecting pharmaceuticals in UK and Europe.
  • Preparation and maintenance of text for PILs, SPCs and more.
  • Take responsibility for ensuring company promotional materials are compliant with legislation’s.
  • Keep in contact and maintain a good working relationship with the MHRA and other regulatory authorities

The ideal candidate for this Senior Regulatory Affairs Executive will have the following skills and competencies:

  • A good work knowledge of regulatory affairs.
  • Excellent written and verbal communication skills.
  • Broad experience in the pharmaceutical industry.
  • Experience within marketing, research and information functions are beneficial.

How to Apply

If you would like to hear more about this Senior Regulatory Affairs Executive role, please contact Meera Pattni on 01438 743047 or email mpattni@ckclinical.co.uk.

Alternatively, click here to apply for this Senior Regulatory Executive job now.

If this vacancy is not exactly what you are looking for why not give us a call, we may be dealing with a vacancy better suited to your needs.

 

About CK Clinical

Finding a new job can be a rather daunting process, at CK Clinical we pride ourselves in our honest and supportive approach. This is the reason why nearly 50% of people we help are referred to us by their colleagues and friends. CK Clinical are preferred suppliers to the top 5 global organisations within our sector aswell as having agreements in place with smaller, more niche organisations too.

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AstraZeneca to cut 1,200 UK jobs

As reported on the Times Online, the Pharmaceutical Industry giant, AstraZeneca plans to cut 1,200 UK Pharmaceutical jobs. The job cuts are a result of the company’s suspension of their research into various disease areas.

The company plans to close its research and development facility based in Leicestershire, along with another small plant in Cambridge.  Pharmaceutical development work at the Avlon facility near Bristol will also cease. Some of the workers will move to the company’s Alderly Park in Cheshire which is AstraZeneca’s largest research and development plant.

This will come as disappointing news to the Government, who created the Office of Life Sciences last year in a bid to increased the number of science and pharmaceutical jobs. The head of the Office of Life Sciences, Lord Drayson, said “I’m obviously disappointed that AstraZeneca is closing Charnwood, but the announcement that Alderley Park will become one of AstraZeneca’s top three global R&D sites shows that the UK remains an attractive location for investment in pharmaceuticals.”

Earlier in the year, AstraZeneca announced that they planned to cut 8,000 jobs around the world by 2014, including 3,500 in research and development, as part of a large-scale refocusing of the business.

Have you been effected by redundancy? Search for pharmaceutical jobs in your area now.

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Immunology Director, Translational Medicine wanted

Immunology Director required for an international pharmaceutical company based in Hertfordshire, UK.

Our client, a leading international pharmaceutical organization, are currently looking for an Immunology Director to join their team based in Hertfordshire, UK. This is a role in which you can make a real difference in the world of drug development.

As Immunology Director, you will play a leadership role in defining strategy across a range of translational medicine projects, working closely with colleagues in discovery and clinical pharmacology. Using your technical expertise in this field you will direct biomarker strategy to support critical decisions for compounds in the early stages of development.

This is very much a cross-functional and cross-departmental position, motivating and mentoring a global team bringing products through to successful registration.

The successful candidate will be a GMC registered medic or a PhD with a strong research (including academic) background, ideally within immunology and have extensive clinical trial leadership experience. Eligibility to work in EU essential.

If you are interested in applying for this Immunology Director role please contact Jim Gleeson on 01438 870027 or email jgleeson@ckclinical.co.uk

Alternatively, click here to apply for this Immunology Director job now.

Not quite what you’re looking for? Click here to search our current pharmaceutical jobs now.

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Director of Translational Medicine in Herts

Our client, a leading international pharmaceutical organization, are currently looking for a Director of Translational Medicine to join their team based in Hertfordshire, UK. This is a role in which you can make a real difference in the world of drug development.

As Director of Translational Medicine, you will play a leadership role in defining strategy across a range of translational medicine projects, working closely with colleagues in discovery and clinical pharmacology. Using your technical expertise in this field you will direct biomarker strategy to support critical decisions for compounds in the early stages of development.

