Pharmaceutical Jobs of the Week: 25/09/2014

Here are our latest pharmaceutical jobs of the week 25/09/2014:

 

Sales and Marketing Jobs:

Hospital Sales Specialist – Central London

Hospital Sales Specialist – Scotland

Hospital Sales Specialist – North London

 

Finance Jobs:

Financial Analyst EMEA

 

Clinical Operations Jobs:

Clinical Study Manager – Cambridge or Middlesex

Clinical Research Nurse – North West

Associate Director, Clinical Operations – Hertfordshire

 

Market Access/Health Economics Jobs:

Market Access Manager – London

Health Economics Manager – South East

 

Biometrics Jobs:

Principal Biostatistician – Home counties

 

Regulatory Affairs Jobs:

UK Clinical Trial Regulatory Leader – South East

Senior Manager, CMC, GRA – Hertfordshire

 

Med Info Jobs:

Scientific Review & Info Specialist – South East

Medical Customer Interface (MCI) Manager – South East

Senior Pharmacovigilance Scientist – Buckinghamshire

 

If this is not quite what you are looking for, search our other pharmaceutical jobs here

 

 

 

 

 

 

 

 

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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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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:

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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

Clinical:

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

Medic:

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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Our Latest Pharmaceutical Jobs – 25.6.2012

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:

New pharmaceutical roles in the UK and Europe:

Director, CMC, Regulatory Affairs

Documentation Specialist in Switzerland

Clinical Safety Scientist – Contract

Biomedical Data Statistician in Swavesey

Technical Regulatory Officer in Switzerland

Clinical Data Manager

Hub Labeling Manager in Surrey

Medical Director – CNS

Clinical Study Specialist

Senior Analyst – Regulatory Compliance

Snr Medical Advisor – Haematology

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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Our Latest Pharmaceutical Jobs – 19.6.2012

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:

Clinical:

Clinical Study Manager

Medical Information Manager

Clinical Operations Manager, Oncology

Biometrics:

Senior Business Analyst – Germany

Contract Statistical Programmer

Contract Biostatistician

Regulatory Affairs Jobs:

Senior Manager, Regulatory Affairs, CMC

Pharmaceutical:

Pharmacovigilance Standards Officer

PV Project Manager

Pharmacovigilance Manager

Senior Director, Human Resources

Senior Pharmacovigilance Scientist

Senior Director, Finance

Associate Director of PV

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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Senior Regulatory Affairs Manager – Nephrology and Inflammation, based in Cambridge and Uxbridge, UK

Our client, a leading biotechnology company, is currently looking for an experienced Senior Regulatory Affairs Manager to join their Nephrology and Inflammation Therapeutic Area.

As a Senior Regulatory Affairs manager, your role will be to develop and implement regulatory strategies to expedite global drug development and registration and to manage the execution of regional strategies and regulatory communications and submissions. You will assist in providing expertise on regional regulatory requirements and precedence to interdepartmental teams.

Further key activities of this Senior Regulatory Affairs Manager job will include:

  • Participate through the Global Regulatory Team in the development of product label and core data sheet.
  • Respond to requests from the Global development team and functional areas.
  • Advocate and actively support regulatory compliance.
  • Help to develop regional regulatory strategy for integration into the Global Regulatory Plan.
  • Develop TA expertise.
  • Help resolve any problems on the critical path to regional registration in concert with global registration strategy.

The ideal candidate for this Senior Regulatory Affairs Manager job will be qualified to a minimum Bachelors degree. You will have in-depth experience of Regulatory Affairs Research Development or related area in the Biotech/Pharmaceutical industry, along with experience in inflammation, drug development and CMC knowledge. Line management experience is also desirable.

How to Apply

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

Alternatively, click here to apply for this Senior Regulatory Affairs Manager 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 our sector as well as having agreements in place with smaller, more niche organisations too.

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Associate Director CMC Project Management based in Cambridgeshire, UK

Our client, a global biotechnology group, are currently looking for an Associate Director CMC Project Management to join their team based in Cambridgeshire. Your remit will be to lead CMC Project Teams and provide strategic input for product development whilst ensuring that projects proceed to budgetary, timeline and quality standards. Key responsibilities or this Associate Director role will be:

–          To lead CMC Project Teams, coordinating globally across the company and with external organisations

–          Identify project risks and manage the production of action plans to resolve these issues

–          Promote the interaction of cross-functional teams to ensure efficient transfer of information and material

–          Ensure that all project documentation is produced and maintained in support of the Product Development Plan.

The successful candidate will be educated to BSc (preferably PhD) in a relevant technical subject. Extensive experience of the cross-functional CMC aspects of biopharmaceutical product development is also essential. This Associate Director position also requires a candidate with strong organisational and managerial skills, as well as deep technical understanding, strategic vision and good organisational acumen.

If you would like further details please contact Jim Gleeson on 01438 870027  or email jgleeson@ckclinical.co.uk. Alternatively, to apply, please click here.

 

About CK Clinical

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 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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Scientific Writer – Cambridge, South East, UK

A Scientific Writer job has arisen at a leading Biologics Research and Development company in Cambridge. Our client is committed to developing better medicines that help people live healthier, longer, and more satisfying lives. This innovative company is focused on the areas of infection, respiratory and inflammatory disease, oncology and neuroscience. With a strong current and future product portfolio, both the company and the team are rapidly expanding. With excellent staff retention, their state-of- the-art Cambridge site is home to around 400 employees, and serves the company’s European hub for research and development.

CK Clinical are currently helping this prestigious company to recruit a Scientific Writer on a permanent basis within their Project Management and Business Operations group in Cambridge.

As a Scientific Writer, you will have considerable experience in the biopharmaceutical industry, preferably in the biologics area. With a background in Regulatory Affairs, your experience will include direct experience in preparing CMC regulatory documents for early phase clinical studies. You will demonstrate a good knowledge of the drug development process including an understanding of the relevant technical areas involved. Strong communication skills are essential as you will be interfacing across the business at all levels.

Educated to at least degree level, you will play a pivotal role in helping this pioneering company achieve their ambitions. Our client is looking for a proactive team player with a meticulous, logical and analytical approach to problem solving, good interpersonal skills and a passion for personal development.

With an excellent benefits package, this Scientific Writer position will provide you with the opportunity to work within a team at the core of the business, providing you with plenty of scope for you to make your mark and develop your career. This is a great chance for you to further your personal and professional development. Although this Scientific Writer job is traditionally an office based role, the company does allow flexible working hours.

If you believe you are the right person for this job, please contact Jonathan Hart-Smith on 0845 034 3082, or email jhartsmith@ckclinical.co.uk. Alternatively, to apply, click here.

You may wish to meet some of our consultants and hear more about our current vacancies, if so, please visit our Youtube Channel.

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. 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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