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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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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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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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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Drug Safety Associate – Buckinghamshire, UK

Drug Safety Associate required for top pharmaceutical company based in Buckinghamshire, UK.

Our client, a top pharmaceutical company, are currently looking for a Drug Safety Associate to join their team based in Buckinghamshire. As a Drug Safety Associate, you will be responsible for the receipt and data entry of adverse event reports following Company Standard Operating Procedures, internal business practices and regulatory guidance documents to ensure compliance with worldwide safety regulations and corporate policies. Previous case processing experience is required.

Further key responsibilities of this Drug Safety Associate role will include:

  • Triage of incoming cases to determine seriousness for prioritisation of daily workflow.
  • Confirmation of Safety Co-ordinator case registry data.
  • Database searches as necessary.
  • Completion of literature searches as necessary.
  • Completion of remaining case data entry, including narrative or auto-narrative.
  • Completion of risk and quality (label, approval, manual coding & quality review steps.
  • Clarification of unclear or illegible information from the LSO or Call Centre.
  • Discuss source documents, coding conventions and ad-hoc queries with Medical Assessment Physician.
  • Completion of protocol request forms as necessary.
  • Preparation of deviation memo as necessary.
  • Request deletions as necessary.
  • Single case unblinding.
  • Understand relevant safety implications regarding contracts with operating companies and/or marketing partners.
  • Review and make suggestions for system and procedure enhancements.
  • Participation in inspections and audits, as required .
  • Participation in local or global project team.

This Drug Safety Associate position will focus on working on an oncology drug, therefore experience in oncology and the Argus database is a desirable. The ideal candidate for this position will also have a Life Science degree or be a qualified nurse.  Pharmacists are not suited unless they have recent experience in Drug Safety.

The successful candidate will enjoy the benefits of working to a global pharmaceutical company, including a competitive rate.

If you would like more information regarding this Drug Safety Associate job, please contact Hendre on Hendre on Tel: +44 (0)1438 870 023 or email hmoolman@ckclinical.co.uk quoting 19282 to indicate your interest.

Apply for this Drug Safety Associate job now.

Not quite what you’re looking for? Click here to search for our other Drug Safety job vacancies now.

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Local Lead Nurse in Oxford

Our client, an established Medical Devices company, are currently looking for a Local Lead Nurse to join their team in Oxford. This is a field based position in which you will be responsible for providing managerial responsibility of home care nursing services following all the policies and procedures in place. You will be responsible for the co-ordination and management of the nursing rota, and recruitment to ensure patient care is of the highest standard.

The main duties of this Local Lead Nurse job include:

  • Co ordination and management of nursing rota.
  • Patient management.
  • Staff training, development, and supervision.
  • Organising staff meetings.
  • Recruitment of home care nurses.
  • Incident management.

The ideal candidate for this Local Lead Nurse job will have:

  • Nursing experience working with critical care patients.
  • Home care/ community experience.
  • Sound knowledge of IV therapy.
  • Team management experience would be preferable.
  • Previous experience of ICU/CCU and paediatric nursing.

If you would like more information about this Local Lead Nurse job contact Meera on Tel: +44 (0)1438 743047 who specialises in this field. Email: mpattni@ckclinical.co.uk.

Apply for this Local Lead Nurse job now.

 

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 oursector as well as having agreements in place with smaller, more niche organisations too.

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CK speaker at the Social Media in Recruitment Conference

social-media-networkTaking place on Thursday 22nd April 2010, the Social Media Recruitment Conference is the second largest of its kind in the UK. CK Clinical, a leading specialist clinical recruitment company, has been recognized by the conference organizers to be a pioneer in the use of social media, and has been invited to speak at the Conference.

Here at CK Clinical, we recognize that there are not enough hours in the day for our specialist clinical Consultants to drive our social media strategy themselves. Therefore, one of the first steps taken was to recruit a Marketing Graduate, Catherine Gutsell, to further develop and promote our online brand and digital communications strategy. The main activities Catherine has engaged in are:

  • Search engine optimization.
  • Using social media such as LinkedIn, Twitter and Facebook to both educate and inform clinical clients and candidates, not just to sell.
  • Using YouTube video job advertisements as a way to connect with candidates in a more human and personalised way.
  • Running regular surveys to gather information about the Clinical and Pharmaceutical industry and communicating findings back through relevant publications and social media.
  • Using online communities such as Ning.com and external blogs to candidates with industry updates and careers advice.

So far, our efforts appear to be working. We have seen a 33% increase in organic hits to our clinical recruitment website. Not only this, but the deployment of our social media strategy has also added value to the experience we provide to both candidates and clients. In terms of our candidates, our use of social media enriches their job seeking experience as it allows us to build long-term sustainable relationships, enabling us to completely understand their needs. From a client’s perspective, by using social media to really get to grips with what the clinical jobseeker is about, we are able to create a great match between candidate and job. This means we do not waste our clients’ time putting inappropriate candidates in front of them.

The aim of the Social Media Recruitment Conference is to help Corporate Recruiters, Recruitment Agencies, Recruitment Advertising Agencies, Job Boards and Recruitment Industry Suppliers get the most from the use of social media. The organizer, Mike Taylor, from Online Recruitment Marketing Specialists, stated, “There were over 150 people at the first Conference which was a clear indication in the interest in Social Media. Next year’s conference will be held some nine months after the first one which means that there will be plenty of new things to talk about and discuss.”

Here at CK Clinical, we are looking forward to sharing our story at the Social Media Recruitment Conference. Speaking of the conference, Catherine stated, “We are honored to be speaking at the Social Media Recruitment Conference and it’s brilliant that our efforts have been noticed by such a prestigious event within the Recruitment Industry. We are really looking forward to sharing our story.”

The conference will take place on Thursday 22nd April 2010 at the British Library Conference Centre in London. If you would like to register to attend Social Media Recruitment Conference, please visit their website.

CK Clinical are a leading clinical recruitment company handling jobs in clinical research and drug development. Our clients include some of the top Pharmaceutical and Biotechnology companies from around the world.

Here at CK Clinical, we pride ourselves on our honest and supportive approach. Our team of specialist clinical recruiters and career consultants are here to help you achieve your career ambitions. 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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