Your chance to complete the 2013 CK Clinical Salary Survey is almost over.
The clinical salary survey will be closing at the end of February so this is the last chance you will have to take part. It takes just 5 minutes to complete, and your participation will help us understand what the cialis online 2012 clinical salary brackets were. The results of this survey will be published and will help you with your job and salary expectations for 2013.
Click on the link below to complete the CK Clinical Salary Survey
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industry?
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Thursday, February 14th, 2013
Mylene Paumier is recruiting for a Principal Biostatistician to join a global pharmaceutical company at their site based in Switzerland on a permanent basis.
Responsibilities
As Principal Biostatistician, your responsibilities will include the following:
- Lead the IIS statistical analytic contributions to the clinical development programs within a Franchise, in collaboration with the Statistical Scientist, comprising all relevant technical and disease area knowledge.
- Drive in developing statistical strategic quantitative contributions to regulatory / submission strategy and related documents via expert statistical analytic solutions with excellent interface to the Statistical Scientist: Decision criteria, CSPDs, MAPs, project development strategy and trial designs, responses to HA questions.
- Be responsible for leading statistical analytic solutions for regulatory submissions and health authority interactions, by working with statistical scientists and programmers.
- Provide expert statistical analytic support to the Statistical Scientist in developing the pooling strategy specifically for compounds that are developed for multiple indications within a Franchise and develops the detailed statistical methodology for the MAP, CSPDs and attend submission planning meetings.
- Represent biometrics at the GPT meetings and other internal decisions boards in collaboration with the Statistical Scientist.
- Provide statistical computational expertise for scenarios simulations to optimize program/trial and analysis strategies through to sample size and probability of success calculations in collaboration with the Statistical Scientists for CDP writing.
- Provide expertise specifically to high complexity programs to execute the CSPD, advisory committee tables, figures and listings.
- Ensure high quality for all deliverables and processes.
- Foster efficient expert interfaces with internal and external customers with support of IIS management.
- Drive statistical research in collaboration with statistical scientists and the commercial organization by providing expertise and trouble shooting on computational statistical aspects of the problem.
- Lead the IIS cialis online statistical analytic solutions to the exploratory analyses
e=”padding-top: 25px;”>Qualifications
As Principal Biostatistician, you will have the following qualifications, skills and experience:
- MS (in Statistics or equivalent) with relevant work experience or PhD (in Statistics or equivalent) with relevant work experience
- Proficient knowledge of / experience with SAS/ R/ Splus or any other business or research analytic software
- Proficient in up-to-date statistical knowledge/applications and advance expertise in analytic aspects
- Solid experience in leading statistical analytic support for multiple trials
- Proven knowledge in drug development
- Deep knowledge of data architecture
- Good interpersonal and communication skills
How to apply
Apply online now
For more information or to apply for this Principal Biostatistician position, please contact Mylene Paumier on +44 (0)207 470 5672 or email: mpaumier@ckclinical.co.uk. Please quote reference CL26081 in all correspondence. Entitlement to work in the EEA is essential.
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Click here to view CK Clinicals current Biostatistician vacancies
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Tuesday, January 29th, 2013
As reported by Reuters, speciality pharmaceutical Allergan Inc are locked in a patent battle over their glaucoma drug Lumen.
Fighting against two generic drug makers, they found out on Monday that they had won the first round when the U.S. Court of Appeals for the
Federal
Circuit ruled that it would be an infringement of the patent if they went through with plans to
sell a generic version of Lumigan.
Best known for their anti-wrinkle treatment, Botox, Allergan also has one of the biggest arrays of prescription eye medicines in the industry with Lumigan alone making annual sales of more than $600
million.
Click here to see our latest pharmaceutical jobs
Tags: allergan drug battle, allergan jobs, Allergan news, drug development, drug development jobs, drug pharamcovigilence jobs, Pharmaceutical companies, pharmaceutical jobs
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Wednesday, January 16th, 2013
Hendre Moolman at CK Cinical is recruiting for a PV Systems Specialist to join a company in the pharmaceutical industry in a 12 month fixed term role in the South East.
Responsibilities
As PV Systems Specialist you will be responsible for supporting the Head of PV Systems to maintain validated Pharmacovigilance adverse event systems and provide technical expertise and training to Business Users for current and future PV system use, while acting as an interface between PV and IT and an interface between PV and software vendors.
