IVR/IWR for clinical trials • IRT • Randomization • Clinical Supply Chain Management • ePRO
501 - 1000
💰 $1.7M Debt Financing on 2010-03
October 28
🇺🇸 United States – Remote
💵 $90k - $130k / year
⏰ Full Time
🟢 Junior
🧪 Clinical Research
🗽 H1B Visa Sponsor
IVR/IWR for clinical trials • IRT • Randomization • Clinical Supply Chain Management • ePRO
501 - 1000
💰 $1.7M Debt Financing on 2010-03
• Endpoint is an interactive response technology (IRT®) systems and solutions provider that supports the life sciences industry. • The Biostatistician is responsible for the statistical analysis and interpretation of clinical trial data, working closely with cross-functional teams to ensure accurate and meaningful results. • This role involves developing Statistical Analysis Plans (SAPs) and contributing to the randomization process. • They will provide expert consultation on statistical methodologies and collaborate with the Statistical Programming team to ensure the integrity of data analyses and outputs.
• Master’s or PhD in Statistics, Biostatistics, or a related field is required. • Bachelor’s degree with substantial working experience in biostatistics will be considered. • 2+ years of biostatistics experience, preferably in clinical trials. • Proficiency in statistical software such as SAS, R, or Python required. • Experience in the life sciences, regulatory environments, and knowledge of 21 CFR Part 11 and GxP is highly preferred. • Strong statistical knowledge, including experience with survival analysis, mixed models, and longitudinal data analysis. • Excellent problem-solving abilities and attention to detail. • Demonstrated ability to work independently and within cross-functional teams. • Strong written and verbal communication skills, with the ability to clearly present statistical findings. • Familiarity with regulatory requirements for clinical trial data.
• All job offers will be based on a candidate’s location, skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. • Regular, full-time or part-time employees working 30 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), and Company bonus where applicable.
Apply NowOctober 20
51 - 200
Manage clinical trials for CPC, ensuring compliance and effective site operations.
🇺🇸 United States – Remote
💵 $62k - $72k / year
⏰ Full Time
🟢 Junior
🧪 Clinical Research
🗽 H1B Visa Sponsor
October 4
10,000+
Project Manager leading early phase clinical trials at Parexel.
🇺🇸 United States – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🧪 Clinical Research
🚫👨🎓 No degree required
🗽 H1B Visa Sponsor