Meet Moin Din – Medics Recruitment at CK Clinical

Meet Moin Din, Senior Recruitment Consultant at CK Clinical. Moin specialises in recruiting for Medics and senior level appointments within the Pharmaceutical, CRO, Biotechnology and Healthcare industries.

Moin covers all permanent, interim and contract recruitment within CK Clinical’s Medic Recruitment function. To find out more, please watch Moin’s short video below:

Looking for a Medic job in the Pharmaceutical Industry?

Click here to search our current medic jobs online now.

Alternatively, please call us on +44 (0)1438 743 047 or email info@ckclinical.co.uk.

Click here to meet the rest of the CK Clinical recruitment team.

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Amgen Investment creates 100’s of jobs in Ireland

Recruiter reported that  Amgen are investing £123 million in their site n Ireland, which will create up to 100 new jobs.

The US biotechnology company’s expansion program in Dun Laoghaire will create 100 jobs and also 350 construction jobs in the construction period.

The expansion includes the construction of an 11,700 sq-metre building extension, a new production plant, an expanded warehouse and the major refurbishment of its existing buildings.

Martin VanTrieste, senior vice-president of Quality at Amgen said ““We are very pleased to expand our investment in Ireland…….As we expand internationally, Dun Laoghaire will enhance our global production capability, ensuring continuity of supply of Amgen medicines for seriously ill patients worldwide.

Click here to see our biotechnology roles in the UK and Europe

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Clinical Data Manager Job in London

Priya Mukherjee at CK Clinical is currently recruiting for a Clinical Data Manager to join a leading Pharmaceutical company based in London.

As Clinical Data Manager you will be working in close partnership with Offshore Data Management Staff performing CRF/eCRF data validation to ensure data integrity and quality. You will also manage data queries manual or automated and maintenance of CRF according to data query replies which may involve interpretation and decision making as to appropriate course of action.

Further responsibilities of this Clinical Data Manager job include:

  • To run, review, action and resolve listings of errors/inconsistencies identified by validation checks;
  • T validate and reconcile vendor data as needed; Reconcile the Serious Adverse Events in the CRF/eCRF and Clinical Database with the Central Safety Serious Adverse Events Database;
  • To participate in the QC review of study data prior to study release;
  • To assist with the review and evaluation of protocol against CRF;
  • To report findings to senior staff to assure consistency and accuracy;
  • To assist in the development of data validation specifications;
  • To effectively communicate with colleagues and customers to maintain a consistent approach in handling the work;

The ideal candidate for this Clinical Data Manager job will have a BSc (or equivalent) in a scientific discipline along with proven experience of working as a Data Manager for either a Pharmaceutical, Biotechnology or Clinical Research Organisation. You will also have experience of:

  • EDC Inform
  • Oncology data management
  • Local and central lad validation

 

How to apply:

Click here to apply for this Clinical Data Manager position, or contact Priya Mukherjee at CK Clinical on +44(0)1438 870028 or email pmukherjee@ckclinical.co.uk.  Please quote reference CL23436 in all correspondence.

Click here to search our other Clinical Data Manager jobs now. 

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GSK Breast Cancer Trial Scaled Back

Inpharm.com has reported that GlaxoSmithKline is to scale back a phase III clinical trial looking into potential breast cancer treatments.

The trial, which has been running since 2007, is evaluating the effectiveness of the breast cancer drug Tyverb in four different combinations, following surgery. The patients in the trial receive either Tyverb, Roche’s established drug Herceptin, Herceptin followed by Tyverb or both drugs.

An interim report has indicated that the patients only receiving Tyverb are not demonstrating any improvement compared to Herceptin, so that arm of the trial has been discontinued. Those who are halting their treatment are to discuss other options with trial physicians. 8,400 patients are taking part in the study, and the remaining three trials are to continue as normal.

Looking for a job in the pharmaceutical industry? Start by clicking here, now

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Race Hot’s Up For GSK Investment

The North West Evening Mail has reported the on-going attempts for various towns to attract pharmaceutical company GlaxoSmithKline’s next big investment in the UK.

The half a billion pound investment to build a new biopharmaceutical plant is to be built in one of five places, with the Evening Mail reporting on a site near Ulverston’s attempts to gain the 300 potential jobs. The local council has guaranteed GSK planning permission on an existing plant, and has also dropped the planning fees which could have cost nearly £100,000, as incentives.

Councillor Graham Vincent has voiced his approval of the scheme, believing his council needs to fight for the “incredible” investment potential. The site would be at the cutting edge of the biopharmaceutical industry and set itself apart from traditional chemical manufacturing. However, the council is not being naïve about the race for the investment, determined to do all it can to secure the development which could bring in upwards of £10 million annually for whichever council is chosen. Barnard’s Castle in Durham, as well as plants in Montrose and Irvine in Scotland, are also being considered.

