Biostatistician

Santa Clara, CA

Contract

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OVERVIEW

Our client is looking for a highly qualified and skilled professional for the role of Biostatistician.  This is for a leading CRO company in Santa Clara, CA.  Our client is open to hiring a qualified Biostatistician levels I-IV dependent on experience.   

RESPONSIBILITIES 

  • Responsible for the design, modification and evaluation of a technical infrastructure relative to analysis of clinical data to support clinical trials
  • Performs statistical analysis and develops tracking systems to determine the efficiency of clinical trials
  • Interacts with clinical investigators to determine protocol design including calculating sample size requirements
  • Drafts statistical analysis plans and table, listing and figures shells
  • Drafts randomization plans
  • Drafts specifications for SAS programming of tables, listings and figures
  • Maintains expertise in state-of-the-art data manipulation and statistical analysis techniques
  • Communicates with clients verbally and in writing to specify requirements and interpret results and statistical analyses

CANDIDATE REQUIREMENTS (Level I - IV)

Level I
Responsibilities

  • Works on problems of moderate scope
  • Exercises judgment within defined procedures and practices to determine appropriate action
  • Interacts under supervision with Sponsors and clinical investigators

Qualifications: A Master degree in biostatistics or equivalent is required. SAS programming experience is preferred

Level II
Responsibilities

  • Works on problems of diverse scope
  • Exercises independent judgment within broadly defined procedures and practices to determine appropriate action
  • Works with little instruction. Executes statistical analysis plans

Qualifications: A Masters/PhD or equivalent experience and 2-5 years’ experience in the pharmaceutical, biotech or medical device industry is required. SAS programming and clinical data experience is required

Level III
Responsibilities

  • Works on complex problems. 
  • Exercises independent judgment within broadly defined procedures and practices to determine appropriate action
  • Identifies deficiencies or enhancements of standard procedures and develops solutions
  • Independently determines methods and procedures
  • May provide guidance to others
  • Executes or oversees executing of statistical analysis plans

Qualifications: A Masters/PhD or equivalent experience and 5-7 years’ experience in the pharmaceutical, biotech or medical device industry is required

Level IV

Responsibilities

  • Works on the most complex problems
  • Exercises independent judgment in developing procedures and practices
  • Handles work independently, and provides guidance to others
  • Executes or oversees executing of statistical analysis plans

Qualifications: A Masters/PhD or equivalent experience and at least 8 years’ experience in the pharmaceutical, biotech or medical device industry is required. Most senior position

About Advanced Clinical

Advanced Clinical is an award-winning clinical development organization that provides global services including CRO, Functional Support, Quality & Validation, Patient Recruitment and Retention, and Strategic Talent Acquisition solutions for pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Our mission is to deliver a truly better clinical experience for our clients and candidates. To learn more about Advanced Clinical which has been named to Chicago Tribune’s Top Workplaces, Chicago’s Best and Brightest Companies, and Best of Staffing Talent & Client, visit http://www.advancedclinical.com.

Regarding your application

Please know that every completed application is carefully reviewed by the Advanced Clinical recruitment team. We understand the time commitment that is needed to prepare an application, so we respect your effort by thoughtfully reviewing and responding to each application. In return, we ask for your patience as careful review takes time, and we may not be able to respond to every application 

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