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Optimus Life Sciences have open roles for permanent and freelance workers with skills in Programming and Statistics. If you could be tempted by a change, click the links below to find out more about some live jobs that we could offer! Homebased Permanent Statistician (UK): http://oslifesciences.com/vacancies/senior-statistician-2/Site-based Permanent Statistician (Belgium): http://oslifesciences.com/vacancies/non-clinical-statistician-belgium-e60000/Site-based Freelance Biostatistician (Netherlands): http://oslifesciences.com/vacancies/biostatistician-6-month-contract-e450-e500-per-day-belgium/   Get in touch for further information about these and other roles – we’re always interested in having a chat. Thanks! Robert Marrett | Head of Life Sciences Recruitment | Optimus Search www.oslifesciences.com | rmarrett@optimussearch.com  UK: Telephone 02030969383 Direct Line | Fax +44 (0) 20 7287 4908 DE: Telefon +49 (0)89 74 11 85 266 | Fax +49 (0) 30 2092 4200

Hi All,I do have below requirement which is for our Direct Client. Please let me know your are interested.Title: Manager -
Biostatistician
Location: Woodcliff Lake, NJ

Duration: Long Term (12+
Months)

Description:

·         Work
with the clinical study team on study design, development and/or review of
clinical study protocols.

·         Develop
and/or review statistical analysis plans, including Table/listing/figure
shells, and final study report for clinical studies;

·         Work
with clinical data managers on design/review of case report form, data transfer
specification, edit check specification, and participation in user acceptance
testing (UAT); generate/review data tables/listings and coordinate data review
meetings during the course of the study to ensure data quality.

·         Oversee
programming activities, perform quality assurance checks on internally or
externally produced SAS tables, listings, and figures, and ensure the quality
of deliverables. Perform post-hoc statistical analyses as needed.

·         May
work on submission teams as a statistician and/or a programmer.

·         Generate
and QC outputs for publications; review publication (abstract/manuscripts) to
ensure accuracy, quality and soundness of statistical methodologies

·         Will
serve as lead Statistician on complex trials and across multiple studies.

·         Project
work including participating in the development of Clinical Development Plans
(CDPs) and the protocol development process, developing and implementing
Statistical Analysis Plans (SAPs), supervising CROs and interfacing with
co-promoters, attending IPT meetings, consulting with clinical or regulatory
affairs groups on strategic issues related to compound development, study
designs, analysis, resource needs and future plans.

·         Managing
non-project work including infrastructure development initiatives and
involvement in committees working to develop SOPs and SWPs to improve quality,
efficiency and timeliness of work processes

 

QUALIFICATIONS NEEDED:

·         Must
have a MS in Biostatistics/Statistics with at least 10 years of experience or a
PhD in Biostatistics/ Statistics with at least 7 years of experience in the
pharmaceutical, CRO or biotech industry.

·         Strong
SAS programming skills.

·         Neuro
experience is required.

·         Ability
to effectively work on multiple projects

·         Good
organization, time management and attention to detail skills needed to work in
a stressful environment under tight deadlines while maintaining focus on details
and quality.

·         Applies
good judgment and leads problem solving within the teamThanks,
Kishore Rao,
Phone : (732) 227-1772 Ext- 413 
Fax: (732) 909 2358

www.ittblazers.com  / Email: kishore@ittblazers.com

Hello everyone! my name is Kingsley i'm new to PhareMed and wanted to know about the network and looking forward to work on project on Statistics and applied statistics 

Searching for a job as data analyst in UK