4 days ago
• Lead large global clinical studies • Provide statistical input and planning for multiple studies • Supervise and train junior biostatisticians • Develop Statistical Analysis Plans and conduct analyses • Prepare and review randomization specifications
• Master’s degree or higher in Biostatistics or related field • 8+ years of experience or equivalent combination of education/experience • Minimum 2 years of Oncology experience across Phase I, II, III • Experience with Survival Analysis, Stat lead experience for NDA submission studies • Ability to program in one or more statistical software packages (SAS®) • Proven ability to effectively communicate statistical concepts • Good knowledge of the overall clinical trial process
• Comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD • 401(K), ESPP • Paid time off (PTO) or Flexible time off (FTO) • Company bonus where applicable
Apply Now5 days ago
51 - 200
Contribute to clinical trials design and reporting for Immunovant's autoimmune treatments.
October 22
11 - 50
Statistical support for clinical development at Precision Medicine Group.
October 22
1001 - 5000
Provides statistical support for clinical development at Precision Medicine Group.
🇺🇸 United States – Remote
💵 $113k - $152.8k / year
💰 $35.2M Venture Round on 2021-03
⏰ Full Time
🔴 Lead
🧪 Clinical Research
🗽 H1B Visa Sponsor
September 15
10,000+
Client Relationship Director at Parexel drives sales growth and account profitability.