Our Latest Pharmaceutical Jobs – 10/12/2012

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

Regulatory Affairs

Senior Manager, EU Reg Strategist – Surrey

Regulatory Affairs Specialist – Berkshire

CTRL Coordinator – South East

Senior Manager Regulatory CMC – Middlesex

MEWA Regulatory (Senior) Associate – South East

Regulatory Affairs Manager II – cambridge/Uxbridge

Biometrics:

SAS Programmer -UK

eCRF Developer – London

Principal Programmer – London

Europe:

Clinical Trial Head – Switzerland

Statistics Report Group Manager – Switzerland

HR Business Partner – France

Senior Data Manager – Switzerland

Biostatistician – Switzerland

Global Programme Regulatory Director – Switzerland

Clinical

Clinical Contracts Analyst – West London

AD, Clinical QA &C – London

PV & Drug Safety Recruitment

Clinical Safety Scientist – South East London

Senior Safety Systems Analyst -South East London

 

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 – 26th November 2012

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

Pharmaceutical jobsBiometrics:

Senior Statistical Programmer – Switzerland

Statistical Programmer – Belgium

Data Analyst – Middlesex

Head Of Statistics – UK

Data Analyst – London

Snr/Principal Statistical Programmer – France

Statistician – France

Pharmaceutical jobs - 26th November 2012Senior Statistician Biomarkers – Switzerland

Principal Programmer – Switzerland

Senior Statistician – Switzerland

Senior Statistical Programmer – Switzerland

Regulatory Affairs:

Associate Regulatory GRAAS – Cambridgeshire

Regulatory Affairs Manager III – South East

Senior Medical Writer – Oxfordshire or LondonPharmaceutical Jobs

Science Incubator Marketing, Sales & Event Manager – South East

Associate Regulatory Affairs I – Cambridge

Manager, Document Review And Maintenance – UK/Europe

Medic:

Interim PVG Physician – South East

DrPharmaceutical Jobsug Safety:

Medical Affairs Project Manager – South East

Clinical:

CRA Training Manager – Basel, Switzerland

Departmental Project Leader, R&D QA Switzerland

 

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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Clinical Data Analyst – London

Priya Mukherjee at CK Clinical is currently recruiting for a Clinical Data Analyst to work for a leading pharmaceutical company in the London area.

Responsibilities:

As Clinical Data Analyst, you will have the following responsibilities:

  • Resolving mappings issues picked up through the automated QC reports
  • Reviewing DRAFT mappings developed by others
  • Consulting with the company’s SDTM Committee on mapping related issues
  • Conducting QC of the SDTM datasets to ensure mappings have been implemented correctly
  • Drafting SDTM mappings for NEW core standards
  • Supporting programmers with mapping issues
  • Supporting study teams with outsourced studies

Qualifications, Skills and Experience:

As Clinical Data Analyst you will have the following qualifications, skills and experience:

  • Proven experience of working in Clinical Data Management within the pharmaceutical industry
  • CDISC knowledge in particular SDTM
  • Knowledge and experience of mapping to SDTM standards and knowledge of clinical trial data.

 

Priya Mukherjee - Clinical Data Management Recruitment

Please contact Priya for more details.

How to apply

Click here to apply online now >

For more information regarding this Clinical Data Analyst role, please contact Priya Mukherjee at CK Clinical on +44 (0)207 470 5670 or email pmukherjee@ckclinical.co.uk. Please quote reference CL25704 in all correspondence.

 

 

 

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Click here to search our clinical jobs online now.

 

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Our Latest Pharmaceutical Jobs – 15th November 2012

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

Clinical jobsDrug Safety:

Senior Medical Information Officer – Greater London

Clinical Safety QA Manager – South East

Regulatory Affairs:

Regulatory Affairs Associate  – Mauritius

CK Clinical jobsRegulatory Affairs Leader – Mauritius

Operations Specialist I – Kent

Clinical:

Associate Director, Project Planning – London

Human Resources Administrator – Homecounties

Clinical JobsMedic:

Medical Director – Diabetes/Metabolisim – South East

Biometrics:

SAS Programmer – Welwyn Garden City

 

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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Global Clinical Trials Manager – Hertfordshire

Jim Gleeson at CK Clinical is recruiting for a Global Clinical Trials Manager to join a major pharmaceutical company at their

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site in Hertfordshire on a six month contract.

Responsibilities:

This Global Clinical Trials Manager role is a leadership role overseeing large scale clinical trials from planning to close-out ensuring timelines, budgets and ICH / GCP regulations are fully complied with.

Your responsibilities will include:

  • Development of operational plans covering monitoring strategies, risk mitigation, budgets, site selection and clinical supplies management
  • Leadership of high performing operational teams
  • Development and management of clinical study budgets
  • Leadership of the development of Protocol Feasibility Questionnaires, Site Feasibility Questionnaires and Patient Recruitment Plans
  • Planning and management of the IMP and non-clinical supply chains
  • Proactive management of study level recruitment
  • Management and auditing of third party vendors (CROs, Labs, IVRA etc)
  • Ensuring adherence to ICH / GCP and SOPs

Experience and skills required:

The successful candidate for this Global Clinical Trials Manager will have the following skills and experience:

  • Strong experience of the management of global clinical trials
  • Management of CROs, budgets and IMP supplies
  • Ability to lead global teams
  • Excellent GCP / ICH knowledgeJim Gleeson - Senior Recruiter at CK Clinical

How to apply:

Apply online:

For more information or to apply online for this Global Clinical Trials Manager please contact Jim Gleeson on 01438 743 047 or email jgleeson@ckclinical.co.uk. Please quote reference CL25184 in all correspondence.

