Statistician Consultant

Remote • Posted 3 hours ago • Updated 31 minutes ago
Contract Independent
Contract W2
12 Months
No Travel Required
Remote
Depends on Experience
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Clinical Research
  • Communication
  • Forms
  • GC
  • JD
  • LinkedIn
  • Management
  • Medical Writing
  • Professional Development
  • Project Management
  • Quality Control
  • R
  • Reporting
  • SAS
  • Statistics
  • Writing

Summary

Job Title:- Statistician Consultant

Location:- Remote

Duration:- 6-12+ months+, conversion to FTE

Visa:- , (must work on w2/1099) (need strong communication)

 

 

Job Description-:

They’re looking for someone who has managed a staff to go along with programming skills in SAS and or R. They also must have worked in CRO environment.

The full JD is below and with submissions please send LinkedIn profiles and two managerial references with work emails.

 

This is a contract-hire opportunity.  The ideal candidate should have demonstrated proficiency with statistical methods and applications in the clinical research with strong programming skills in SAS and or R.

 

 

  • Collaborating with clinical investigators, sponsor, and cross-functional teams to determine study design;
  • Collaborating with Medical Writing and Project Management teams on protocol development, including writing sections pertaining to statistical input;
  • Development of statistical analysis plans and programs to perform analyses and display study data;
  • Reviewing protocols and case report forms to ensure that protocol objectives are met and standards are maintained;
  • Generating treatment allocations in randomized clinical research studies and ensuring proper implementation;
  • Performing statistical analyses; writing and validating application programs, including for centralized monitoring purposes;
  • Implementing data and safety monitoring reports to ensure participants’ safety;
  • Developing metrics and generating quality control reports to optimize the performance of clinical sites and the coordinating center;
  • Generating study reports to be distributed to internal and external monitoring committees and regulatory bodies;
  • Participating in professional development activities both within and outside the company
  • Other duties as assigned

Requirements:

  • Minimum of 3-5 years of experience in a CRO environment
  • Demonstrated proficiency with statistical methods and applications in clinical research.
  • Strong programming skills in SAS and/or R.
  • Ability to manage multiple tasks.
  • Ability to work independently, as well as in a team environment.
  • Ability to effectively communicate technical concepts, both written and oral.

 

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 90859492
  • Position Id: 8982230
  • Posted 3 hours ago
Contact the job poster
Kumar Sai

Kumar Sai

Recruiter @ SumasEdge Corporation
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