This is very much a cross-functional and cross-departmental position, motivating and mentoring a global team bringing products through to successful registration.

The successful candidate will be a GMC registered medic or a PhD with a strong research (including academic) background, ideally within immunology and have extensive clinical trial leadership experience. Eligibility to work in EU essential.

If you are interested in applying for this Director of Translational Medicine please contact Jim Gleeson on 01438 870027 or email jgleeson@ckclinical.co.uk

Alternatively, click here to apply for this Director of Translational Medicine now.

About CK Clinical

Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry.

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Opinion on Pharmaceutical Industry Job Market 2010

As you may be aware, last year CK Clinical conducted a comparison survey researching the attitudes of jobseekers in the pharmaceutical industry in July 2009 compared to October 2009. We found that respondents generally felt the wider economy was on the mend. However, at grassroots level, employees in the pharmaceutical industry were starting to feel the bite of the recession. You can view an analysis of the survey results here: https://ckclinical.co.uk/news/don%E2%80%99t-panic-it%E2%80%99s-not-all-that-bad/

Now, 4 months on, we are curious to see if attitudes of jobseekers within the industry has changed again. We would really appreciate it if you could take a few minutes to complete my short survey. To complete the survey, please follow this link: http://www.surveymonkey.com/s/ckclinical2010

Once all the responses have been collected, a full analysis will be made available to view on our website.

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Medical Information Advisor job in Luton

Our client, one of the world’s leading pharmaceutical companies, is currently looking for a Medical Information Advisor to join their team based in Luton in Bedfordshire, UK.

Working as a Medical Information Advisor you will provide a high quality, comprehensive, technical and scientific information service for external customers on the product range, supporting and enhancing the safe and effective use of products, enabling customers to make informed decisions about the product range.

Further responsibilities of this Medical Information Advisor role will include:

  • Provide a first line technical and scientific information service to external customers in line with company and industry standards
  • Liaise with the European Medical Information Advisers or Medical Affairs Scientists on enquiries requiring specialist support
  • To be aware of and pass on product and issue focused commercial feedback on products to key internal groups.
  • Ensure Medical Information activities are in line and comply with the ABPI Code of Practice.
  • Responsible for handling all enquiries, in particular adverse event reports and pregnancy reports, in line with local and global procedures and systems.
  • Responsible for the management of Product Quality complaints in line with local and global procedures and systems (GCM) and highlight major quality incidents to the Head of Regulatory Affairs and Medical Information & Patient Safety Manager.
  • Partake in project work as directed by Medical Information & Patient Safety Manager.

The successful applicant for this Medical Information Advisor role will have a Life Sciences Degree and will have experience of working in the pharmaceutical or healthcare industry in a Medical Information role. You will be an effective communicator and be able to work on your own initiative as well as being part of a cross functional team.

This is a fantastic opportunity for the right candidate to develop their career with one of the world’s leading pharmaceutical companies.

If you would like more information about this Medical Information Advisor role, please contact Hendre Moolman on 01438 743 047 or email hmoolman@ckclinical.co.uk.

 

About CK Clinical

Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry.

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CK Clinical to exhibit at the DIA 22nd in Monaco

DIACK Clinical, the leading specialist pharmaceutical industry recruitment agency, is proud to announce that we will be exhibiting at the DIA 22nd Annual EuroMeeting in Monaco on 8-10 March 2010.

If you would like to come along and meet us or enter our competition to win an iPod, our booth number is 212.

If you would like to schedule a private meeting with us at the DIA to discuss your recruitment plans and see how CK Clinical can help, please do contact us on 01438 743 047 or email jhartsmith@ckclinical.co.uk.

Thank you and we hope to see you in Monaco.

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Director Clinical Development job – Greater London

Director of Clinical Development required for global expanding pharmaceutical company based in Greater London.

This is a high profile position in which you will oversee and manage global or regional development programs or multiple multinational phase II/III clinical trials in order to achieve a high quality product for the marketplace and business success for the organisation.

