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Verna scientific 
Industry Pharma/Biotech/
Company Type Staffing firm
 
 

 
Job Search Results: Jobs 1 - 4 of 4  View Titles Only  Page 1 of 1
 
Title   Company Name     Location   Date  
Statistical (SAS) Programmer 

  Verna scientific    All, Irvine   28/6/2007 
Category: Life Sciences  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Biostatistics, GLP, GMP  
Description:
Urgent requirement for one of the our top client located in 'CA.

Position Description:

This position will provide statistical programming support under the direction of the senior staff for the creation, quality control, documentation and maintenances of analysis data set, tables, listings and graphs.  
Requirements:
Requirements:

Education or education/experience combination equivalent to a post graduate degree in Computer Science, Life Science, Statistics or Statistic related field. One (1) years of pharmaceutical clinical research experience with Masters degree or Masters equivalent, or two (2) years of pharmaceutical clinical experience with a Bachelors degree or Bachelors degree equivalent.
General knowledge of medical terminology and clinical trial methodologies
Working knowledge of Base SAS, SAS/STAT; SAS Macro language a plus
Good analytical and problem solving skills
Excellent English communication skills (verbal and written) as well as good interpersonal skills
Focused, well organized, detail-oriented
Works well under pressure, with initiative to take on unfamiliar tasks.
Works well in a team environment.

Contact:

The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us to bob.harold@vernascientific.com  
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SAS Programmer 

  Verna scientific    North Area, Jersey City   11/6/2007 
Category: QA - Quality Control  
Education: Bachelors   Position type: Full Time Employee  Experience: 3 years 
Area(s) of expertise desired: Biostatistics, SAS  
Description:
Are you looking for professional growth opportunities as a full time employee enjoying OUTSTANDING BENEFITS? Do you have 1-4 years of professional experience in the biotech/pharmaceutical industry? We offer a rare opportunity to work within an organization where individual contribution makes a significant difference.

What Youll be Doing:

1-4 years of pharmaceutical/CRO experience as a SAS programmer

- Degree in Statistics or related field

- Phase II-IV clinical trial experience

- Safety and some efficacy experience

- Good understanding of the clinical process

- Good understanding of important study documents (e.g. Protocol, Case Report Forms, Statistical Analysis Plan)

- Good communication skills

- Any additional qualifications will be considered a plus (e.g. integration experience, handling FDA and marketing requests)

How to Reply

The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us
to bob.harold@vernascientific.com

No Time to send out your Resume? Current Employed but Still Looking for a New Job? Just send your contact details and let our recruiters contact you
 
Requirements:
Minimum of 1-4 year pharmaceutical/CRO experience as a SAS programmer  
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Statistician - Validation/Process 

  Verna scientific    All, Swiftwater   6/6/2007 
Category: perm  
Education: Masters   Position type: Full Time  Experience: 3 years 
Area(s) of expertise desired: GLP, GMP, Laboratory, Quality Control, Validation  
Description:
Responsible for providing statistical support for validation, qualification, and comparability experiments, as well as performing data analysis upon protocol execution. Will support QC in method trending and provide statistical support for laboratory investigations as needed.  
Requirements:
We are an equal opportunity employer M/F/D/V Education/Years Experience/Other Skills : MS in Statistics, Minimum 3-5 years related experience in GxP environment
Requires cGMP/cGLP training and strong writing skills along with excellent statistical, analytical and computer skills.
 
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Senior Director of Clinical Development 

  Verna scientific    All, mountain view, CA   19/1/2007 
Category: Life Sciences  
Education: Doctorate   Position type: Full Time Employee  Experience: 5 years 
Area(s) of expertise desired: Biochemistry, Bioinformatics, Biology, Biophysics, Biostatistics, Pharmacokinetics, Pharmacology  
Description:
Responsible for all medical aspects, medical monitoring, meeting Regulatory Authority requirements, develops clinical protocols, publish, manages CRO staff, Drug Safety Service/Global Pharmacovigilance Department, Post Marketing Surveillance campaigns, interfacing with sites, vendors, investors, collaborators, customers, Regulatory Authorities and Board of Directors.

supervises biostatistical support, Clinical Program Managers (CPMs) & Clinical Research Associates (CRAs) and other clinical staff.

Acts as safety monitor for all clinical programs.

Plans and builds fully integrated Drug Safety Service (Pharmacovigilance) for products marketed or co-marketed.

Responsible for oversight of all clinical safety reports and updates to all regulatory authorities and IRBs/IECs, as well as Annual IND updates, IB revisions, protocol (safety) amendmentsl, and input to ISS (ISEs) for NDAs.
 
Requirements:
Education: MD degree is required with Minimum 5 years of experience in clinical development and all aspect of clinical trials.  
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