Medical Device Expert – East Midlands

CK Clinical is recruiting for a Medical Device Expert to join one of the largest health care manufacturers in Europe at their site based in the East Midlands.

The overall purpose of this role will be to provide expert regulatory leadership for medical devices,  define technical and regulatory strategies for medical device product development projects.

To be considered for this role you will need to be educated to degree level or above in a scientific field with significant experience in medical device product development and gaining regulatory approval as a device manufacturer.

This is an exciting role with the medical device industry offering a very competitive salary and benefits.


Find out more about this job here



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Regulatory Program Manager Job -Hertfordshire/Basel

CK Clinical is searching for a Regulatory Program Manager in Oncology to join a leading pharmaceutical organisation at their site based in Hertfordshire or Basel on a permanent basis.

This is an excellent opportunity to join a company at the forefront of ground-breaking new medicines, consistently pushing the boundaries of conventional thinking and embracing innovation.

In order to be considered for this role the ideal candidate must have experience within the oncology and haematology therapeutic areas as well as a good understanding of drug discovery and development.


Find out more about this job here




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Regulatory CMC Specialist Job

A  world leader in generic pharmaceuticals is recruiting for a Regulatory CMC Specialist to join them at their site in the South East on a permanent basis.

The main purpose of the role will be to formulate and lead local CMC regulatory strategy for marketed products, maximising the business benefit balanced with regulatory compliance.

To be considered for this role you will need to have knowledge and experience of regulations, MHRA/EMA/ICH guidelines, product lifecycle maintenance and experience in the drug development process is desired.


Find out more about this job here


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Clinical Jobs of the Week: 26/06/2014

Here our latest clinical jobs in this week 26/06/2014:



Clinical Development Scientist – Middlesex

Clinical Study Manager – Surrey

Clinical Operations Expert Support – Basel


Regulatory Affairs:

Principle Regulatory Officer – Home counties

Program Leader – South West London



Global Data Manager – Belgium

Principal Programmer – London

Clinical Data Manager – London

Clinical Programmer – South East


PV & Medical Affairs:

Medical Information Manager – South East

Medical Science Liaison (Mat Cover) – Home & field based

Safety Surveillance Associate – Kent

Pharmacovigilance Officer – Middlesex


Market Access/Clinical Supplies

Strategic Pricing Specialist, Field Based

Clinical Supplies Senior Planner, West London



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CK Clinical launches new mobile website

CK Clinical has launched a dynamic new mobile website which provides the ultimate job-hunting-on-the-move experience. With functionality that enables users to search for jobs through their mobile devices, watch our best videos and find the right consultant for you.

Registered CK+ members are even able to log in and apply for jobs through the interactive new mobile site.

So make sure you sign up for CK+ today.

The new CK Clinical mobile website offers a great user experience for everyone. Keep your eyes open for further developments on our CK Clinical website.

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The KPMG/REC latest report on jobs released

The latest KPMG/REC Report on Jobs has been released and it makes very positive reading for the clinical science sectors. The pace of growth of permanent vacancies has continued with the increase nearly back to the same number as February’s record figures. The rise in temporary vacancies within the clinical field also has been dramatic, and while not as strong as the permanent side, there is still continued growth. The increased demand for permanent  staff  is a sign of the growing confidence employers have in the current market as are investing heavily in additional resources.

The report reflects what CK Clinical are seeing in the day to day job market with the decline in candidate availability and the fastest growth in permanent salaries since July 2007. As a consequence we are starting to see permanent salaries for clinical specialists rising above inflation rates for the first time in over 5 years. This is what we have needed in the clinical field to help attract new talent into the industry whilst retaining the highly skilled specialists in this field.

The clinical sector is among the fastest growing sectors in the economy, slightly behind science and engineering which is great news for our industry.

If you would like more information on this report or the current labour market contact Liam O Connell at

Or click here to search our jobs


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Regulatory Affairs Manager – Home Counties

Oliver Care is recruiting for a Regulatory Affairs Manager to join a leading pharmaceutical company at their site in the Home Counties on a permanent basis.

Responsibilities include managing assigned EU regulatory submissions to obtain approval of CTAs and MAAs for a project portfolio which covers early to late phase development. You will also need to support the development of strategies and provide guidance in the development of pharmaceuticals through advising on submissions, evaluating the content and preparing regulatory documents for submission when required.

Our client is looking for a Regulatory Affairs professional with an emphasis on drug development and CTA’s phase 1-3, and experience within the oncology therapeutic area.

