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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Clinical Jobs of the Week: 14/08/2014

Here are our latest jobs in this week: 14/08/2014

 

Clinical Operations Jobs:

Clinical Research Nurse – Salford

Clinical Operations Manager – London

Associate Manager, Clinical Outsourcing – Hertfordshire

 

Statistics Jobs:

Global Data Manager – Belgium

Senior Manager – Statistical Programming – South East UK

Clinical Data Manager – London

 

PV & Medical Affairs Jobs:

Senior Product Manager – Immunology – Middlesex

Senior Product Manager – Oncology – Middlesex

Senior Medical Advisor, Pain – Cambridge

 

Regulatory Affairs Jobs:

Senior Associate GRAAS Regulatory Operations – Cambridge

Medical Affairs Advisor – London

Artwork Project Manager – South East

 

 

 Search our other jobs here

 

 

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Click here to see, Jobs of the week 31/07/14

Here are CK Clinical’s job of the week for 31/07/14!

Biometrics

Senior Clinical Programmer – South East

 

Medical/QA jobs

Interim Head, Clinical Trials – London

Early Phase Medical Clinician – London

Clinical Development Scientist – South East

 

Clinical Operations

Global Studies Manager – South East

Manager, Clinical Outsourcing – South East

Administrative Coordinator – South East

 

Regulatory Affairs

Regulatory Affairs Officer – South East

 

PV/Med Affairs

Key Account Manager – South East

Medical Science Liaison – Midlands

Medical Science Liaison – Ireland

Drug Safety Advisor – South East

Medical Science Liaison – Northern UK

 

For a more comprehensive job search, click here!

 

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Regulatory Affairs Manager – London

Oliver Care is recruiting for a Regulatory Affairs Manager to join a cell therapy company based in London on a permanent basis.

The main responsibilities in this role include implementing optimal regulatory strategies in agreement with the Head of RA, COO and key stakeholders as well as compiling and submitting all regulatory submissions ensuring they meet agreed time, cost and quality standards.

Our client is looking for the ideal candidate to have proven experience in delivering high quality regulatory documents and knowledge of advanced therapy/cell based medicinal products.

Click here to find out more about this position or to apply

 

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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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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 – 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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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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Clinical jobs of the week: 07/04/2014

Here are our latest clinical jobs in this week 07/04/2014:

 

Biometrics:

Biostatistician – Switzerland

 

Sales, Marketing & Market Access:

Reimbursement and Access Manager – North East

Hospital Sales Specialist – Midlands (Epilepsy)

 

PV & Medical Affairs/Information:

Pharmacovigilance Manager – Fixed Term – Hertfordshire

 

Regulatory Affairs:

Regulatory Affairs Manager CMC – London

Regulatory Affairs Team Leader  – London

Regulatory Portfolio Project Manager – South East

Artwork Project Manager – South East

 

Clinical Operations:

AD Clinical Operations, Oncology – Home counties

Regulatory Scientist – South East

 

 

 

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Regulatory Executive – Middlesex

Oliver Care is recruiting for a Regulatory Executive to join a pharmaceutical company at their site in Middlesex on a contract basis.

Responsibilities for this role include developing and maintaining the Global Product Information for prescribing, patient and packaging information. You will also be required to support regional and country product information primarily in EU and APJEM markets.

The ideal candidate is required to have a life science degree or PhD with relevant experience and the ability to produce written regulatory scientific communications with clarity and accuracy.

For more information or to apply click here >

 

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