CRA’s & CTA’s wanted for UK-wide roles

Following a massive influx of permanent and contract Clinical Research positions, CK Clinical would like all job seeking CRA’s and CTA’s to get in touch.

With jobs that cover all locations in the UK we currently have roles that would suit you at any stage of your career, across all regions. Our clients include independent CRO’s, to global pharmaceuticals and biotechs who are looking for experienced, dedicated professionals with experience across a number of therapy areas, including:

  • Oncology
  • Hepatology
  • Alzheimer’s
  • Diabetes
  • Cardiovascular

If you are interested in finding out more about any of these roles search our jobs here

Or contact our Clinical Research Recruitment Team on:

 

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Interim Head of Clinical Trials Contracts – London

Jim Gleeson is recruiting for an Interim Head of Clinical Trials Contracts for a world renowned health research organisation based in London.

The main responsibilities of this role is to  manage and lead the clinical trials contracts team to support studies that are being carried out by the institute and associated hospital. This will involve managing all contracting agreements with commercial and non-commercial organisations, including drafting, reviewing and negotiating contracts.

This organisations is looking for a professional with a legal qualification and experience managing contracts for clinical trials.

For more information on this role, or to apply, please click here

 

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Early Phase Medical Clinician

Simon Tyson is recruiting for an Early Phase Medical Clinician to work at a new and exciting organisation based in central London.

You will act as a clinical representative for new programme assessment studies, collaborative grant applications and active projects.

A degree in medicine, or an MSc or PhD in life sciences, is needed for this role.

For more information, please click here

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Biopharmaceutical launches data sharing venture

reported by Pharmatimes.com As of the 1st January 2014 the European Federation of Pharmaceutical Industries and Associations’ (EFPIA) and the Pharmaceutical Research Manufacturers of America’s (PhRMA) joint agreement on the sharing of clinical-trial data came into effect.

Under the newly established ‘Principles for Responsible Clinical Trial Data Sharing’, it is now possible for researchers to request access to patient-level data, clinical-trial protocols and clinical-study reports for any new medication approved in the US and the European Union after 1st January 2014.

This new venture highlights the biopharmaceutical sectors commitment to data-sharing as it will dramatically expand the volume of information from clinical trials available to qualified researchers as well as patients and members of the public.

To read more about this new industry principle click here 

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Clinical Trial Regulatory Lead – South East

p>Shreeya Patel at CK Clinical is recruiting a Clinical Trial Regulatory Lead to join a global pharmaceutical company at their site based in the South East on a 6 month contract.

As Clinical Trial Regulatory Lead you will be responsible for managing and assisting in all regulatory aspects for Phase 1 – Phase 4 clinical trial authorization applications conducted globally, regionally or locally, spanning all relevant Therapeutic Areas.

Responsibilities

Main responsibilities will be:

  • Attend/Lead CTA meetings to prepare/compile CTA applications for submission to global Health Authorities.
  • Prepare EudraCT forms.
  • Create/maintain/update CTA content plans.
  • Prepare the list of ongoing trials using available template.
  • Follow-up with Core document owners on status of documents needed for the CTA packages.
  • Interface with publishing/production on publishing/dispatch/submission of CTAs from CTA content plans.
  • Import documents into GRIPS/ERIS for direct filings.
  • Maintain/Update CTA approval status.

 Qualifications

  • Regulatory CTA Experience is essential for this role
  • Previous experience of working with pharmaceutical organisations required.
  • The successful candidate will ideally be educated to degree level

The individual must be proactive and able to work independently requiring minimal supervision

Shreeya Patel - Regulatory Affairs Recruitment Consultant at CK ClinicalHow to apply

Apply online now 

 For more information or to apply for the role, please contact Shreeya Patel on 01438 743047 or email spatel@ckclinical.co.uk. Please quote reference CL25763 in

all correspondence

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