Pharmaceutical Jobs of the Week: 18/09/2014

Here are our latest pharmaceutical jobs in this week 18/09/2014:


Medical Information/Affairs, Drug Safety and PV Jobs:

Medical Customer Interface (MCI) Manager – South East

Senior Pharmacovigilance Scientist – Buckinghamshire

Medical Affairs Manager – Epilepsy – Hertfordshire

KAM – Thames Valley  – South East

KAM – South East & South Coast


Regulatory Affairs Jobs:

Senior Manager, CMC, GRA – Hertfordshire

Regulatory Affairs Manager – Middlesex or Cambridge

Manager/Senior Manager, Reg Affairs, Neuro, GRA – Hertfordshire


Clinical Operations/ Physician Jobs:

Associate Director, Clinical Operations – Hertfordshire

Study Site Relations Clinician – Home counties

AD, Clinical Development (Physician) – Cambridgeshire

Feasibility & Patient Recruitment Manager – Middlesex

Regional Medical Monitor – Surrey


Biometrics Jobs:

Senior Programmer – Greater London

SAS Programmer – South East


If these jobs are not right for you, search our other pharmaceutical jobs here



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Regulatory Affairs Manager – Buckinghamshire

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

Responsibilities include managing assigned EU regulatory submissions as well as contributing and advising in the creation of strategic plans for the development of pharmaceuticals.

Our client is looking for a degree qualified Regulatory Affairs professional who has an emphasis on drug development and CTA’s phase 1-3.

For more information or to apply click here


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Regulatory Affairs Manager – Buckinghamshire

Oliver Care is recruiting for a Regulatory Affairs Manager to join a pharmaceutical company a based in the Home Counties, on a permanent basis.

The main responsibilities for this position include managing assigning EU regulatory submissions for a project portfolio spanning early to late phase development. In addition you will need to designing, reviewing and interpreting regulatory guidelines and SOPs in line with current European guidelines.

Our client is looking for an experience Regulatory Affairs professional with a background within oncology.

Click here to apply or for more information on this role



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Join our Regulatory Affairs group on LinkedIn

If you are in Regulatory Affairs and are seeking a new job and careers advice but don’t want to visit multiple resources to access it, the CK Regulatory Affairs Network could be your answer.

With over 600 members across the world, the group lists all our current vacancies as well as provides access to, not only the CK Regulatory Affairs team, but also the skills and experience of the other group members.

Click here to join our Reg Affairs group 



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Head of Regulatory Affairs – London

Oliver is recruiting for a Head of Regulatory Affairs to join a pharmaceutical company at their site in London, on a permanent basis.

Our client is looking for someone who can take full responsibility for all aspects of the Regulatory Affairs and CMC activities in the conduct of early phase clinical trials. This will include preparing and submitting of high quality clinical trial documentation and CTA’s.

This role is available to someone who has significant experience of Regulatory Affairs in the EU/US and effective people management capabilities.

Click here to read the full job description or to apply


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Our Latest Pharmaceutical Jobs – 17/09/2012

Looking for a job in the Pharmaceutical Industry? Please click on the links below to find out about our latest pharmaceutical jobs new in this week:

generic viagra pills

ng-top: 25px;”>Biometrics:

Clinical Project Manager – Switzerland

Pharmacovigilance Officer – Belgium

Expert Clinical Manager – Switzerland

Data Analyst Statistician

Drug Safety:

Medical Information Officer

Medical Development Advisor – South East

Pharmacovigilance & Clinical Trial Administrator

Pharmacovigilance Specialist


Field Based Senior CRA, Oncology

Clinical Support Specialist – North East

Regulatory Affairs:

Regulatory Affairs Leader – Mauritius

Medical Writer/Regulatory Doc Scientist – Hertfordshire

Meeting Planner – Hertfordshire

Associate Director, Reg Affairs, CMC


Medical Affairs Manager – Oncology – South East


Register your CV with CK Clinical

Not quite what you’re looking for? Click here to register your CV with CK Clinical today.

