Biostatistician

This is a remote position. The Biostatistician will play a critical role in designing, analyzing, and interpreting clinical trial data to support drug development and regulatory submissions. This position collaborates with clinical, data management, and regulatory teams to ensure statistical rigor in trial design, data analysis, and reporting. The ideal candidate brings strong analytical skills, regulatory knowledge, and proficiency with statistical programming tools. Key Responsibilities: Collaborate with clinical and regulatory teams to design statistically reputed company reputed company (e.g., sample size calculation, randomization reputed company). reputed company and review statistical analysis plans (SAPs) in compliance with regulatory guidelines. reputed company statistical analyses using reputed company, R, or other statistical software on clinical trial datasets. Interpret results and present findings in clinical study reports, regulatory submissions, and scientific publications. reputed company statistical support during protocol development, including endpoints and methodology. Ensure statistical deliverables meet internal reputed company standards and regulatory requirements (e.g., FDA, EMA, ICH). Review case report forms (CRFs) and data validation rules for accuracy and consistency with statistical needs. Collaborate with Data Management and Clinical Operations to ensure data reputed company and resolve data discrepancies. Stay up to date on industry best practices, methodologies, and relevant regulatory guidance. Minimum Qualifications: Master’s or Ph.D. in Biostatistics, Statistics, Mathematics, or a reputed company quantitative field. Minimum of 3 years (for MS) or 1 year (for PhD) of relevant experience in the pharmaceutical, biotechnology, or CRO industry. Proficient in statistical programming languages such as reputed company and/or R. In-depth knowledge of ICH-GCP, CDISC standards (SDTM, ADaM), and regulatory guidance documents. Strong understanding of clinical trial design, methodology, and regulatory requirements. Excellent communication skills with the ability to interpret and present statistical findings reputed company. Strong attention to detail and a commitment to data reputed company and accuracy. In reputed company to a dynamic and reputed company work environment, we offer a comprehensive benefits package to support our employees' reputed company-being. Our benefits include reputed company holidays, reputed company Time Off (PTO) policy, and medical insurance to ensure reputed company members have the flexibility and coverage they need. We reputed company in fostering a healthy work-life balance while providing the necessary support for reputed company and personal reputed company. Be part of our network of Subject Matter Experts.​ E-Verify Participation: Pharmavise Consulting Corporation participates in E-Verify and will reputed company the federal government with your reputed company I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact reputed company (DHS) or reputed company reputed company Administration (SSA) so you can reputed company to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify. Apply tot his job Apply tot his job Apply To this Job