Click here for more information or to apply


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CK Group a top SME in Derbyshire

CK Group is one of North Derbyshire’s top 50 SME’s according to research undertaken by Barber Harrison & Platt (BHP), a local chartered accountants. Contributing to an annual turnover of £633 million and the employment of nearly 4300 people, CK Group is proud to have become a central part of the economic growth of the region.

With three regional offices across the UK, CK Group are the owners of three recruitment brands – CK Science, CK Clinical and CK IT which specialise in the recruitment of scientific, pharmaceutical and technical roles across the UK and Europe.

CK Group has big plans in place for 2014, including responding to global recruitment demands, establishing our position as a leader in workforce outsourcing solutions and launching a new, dedicated Engineering division.

For more information on CK Group click here

If you would like to discuss your recruitment with one of our dedicated consultants, click here



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Emerging Markets Pharmaceutical Regulatory Affairs Job in South East UK

Shreeya Patel at CK Clinical is currently looking for an Emerging Markets Regulatory Affairs professional to join a global pharmaceutical company at their site based in the South East UK. This Pharmaceutical Regulatory Affairs position is a contract position.


About this Regulatory Affairs Contract Role:

As an Emerging Markets Pharmaceutical Regulatory Affairs contractor you will create the CMC sections of Emerging Market initial submissions for established and/or new products and pass to the Product Strategist by the required date.

You will also respond to CMC-related questions as part of the project team, by the required date and to use established systems (particularly web-based document management systems) to ensure global transparency of submitted and approved documentation.

Qualifications, Skills and Experience:

To be considered for this Regulatory Affairs position, you will have the following qualifications, skills and experience:

  • Demonstrable Regulatory Affairs experience in European and/or global market primary applications
  • A broad understanding of European legislation and both technical and procedural guidance; ICH CTD; applicable Module 3 guidance; and variations legislation and guidance at a European and/or global level.
  • Good IT skills including use of Documentum based document management systems.
  • You will be a team player, with strong communication and negotiation skills
  • You will have the ability to work independently and to build strategic working relationships

How to apply:

Shreeya Patel - Pharmaceutical Regulatory Affairs Recruitment at CK Clinical

Please contact Shreeya for more details.

Click here to apply online now.

For more information regarding this Pharmaceutical Reg Affairs contract position, please contact Shreeya Patel at CK Clinical on +44 (0)1438 743 047 or email Please quote reference CL24497 in all correspondence.

Not quite what you’re looking for?

Click here to search our current Pharmaceutical Regulatory Affairs vacancies online now.

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CK Clinical welcomes 2 new Recruitment Consultants!

CK Clinical Expand their Biometrics and Regulatory Affairs Recruitment Teams

Due to our great success recruiting for the Pharmaceutical and Biotechnology industries, here at CK Clinical we have expanded our Biometrics and Regulatory Affairs recruitment teams with the appointment of two new Recruitment Consultants – Mylene Paumier and Shreeya Patel.

Meet Mylene – Biometrics Recruitment at CK Clinical

Mylene Paumier - Biometrics Recruitment at CK ClinicalWe are very excited to welcome Mylene Paumier to the CK Clinical Team. Mylene has joined us as  a Recruitment Consultant and will be working along side Priya Mukherjee, specialising in Biometrics recruitment.

Mylene completed her studies in International Business in France at Rouen Business School, during which she spent one year in Japan at Ritsumeikan Asia Pacific University as exchange student. Following this, Mylene completed her Master 2 in International Business at Aston University in the UK.

During her studies, Mylene worked as a recruiter at ExxonMobil as a recruiter for almost one year and focused on recruiting in engineering and business people across France and Europe. After completing her Master 2, Mylene joined Michael Page for 6 months before joining CK Clinical.

Mylene’s big passion is travelling the world, and also enjoying going to the gym, aerobics and fitness.

Meet Shreeya Patel – Regulatory Affairs Recruitment at CK Clinical

Shreeya Patel - Pharmaceutical Regulatory Affairs Recruitment at CK ClinicalWe are also extremely excited to welcome Shreeya to the CK Clinical team. Shreeya has joined us as a Recruitment Consultant specialising in Regulatory Affairs.

Shreeya is a graduate from the University of Manchester where she studied Business Management and German (and loved every minute of it!). Following university, Shreeya worked for a high street recruitment consultancy for 8 months.

In her spare time, Shreeya enjoys socialising with her friends and travelling around the country visiting her friends from University. She also is a big fan of shopping, hitting the gym and watching television.

The team here at CK Clinical wish Mylene and Shreeya a very warm welcome to our team and wish them every success if their new recruitment roles.

Meet the CK Clinical Recruitment TeamClick here to meet the CK Clinical team >



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