Looking for a job in the pharmaceutical industry? Start by clicking here, now

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ICON and BMS Further Partnership

ICON, already global clinical development partner to Bristol Myers-Squibb, have added to the agreement by announcing a preferred provider agreement with BMS in early-phase studies, reports inpharm.com.

The agreement includes full service clinical pharmacology and exploratory clinical studies, based in Manchester in the UK and elsewhere around the world. ICON will also be responsible for all the scientific support services during the trials, such as biostatistics and clinical monitoring, amongst a variety of others.

Dr Mario Rocci, president of ICON Development Solutions, is looking forward to “demonstrating the same values and efficiencies to BMS’s early phase clinical programmes” as they do with phase II-IV studies. Under this new agreement, ICON expects to be able to report “significant cost savings and productivity” by putting it’s global network to use.

Looking for a job in the pharmaceutical industry? Start by clicking here, now

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GSK Invests in Biotech Start Up

Pharmaceutical company GlaxoSmithKline has given a press release detailing an investment in biotechnology company Autifony Therapeutics Limited.

The £1.25 million investment is to be put into the start up in return for a 25% equity stake, alongside £10 million from other investors including SV Life Sciences. £400,000 is to be put into development data for hearing loss, patent applications and several ion channel modulated compounds.

As part of the agreement, GSK will be eligible to receive another 550,000 shares upon pre-determined milestones being achieved. Upon this, further investment will be made by the consortium of other investors which will reduce GSK’s stake to 13%.

Looking for a job in the pharmaceutical industry? Start by clicking here, now

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EU Approves Proposed Genzyme and Sanofi-Aventis Acquisition

iStock_000006963239Medium[1]As reported by The Wall Street Journal, on Wednesday, the European Union (EU) approved the proposed acquisition of the Biotechnology company Genzyme by French Pharmaceutical company, Sanofi-Aventis.

It was concluded by the EU’s executive arm that the acquisition would not have a negative impact on competition in Europe. They stated, “The Commission’s examination has shown that the proposed transaction would not lead to significant combined market shares in the product categories where the parties’ activities overlap.

“In addition, the proposed transaction also does not raise concerns in the treatment of multiple sclerosis, where both parties are developing treatments. In all cases there will remain a sufficient number of other credible competitors.”

Are you looking for a new position in the EU? Click here to search our current pharmaceutical jobs online now.

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Clinical Manager Job (Respiratory) – Home Counties

  • Permanent
  • Up to £51K

Working for a well known international pharmaceutical company, as Clinical Manager you will use your clinical operations expertise to manage a number of Phase II onwards respiratory studies.

Duties of this Clinical Manager job will include:

  • Ensuring that trials are conducted on time, on budget and to ICH GCP standards.
  • Contribution to protocol design, scientific review of clinical data, reporting and publishing.
  • Management of CROs.
  • Preparation and presentation of training materials.
  • Management of interactions with other functional teams, such as clinical supplies and medical.

 

The ideal candidate for this Clinical Manager job will have the following skills and experience:

  • A relevant BSc, preferably MSc or PhD.
  • Extensive clinical development experience gained in a pharmaceutical or biotechnology company or CRO.
  • A sound scientific understanding of the respiratory disease field.
  • Good knowledge of ICH-GCP requirements.
  • Budgetary experience.

 

Apply Now

For more information or to apply for this Clinical Manager job, please contact Jim Gleeson on Tel: +44 (0) 1438 870027 Email: jgleeson@ckclinical.co.uk.

Alternatively, click here to apply for this Clinical Manager position online now.

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Statistical Programmer – Wales, UK

CK Clinical, the leading independent pharmaceutical recruitment consultancy are recruiting for a Statistical Programmer for a leading CRO based in Wales.


This Statistical Programmer  role will involve taking responsibility for the statistical analysis and reporting of a number of phase I clinical trials, providing input into clinical study protocols, writing statistical analysis plans, performing statistical analyses and reporting of TFLs to internal management and to external clients.

The main responsibilities of this Statistical Programmer role will include:

  • Providing statistical input into the planning and development of clinical study protocols by creating/adapting the appropriate statistical requirements.
  • Being involved in the creation of statistical analysis plans including the designing of data listings, table and figure shells for external clients in liaison with project managers.
  • Providing clinical SAS programming support to projects according to specifications within the statistical analysis plan.

We are interested in applicants that hold an MSc in Statistics with proven experience as a Statistician working for either a Pharmaceutical/CRO/Biotechnology organisation. The ideal candidate for this Statistical Programmer role will also have substantial SAS programming expertise in the BASE, STAT and GRAPH modules of SAS (v9.1.3) to create listings, tables and figures. Working within Phases I & II is also desirable.

Apply Now

For more information, or to apply for this Statistical Programmer online now, please contact Priya at CK Clinical on +44 (0) 1438 870028 or email an updated copy of your CV to: pmukherjee@ckclinical.co.uk.

Alternatively, click here to apply for this Statistical Programmer position online now.

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