Statistical Programming Contractor

<p style="text-align:left"><u><b>Job Description:</b></u></p><p style="text-align:inherit"></p><p><b><span>Company Overview</span></b></p><p><span>Since its inception over a decade ago, CRISPR </span><span><span><span><span><span><span><span><span><span><span><span>Therapeutics has</span></span></span></span></span></span></span></span></span></span></span><span> transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR </span><span><span><span><span><span><span><span><span><span><span><span>Therapeutics has</span></span></span></span></span></span></span></span></span></span></span><span> established strategic partnerships with leading companies including Vertex </span><span><span><span><span><span><span><span><span><span><span><span>Pharmaceuticals. CRISPR</span></span></span></span></span></span></span></span></span></span></span><span> Therapeutics AG is headquartered in Zug, Switzerland, with its </span><span><span><span><span><span><span><span><span><span><span><span>wholly-owned U.S. subsidiary, CRISPR</span></span></span></span></span></span></span></span></span></span></span><span> Therapeutics, Inc., and R&amp;D operations based in Boston, </span><span><span><span><span><span><span><span><span><span><span><span>Massachusetts and San</span></span></span></span></span></span></span></span></span></span></span><span> Francisco, California.</span></p><p></p><p><b>Position Summary</b></p><p>The Statistical Programming Contractor will provide technical support for statistical programming activities for assigned clinical studies, FDA submissions, and the development of initiatives.</p><p></p><p><b>Responsibilities</b></p><ul><li>Design, develop, evaluate, validate and modify computer programs using SAS to analyze and evaluate clinical data. </li><li>Have thorough knowledge of CDISC theory and implementation guidelines, able to create and validate CDISC standard datasets</li><li>Program edit checks and produce quality tables, figures and listings in a timely fashion and high quality.</li><li>Work closely with Clinical Operations, Data Management and Biostatisticians on various clinical projects so that data analysis can be performed in a timely fashion.</li></ul><p><b>Minimum Qualifications</b></p><ul><li>Bachelor’s Degree in Statistics, Mathematics, and/or Computer Science/IT background. Master’s Degree preferred.</li><li>Minimum 3 years of statistical programming in a pharmaceutical/biotech or CRO setting (depending on level)</li><li>Strong knowledge in CDISC including SDTM, ADaM, metadata, controlled terminologies, and data flows, as well as in industry standards for electronic submission of data to FDA.</li><li>Strong hands-on SAS programing skills and working experience for clinical trial reporting for SDTM, ADaM, Table, figure, and Listing.</li><li>Excellent working knowledge of SAS/BASE, SAS/STAT, SAS/GRAPH and SAS Macro language.</li><li>Advanced knowledge of GCP/ICH standards, 21 CFR Part 11.</li></ul><p><b>Preferred Qualifications</b></p><ul><li>Strong ability to work within cross-functional teams.</li><li>Excellent interpersonal, organizational, and multi-tasking skills.</li></ul><p></p><p><b>Competencies</b></p><ul><li><span>Collaborative – Openness, One Team</span></li><li><span>Undaunted – Fearless, Can-do attitude</span></li><li><span>Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.</span></li><li><span>Entrepreneurial Spirit – Proactive. Ownership mindset.</span></li></ul><p></p><p><span>CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.</span></p><p></p><p>Base pay range of $70.00 - $80.00 per hour.</p><p></p><p>The hourly rate provided is the reasonable estimate for this contract position. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.</p><p></p><p></p><p><span>CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person&#39;s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. </span></p><p></p><p><span>To view our Privacy Statement, please click the following link:</span> <a href="http://www.crisprtx.com/about-us/privacy-policy" target="_blank">http://www.crisprtx.com/about-us/privacy-policy</a></p>