Study Lead Statistician (Product Facing)

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Study Lead Statistician (Product Facing) with a 1-year contract, paying $90–$110/hour. Remote work is preferred for U.S.-based candidates. Key skills include R and SAS programming, clinical trial experience, and statistical leadership.
🌎 - Country
United States
💱 - Currency
$ USD
💰 - Day rate
Unknown
Unknown
880
🗓️ - Date discovered
April 23, 2025
🕒 - Project duration
More than 6 months
🏝️ - Location type
Remote
📄 - Contract type
W2 Contractor
🔒 - Security clearance
Unknown
📍 - Location detailed
United States
🧠 - Skills detailed
#Programming #Statistics #Strategy #Visualization #Datasets #R #Leadership #ADaM (Analysis Data Model) #DMC #SAS
Role description

🔍 We're Hiring: Study Lead Statistician (Product Facing) – REMOTE | 🔍

Are you a highly analytical biostatistician with experience across the full spectrum of clinical drug development? Ready to lead statistical strategy for clinical studies at one of the world’s leading biotech companies?

One of our Biotech customers is looking for a Study Lead Statistician to join their team.

Role: Study Lead Statistician (Product Facing)

📍 Location: Remote – U.S. based (PST Preferred)

💼 Unit: General Medicine

🕒 Duration: 1 Year (with potential extension)

💰 Pay: $90–$110/hour (W2)

🌟 About the Role:

As a Study Lead Statistician (SLS), you’ll be a critical partner in the design, analysis, and strategy of customer’s clinical trials. You’ll collaborate across functions, provide key statistical insights, and ensure scientific integrity throughout the product life cycle—from pre-clinical to post-marketing.

This is not a programmer role—we’re seeking a statistician who leads with expertise, confidence, and vision.

✅ What You’ll Do:

   • Lead statistical activities for clinical studies with minimal supervision

   • Provide input to protocols, SAPs, TFL shells, DMC charters, and randomization specs

   • Oversee QC of ADaM datasets and statistical analyses (primary/key endpoints)

   • Contribute to CRF development, IVRS reviews, DLRMs, and study-level deliverables

   • Analyze data to support publications, study planning, and regulatory responses

   • Supervise and mentor Study Statisticians

   • Collaborate with cross-functional stakeholders (programming, clinical, medical writing)

🎯 Ideal Candidate:

   • M.S. in Biostatistics/Statistics with 3–6+ years of experience (Ph.D. with 3–5+ years also welcome)

   • Strong R and/or SAS programming skills (especially simulations)

   • Experience in clinical trial design, analysis, and reporting

   • Confident communicator – able to clearly explain statistical findings and contribute to cross-functional teams

   • Prior experience in Life Cycle Drug Development is a big plus

   • R-Shiny app development or Bayesian modeling? Even better!

💼 Top Skills We’re Looking For:

   • R programming proficiency (along with SAS)

   • Simulation & data visualization experience

   • Proactive, collaborative, and solution-oriented mindset

   • Strong analytical and statistical judgment – not just coding!

🚫 Red Flags:

   • No clinical trial or drug development experience

   • Pure SAS programming background without statistical leadership

   • Inability to articulate past contributions

   • Passive attitude or lack of initiative

👉 Apply now to be a driving force in the future of medicine.

#Biostatistics #StudyLeadStatistician #ClinicalStatisticians #ClinicalTrialStatistics #StatisticalLeadership #RProgramming #SASProgramming #DataSimulation #RShiny #BayesianStatistics #PharmaJobs #BiotechCareers #ClinicalDevelopment #DrugDevelopment #LifeSciences #RemoteJobs #HiringNow #JobOpportunity #HealthcareInnovation

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