As the Director of Clinical Development you will be the point of contact for interactions with regulatory-agency clinical reviewing divisions on clinical matters, oversee management and performance of CROs and ensure high quality products for the business.

The successful individual must be educated to MD or DPharm level with demonstrable hands on experience leading a multi-country, oncology clinical program.

This is a very rare opportunity to join an expanding global pharmaceutical company and to take your career to the next level.

If you are interested in finding out more about this Director of Clinical Development role please contact Ben Traies at CK Clinical on 01438 743047 or email btraies@ckmedics.com

 

Alternatively, click here to apply for this Director of Clinical Development job now.

Not quite right for you? Click here to search for other pharmaceutical jobs now.

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EU Regulatory Strategist – Regulatory Affairs Jobs

EU Regulatory Strategist required for leading pharmaceutical company based in the South East of England.

Our client, one of the world’s leading pharmaceutical companies is currently looking for an EU Regulatory Strategist to join their team based in the South of England.

Reporting to the EU Regulatory Strategy Portfolio Manager, your role will include:

  • Ensuring EU contribution to Global Regulatory Strategies and implementation plans.
  • Ensuring that the regulatory contributions work towards achieving the objectives in the strategy.
  • Be responsible for providing the required regulatory contributions to project teams, adhering to time and cost deadlines.
  • To liaise with Senior Management regarding regulatory plans.
  • Work closely with the Regulatory Product manager to ensure consistent and appropriate process, working practices and quality standards.

The ideal candidate for this EU Regulatory Strategist role will be educated to a minimum degree level in a scientific subject and will have demonstrable have experience of the following:

  • EU regulations.
  • CTA and MAA submissions process.
  • Management of complex regulatory issues.

If you would like to hear more about this EU Regulatory Strategist job, please contact Meera Pattni on 01438 743047 or email mpattni@ckclinical.co.uk.

Alternatively, click here to apply for this EU Regulatory Strategist job

Not quite what you’re looking for? Click here to search for other pharmaceutical jobs now.

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Clinical Project Manager wanted

Our client is one of the leading world’s leading healthcare companies.  Due to departmental expansion, a new Clinical Project Manager position has arisen. The main focus of this Clinical Project Manager role will be to be responsible for all aspects of allocated clinical trials in Healthcare and / or Personal Care categories.

Working as a Clinical Project Manager, you will provide clinical input to designated projects through the specification of clinical trial requirements and protocols and management of clinical trials. You will work in a multi-functional project teams and will provide clinical input to deliver project requirements, and work with CRO’s, KOL’s and Regulatory bodies to optimise project development strategies.

Further responsibilities of this Clinical Project Manager include:

  • To provide clinical expertise to the design of clinical trials, ensuring trial designs are appropriate to achieve the desired claims and to suggest innovative approaches to achieving the desired endpoints.
  • To ensure that all protocols developed for pharmaceutical clinical trials and cosmetics clinical studies address the business requirements and are fully compliant with all relevant legal and regulatory requirements and SOPs.
  • To ensure that all clinical trials / studies are performed to the required timelines.
  • To ensure that the relevant Clinical Affairs SOPs are implemented for all clinical trials/studies.
  • To be persuasive and influential within the project teams.

The successful candidate for this Clinical Project Manager job will have demonstrable Clinical development experience gained in the pharmaceutical / cosmetic development environment. The ability to work in the EU is a pre-requisite.

This is a fantastic opportunity for the right candidate to develop their career with a fast moving and innovative global healthcare organization.

If you would like to hear more about this Clinical Project Manager vacancy, please contact Jim Gleeson at jgleeson@ckclinical.co.uk or 01438 870027.

Alternatively, apply for this Clinical Project Manager job now.

 

About CK Clinical

Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist recruiters and career consultants are here to help you achieve your career ambitions within the clinical and pharmaceutical industry. We can actively offer you careers advice, help with writing your CV, assistance with your interview preparation and provide you with up to date information about the industry.

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