Biostatistical Analyst Salary at Biopier Inc BETA

Associate Director, Biostatistics We are looking for an experienced Associate Director, Biostatistics to lead statistical strategy, analysis, and oversight for clinical development programs. This role supports high-profile projects while managing a team of biostatisticians to ensure the highest quality and compliance with regulatory standards. Key Responsibilities: Strategic Leadership: Collaborate with cross-functional teams to develop statistical strategies for clinical trials (Phases I-IV). Provide input on protocol design, sample size calculations, and endpoint selection. Contribute to regulatory submissions and respond to agency queries. Team Management & Mentorship: Lead and mentor a team of biostatisticians, fostering growth and professional development. Assign resources, delegate tasks, and monitor project progress. Conduct performance reviews, provide constructive feedback, and develop training plans. Operational Oversight: Oversee the development of statistical analysis plans

ALS, on behalf of one of our trusted CRO partners, is seeking a Real World Statistics Contractor to support a range of observational studies and real-world evidence (RWE) projects. This is a fantastic opportunity for an experienced statistician to contribute their expertise in a collaborative, fast-paced environment. Key Responsibilities: Lead all scientific and operational statistical activities for assigned studies—ranging from observational research and real-world data (RWD) analyses to clinical trials. Provide expert input on study protocols, including reviewing study design and statistical methodologies, conducting analyses, and interpreting complex data with support where needed. Represent Real World Statistics in cross-functional Study Execution Teams, offering strategic and technical statistical guidance across multiple projects. Collaborate effectively with stakeholders across Health Economics & Outcomes Research (HEOR), Medical Affairs, Clinical Development, and RWE teams. Su

Early Career Opportunity in Drug Development Data Science and Analytics Company: BioPier, LLC. (a Veramed Company) Location: Burlington, MA Position: Statistical Programming and Biostatistics Type: Full-time Brief Description: BioPier, LLC., a Veramed company, is seeking highly motivated, inquisitive, coachable and skilled programmers. We prefer a master’s degree or higher in STEM disciplines, who have strong programming, analytical, and data science skills and are looking to launch their careers in the fast-growing field of drug development and clinical data science. This position offers a unique opportunity to work alongside the talented BioPier team, receive hands-on training, and contribute to high-impact projects in the clinical and biostatistics domain. This is a paid, full-time benefit eligible position. Position Responsibilities: Statistical Programming: · Conduct Phase I-IV Clinical Study Reports (CSRs) to evaluate study safety and efficacy · Work on data science and standardi

Statistical Programmer (AD/Director Level) - Contact Location: Boston, MA (Hybrid – 2 days onsite/week) Our client, an innovative biopharmaceutical company based in Boston, is seeking an experienced AD/Director Statistical Programmer to support critical statistical analyses for clinical programs, including regulatory submissions, safety monitoring, and clinical study reports (CSRs). This role offers the opportunity to make a significant impact within a growing Biostatistics & Biometrics team. Key Responsibilities: Develop, validate, and maintain SAS programs for generating tables, listings, and figures (TLFs) from clinical trial data Perform QC checks and double programming for regulatory submissions (NDA/BLA) Provide statistical programming support for medical affairs initiatives, including publications and presentations Collaborate with biostatisticians to implement Statistical Analysis Plans (SAPs) and conduct ad-hoc analyses Leverage expertise with MediReal (or demonstrate the abil

Responsibilities: Provide statistical input for protocol development, study design, and CRF development, actively contributing to internal and client meetings, and discussing sample size scenarios. Conduct sample size calculations and draft statistical methodology sections for study protocols. Oversee the production and quality control of randomization schedules, statistical analysis plans, reports, and other supporting documents. Design statistical analysis plans and table shells for study protocols or integrated summaries for NDA submissions. Develop SAS programs for generating and quality-checking statistical tables, figures, and listings. Perform mapping from raw datasets to CDISC SDTM datasets. Produce and quality control define.pdf, define.xml, and annotated case report forms for SDTM submission. Develop SAS programs to generate and validate analysis datasets in CDISC ADaM or sponsor-specified formats. Review and contribute to the statistical and results sections of clinical stud

Senior/Principal Biostatistician - Permanent - Cambridge, MA (Hybrid) Proclinical is partnered with a truly exciting Biotech at the forefront of innovation within the Oncology space. The business is placing strong investment into the growth of their Biostatistics function with a specific focus on further developing the team in their US headquarters. Primary Responsibilities: You will be responsible for all statistical aspects of clinical trials, ensuring methodologies and analyses are robust and aligned with scientific objectives. Your role involves strategic collaboration with cross-functional teams and oversight of CROs to guarantee high-quality statistical deliverables. Skills & Requirements: Degree in statistics or a related field. Expertise in statistical analysis within clinical trials, with oncology experience being advantageous. Proficiency in statistical software such as SAS and R. The Senior/Principal Biostatistician's responsibilities will be: Lead statistical activities for

Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. The Dana-Farber Cancer Institute seeks an Biostatistician with a focus in large data sets and machine learning who will work within the Hale Family Center for Pancreatic Cancer Research ( http://halecenter.dfci.harvard.edu) .The Hale Family Center for Pancreatic Cancer Research focuses on Pancreati

We are hiring a Statistical Programmer Consultant on a contract basis. This role will be remote based. This is a W2 position. The Consultant will provide timely support to the project team on all statistical programming matters according to the project strategy. Programs SDTM/ADaM/TLFs for the studies, write datasets specification, QC datasets and tables. Identifies and communicates changes in project requirements that may affect key deliverables. Responsibilities Involved in the programming activities on multiple projects/ studies across various therapeutic areas, both internally and externally by CROs Creates and reviews annotated CRF to SDTM datasets Provides support in balancing conflicting priorities, promoting communication and adequate information flow to motivate, encourage and align people with the company' s strategic objectives Functions as a positive role model for setting high expectations for quality, creativity and project ownership Works collaboratively with Clinical Op