Once registered, one of our specialist Pharmaceutical Recruitment Consultants will be in contact to discuss your requirements and any relevant pharmaceutical jobs we are recruiting for at the moment. Good luck with your job hunt

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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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Regulatory Affairs Manager II – London

Priya Mukherjee at CK Clinical is currently recruiting for a contract Regulatory Affairs, Emerging Markets Manager to work for a leading organisation in London.

The job:

As a Regulatory Affairs Manager II you will use expertise in emerging markets to provide input into product strategy for the region, preparing International Market Applications for new products, reviewing post-marketing variations and leading the preparation of responses to agency questions.

Key Responsibilities:

The key responsibilities of this Regulatory Affairs Manager II role are:

• Manage execution of product strategies for assigned MAA and variations.

• Interface with regional regulatory, EM commercial and Operation to develop specific strategies for activities that impact the EM region.

• Keep abreast of changes in legislation and understand the impact on current and future submissions.

• Execute successful marketing application within region

• Liaise with CMC and support the execution of labelling variations in region

• Reports status of assigned registration and life cycle management activities and projects to EM product Lead

• Provide guidance on regional regulatory mechanisms to optimize product registration

• Work with Emerging Markets Product Lead to assess the impact of variations across EM region

• Actively contribute to product strategy for assigned markets

• Track status Marketing Authorizations Applications and Variations submissions and approvals.

• Advocate and actively support regulatory and safety compliance for products supplied across EM

• Troubleshoot and resolve any problems on the critical path to registrations in concert with the key stakeholders

• Lead the preparation and respond to questions raised by authorities within region

Qualifications and skills:

Interested applicant for this Regulatory Affairs Manager II role should hold:

• Bachelors degree, OR equivalent combination of education and experience

• Significant proven regulatory experience

• Strong knowledge and experience within Emerging Markets

• Ability to work within a dynamic matrix environment

• Strong proven leadership skills, with the ability to take responsibility, make informed decisions and direct the activity of others in matrix, internal or external reporting relationships

• The ability to work with policies, procedures and SOP’s

• Proven experience with national legislation and regulations relating to medicinal products

• An understanding of the registration procedures in the EM region for MA, post approval changes, Line extensions and renewals for Medicinal products.

• An understanding of drug development

How to apply:

Apply online now:

For more information or to apply for this Regulatory Affairs Manager II role please contact Priya Mukherjee on +44 (0)1438 743047 or email

Are you looking for a new role in regulatory affairs? Click here to see our latest regulatory affairs jobs

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Meet Meera Pattni – Specialist Regulatory Affairs Consultant

Meet Meera Pattni, specialist Regulatory Affairs Consultant at CK Clinical.

If you are looking for a new position in Regulatory Affairs or are looking to expand your team, please contact Meera today!

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Regulatory Affairs Executive – Southampton, UK

As a Regulatory Affairs Executive you will assist in regulatory activities relating to the UK and Irish division, ensuring compliance of all medicinal products.

Your main responsibilities will include:

  • Ensure compliance of medicinal products to UK, IMB and EU legislations.
  • Facilitate the process of submissions relating to MAA in the UK and Ireland and coordinate the submission and responses as appropriate for European procedures.
  • Provide expert advice to other departments in relation to UK and Irish regulations.
  • Provide input and coordinate product package and final artwork.
  • Ensure compliance with internal and external SOPs.
  • Ensure all paper and electronic documents are correctly filed.

The ideal candidate for this Regulatory Affairs Executive position will have the following experience and skills:

  • Previous experience within regulatory affairs in the pharmaceutical industry essential.
  • Post marketing maintenance experience essential.
  • Experience liaising with the MHRA and IMB required.
  • Excellent attention to detail.
  • Excellent written and verbal communication.
  • Computer literate.


 Apply Now

For more information, or to apply for this Regulatory Affairs Executive position, please contact Meera on 01438 743 047 or email

Alternatively, click here to apply for this Regulatory Affairs Executive role online now.

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