 

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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GSK & Cambridge Develop Drugs for Disease

News Medical has reported that a new collaboration between the University of Cambridge and GSK will aim to discover and develop new medicines to treat liver disease.

The collaboration with GSK will combine Professor Lomas’ long-term research at the University of Cambridge Institute for Medical Research (CIMR) with GSK’s expertise in drug discovery and development in order to develop new therapeutics. Work on the project will be carried out both at GSK and at the CIMR.

This new partnership will build upon the work of researchers who have identified a molecular mechanism that plays a major role in the life-threatening liver disease that develops in patients with a particular mutant gene.

Alpha-1 antitrypsin (A1AT) deficiency is one of the most common genetic disorders in the UK, affecting approximately one in 2,000 people. Professor Lomas said that “Currently, the only option for patients with liver disease as a result of alpha-1 antitrypsin deficiency is transplantation…….This partnership brings together our collective expertise in target biology and drug discovery to tackle an unmet medical need and by teaming up with GSK, we have a great opportunity to turn our research into effective treatments”

 

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Medical Science Liaison – South West

Hendre Moolman at CK Clinical is recruiting for a Medical Science Liaison to join a global pharmace

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utical company

in a permanent field based role in the South West.

Responsibilities:

As a Medical Science Liaison the main purpose of your role will be to provide non-promotional scientific and clinical support for the UK business. You will also ensure that all activities and interactions are conducted with regard to all applicable regulations, guidelines, codes of conduct, company policies and accepted standards of best practice.

Further responsibilities of this Medical Science Liaison position will include:

  • Provide scientific and clinical support for, and help maintain professional and credible relationships with, key opinion leaders and academic centres
  • Develop and maintain in-depth knowledge of relevant products, relevant therapeutic areas and the structure and workings of the NHS
  • Deliver credible presentations on scientific matters to physicians, individually or in groups either reactively or proactively
  • Produce and update scientific presentations for assigned therapeutic areas as appropriate
  • Discuss investigator initiated trials and clinical trial details with potential investigators and help co-ordination of clinical investigator meetings
  • Support and present at advisory boards
  • Contribute to the development of brand plans and strategies by providing medical insight and knowledge about the product or disease area
  • Provide field-based support and training to the sales force and other departments as necessary
  • Provide field-based support to assist Medical Information in dealing with enquiries
  • Ensure compliance with all statutory requirements, including the ABPI Prescription Medicines Code of Practice as well as internal processes and procedures for Pharmacovigilance and Regulatory legislation
  • Attend relevant scientific meetings and congresses to keep abreast of new developments and respond to any specific enquiries from healthcare professionals
  • Adhere to the PMCPA Code of Practice for the Pharmaceutical Industry in all aspects of work
  • Comply with statutory requirements and internal processes and procedures for Pharmacovigilance
  • Be cognisant of, and agree to adhere to Company and Medical Directorate SOPs and Guidelines
  • Accountable to Head of Clinical Affairs and indirectly to UK Medical Director.

Qualifications and skills:

As a Medical Science Liaison you will have the following qualifications, skills and experience

  • Life Science degree, preferably PhD, Biochemist, Biologist, Chemist or Pharmacist
  • Experience in the pharmaceutical industry, preferably in a field based liaison role, is desirable.
  • Experience in therapeutic area desirable

Benefits:

As a Medical Science Liaison you will be joining a global pharmaceutical company with the following benefits:

  • You will be working with a global company with a strong pipeline in variety of therapy areas
  • You will have a competitive salary and car allowance
  • Permanent position

HowHendre Moolman - Drug Safety Recruiter at CK Clinical to apply:

Apply online:

For more information or to apply for this Medical Science Liaison position please contact Hendre Moolman on +44 (0)1438 842 970 or email hmoolman@ckclinical.co.uk. Please quote reference CL25188 in all correspondence.

 

Looking for a new job in the pharmaceutical sector? Start by clicking here

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Icon Plc partnership with College Dublin

Pharmatimes have reported that Icon plc have joined a strategic alliance with the University College Dublin to advance research

Icon have said that this new partnership supports a shared vision for transforming research, teaching, training and innovation in the sciences in Ireland and aims to strengthen the ties between academic research and industry.

Icon have established the ICON Newman Fellowship in Genomics as one component of the partnership. This will be a two-year post-doctoral fellowship based at the UCD School of Medicine and Medical Science and at the College’s Complex and Adaptive Systems

Also ICON and the University College Dublin will work collaboratively on ways to enhance drug development.

The partners said that “This programme has “the potential to include tailored teaching programmes and internships in clinical research that will be available in Ireland and internationally through some of UCD’s university partners”,

 

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Alliance Pharma Expands Into Europe

Alliance Pharma have made a positive move into the European market after purchasing three drugs brands from AstraZeneca, reports proactiveinvestors.co.uk.

The drugs, all three of which are anti-malarial, were bought for just over £4 million and will bring Alliance “into new territories and mark [their] first significant steps onto the continent” says Finance Director Richard Wright. Alliance may have to pay a further £1 million dependant on sales of the drugs.

Alliance have also added significant experience in the appointment of new country managers for France and central Europe. Chief Executive John Dawson has said “We are delighted to add these important anti-malarial brands to the Alliance portfolio,” before expressing his delight at the addition of experience to spearhead Alliance’s European expansion.

Looking for a job in the pharmaceutical sector? Start by looking here

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