Submitting more applications increases your chances of landing a job.
Here’s how busy the average job seeker was last month:
Opportunities viewed
Applications submitted
Keep exploring and applying to maximize your chances!
Looking for employers with a proven track record of hiring women?
Click here to explore opportunities now!You are invited to participate in a survey designed to help researchers understand how best to match workers to the types of jobs they are searching for
Would You Be Likely to Participate?
If selected, we will contact you via email with further instructions and details about your participation.
You will receive a $7 payout for answering the survey.
Title: Senior/ Principal Statistical Programmer(R) Location: Remote Duration: Long Term Contract Salary: Open Experience : 6-10+ Years Notice : Immediate OR Within 15days If Interested please send your updated resume to: rehana.
j@two95intl.
com and include your rate/Salary requirement along with your contact details with a suitable time when we can reach you.
If you know of anyone in your sphere of contacts, who would be a perfect match for this job then, we would appreciate if you can forward this posting to them with a copy to us.
We look forward to hearing from you at the earliest.
We are looking for Senior / Principal Statistical Programmer(s) with strong hands-on expertise in R (mandatory) and SAS , solid CDISC (SDTM/ADaM) experience, and exposure to regulatory deliverables (TLFs, ISS/ISE, submissions) Mandatory Skills & Experience: 6–10+ years of experience in statistical programming in clinical domain (R/SAS) Strong statistical programming expertise in R (at least 1-3+ Years) Hands-on SAS programming experience required Working knowledge of SQL and/or Python is an advantage Experience with data reuse, historical trial data, Real-World Data (RWD), biomarker data, and External Control Arms Core Responsibilities: End-to-end statistical programming for ADaM datasets and Tables, Listings, and Figures (TLFs) Programming support for ISS, ISE, regulatory submissions, and RTQs Implementation, validation, and maintenance of CDISC SDTM and ADaM standards Development and reuse of macros, functions, and programming utilities Authoring and application of metadata specifications and derivations Advanced (Good to have) Experience: Experience in Oncology, Respiratory, or Immunology, along with RWD/RWE exposure, is a strong plus.
Experience with RWE oncology datasets (EHR, claims data) Building and validating analysis cohorts Hands-on experience with survival analysis and propensity score methods
You'll no longer be considered for this role and your application will be removed from the employer's inbox.