Further responsibilities of PV Systems Specialist position will include:
- Supporting the Head of PV Systems to manage change control and validation efforts to maintain validated Pharmacovigilance adverse event systems in compliance with Computer Systems Validation Policy and Computer Systems Validation Guidelines
- Providing technical expertise and training to Business Users
- Working with Business Users to compile, validate and run searches of the database
- Assisting Head of PV Systems in troubleshooting issues
- Supporting local, regional and global users as system administrator as required
- Working with Head of PV Systems to continue to develop EEL as the centre of excellence for electronic submissions
- Reviewing and writing of relevant system administrator SOPs and WPs
- Acting as back up to Head of PV Systems
Qualifications
As PV Systems Specialist you will have the following qualifications, skills and experience:
- Science Degree (e.g. pharmacy, Nursing, Life Science)
- Relevant Pharmacovigilance experience
- Extensive experience with adverse event database (ARISg preferred) and electronic (e2b) reporting systems (Cyclone preferred)
- Experience with Reporting Applications such as Business Objects is required
- CSV experience and understanding of Gateway Software, Company & Partner Profiles an advantage
- Strong communications skills – with an ability to communicate technical issues to non- IT specialists<
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- Excellent organisational skills to appropriately priorities workload including multiple projects
Benefits
As PV Systems Specialist you will be joining a global pharmaceutical company based in the South East.
How to apply
Apply online now
For more information or to apply for this PV Systems Specialist position please contact Hendre Moolman on +44 (0)1438 842 970 or email hmoolman@ckclinical.co.uk. Alternatively, please click on the link below to apply online now. Please quote reference CL25882 in all correspondence.
Looking for a job in Pharmacovigilance
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Tuesday, January 15th, 2013
Jim Gleeson at CK Clinical is recruiting for an Epidemiology Research Assistant for a one year contract with a major, global pharmaceutical company based in London.
Responsibilities:
As a Epidemiology Research Assistant you will provide support to a range of epidemiological projects to increase disease understanding related to drug development and clinical trials, such as incidence, risk factors, co-morbidities, phenotypes and biomarkers.
Duties will also involve:
- Conducting literature reviews
- Drafting sections of epidemiological documents
- Management of relevant databases
- Scheduling meetings
- Monitoring budgets and maintaining research agreements with external
experts.
Qualifications:
The successful candidate will have an MSc in Epidemiology and hands-on experience conducting or supporting epidemiological research.
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h=”150″
height=”150″ />How to apply:
Apply online:
For more information or to apply for this Epidemiology Research Assistant role please contact Jim Gleeson on 01438 743 047 or email jgleeson@ckclinical.co.uk. Please quote reference CL25999 in all correspondence.
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Tags: Clinical jobs, clinical jobs uk, clinical roles, Epidemiology jobs, Epidemiology Research Assistant jobs, Epidemiology Research Assistant jobs London, Epidemiology Research assistants London, Epidemiology Research jobs, Epidemiology Research jobs London, Jim Gleeson, pharmaceutical jobs, Pharmaceutical jobs London, pharmaceutical jobs uk, pharmaceutical recruitment, pharmaceutical recruitment agency
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Monday, January 14th, 2013
list – Global Clinical S
upplies” href=”http://ckclinical.co.uk/job/Senior-Specialist-Global-Clinical-Supplies/52796bd1cI3LL”>Senior Specialist – Global Clinical Supplies - Homecounties
Clinical Research Associate - London
CRA, Early Phase, Home-based - North West
Senior Study Management Associate, Urology - Home counties
Clinical Trials Assistant - Homecounties
Cl
inical Research Associate, South West
Biometrics:
SAS Programmer - Hertfordshire
Senior Programmer - North Home Counties
Once registered, one of our specialist Pharmaceutical Recruitment Consultants will be in contact to cheap auto insurance 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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Monday, January 7th, 2013
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 cheapest cialis 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
IMG_5671.jpg”>![]()
=”alignright size-thumbnail wp-image-8647″ title=”Shreeya Patel – Regulatory Affairs Recruitment Consultant at CK Clinical” src=”http://ckclinical.co.uk/wp-content/uploads/2012/07/IMG_5671-150×150.jpg” alt=”Shreeya Patel – Regulatory Affairs Recruitment Consultant at CK Clinical” width=”150″ height=”150″ />How 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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Click here to view our latest Clinical Trial jobs
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Tags: CK Clinical CTA jobs, CK clinical pharmaceutical jobs, Clinical jobs, clinical jobs south east, Clinical trial jobs, clinical trial jobs south, contract clinical job, contract clinical jobs, CTA jobs, CTA jobs south, pharmaceutical jobs, pharmaceutical jobs south
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