Principal Statistical Programmer

Overview<br><br><p style="text-align: justify;"><span style="font-family: verdana, geneva; font-size: 10pt;">Emmes Group: Building a better future for us all.</span></p><p style="text-align: justify;"> </p><p style="text-align: justify;"><span style="font-family: verdana, geneva; font-size: 10pt;">Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.</span></p><p style="text-align: justify;"> </p><p style="text-align: justify;"><span style="font-family: verdana, geneva; font-size: 10pt;">We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!</span></p><p style="margin: 0px; text-align: justify;"> </p><p style="margin: 0px; text-align: justify;"><span style="font-family: verdana, geneva, sans-serif; font-size: 10pt;"><strong>Primary Purpose</strong></span></p><p style="margin: 0px; text-align: justify;"> </p><p style="margin: 0px; text-align: justify;"><span style="font-family: verdana, geneva, sans-serif; font-size: 10pt;">The Principal Statistical Programmer I provides lead statistical programming support for complex clinical research projects, utilizes advanced SAS programming techniques and offers expert consultation across the company. Key responsibilities include ensuring the use of sound methodologies, delivering key regulatory-compliant output, developing organized programming documentation, writing efficient code, and mentoring staff. This role also provides project updates to management while performing assigned duties and presents internally on statistical programming topics. Expertise in statistical programming techniques and strong communication skills are essential for success in this role.</span></p> <br>Responsibilities<br><br><ul><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Provides lead statistical programming support for multiple complex clinical research study</span><br><span style="font-size: 10pt;">projects or study teams.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Provides advanced statistical programming development with SAS (Base, Macros and SQL) and provides expert consultation to projects across the company including statistical programming methodology.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Ensures that sound methodologies are adopted by establishing advanced knowledge of programming techniques required for clinical trials research which involve either CDISC standards and analysis data sets or production of standard and custom tables listings and figures.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Provides key deliverables based on established advanced knowledge of regulatory requirements for clinical research E-submissions and/or study requirements for Sponsor, Regulatory, Investigator or Safety review meetings.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Develops well organized programming documentation and annotations including specifications, review of mock shells, adhering to relevant Standard Operating Procedures and contributes to standardization efforts.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Writes well-documented, efficient, and high-quality code, conducts code review, supports cross-functional programming activities, and programming validation as needed.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Develops expertise in current statistical programming techniques to develop reproducable code and ensure the adoption of sound methodologies.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Presents statistical programming topics internally and may present at external conferences.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Serves as a mentor to statistical programming staff. </span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Provides project updates to appropriate project management or department management staff.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Other duties as assigned.</span></li></ul> <br>Qualifications<br><br><ul><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">A bachelor's degree plus 6 years or master's/doctoral degree plus 4 years Statistical programming experience as a CDISC/TLF Statistical programmer in Pharmaceutical/CRO environment, education in a scientific discipline preferred.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Understanding of GCP principles and other regulatory standards (e.g. FDA, EMA, and ICH guidance and recommendations) in Clinical Research.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Good analytical skills with the ability to process scientific and medical data.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Ability to manage multiple tasks and priorities independently.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Ability to work independently as well as in a team environment.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Strong skills in prioritization, problem-solving, organization, decision-making, and time management.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Ability to articulate complex and advanced programming and technical concepts through written and oral communication.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Excellent communication, interpersonal and organization skills.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Self-motivated, proactive and detail oriented.</span></li><li style="font-size: 10pt; text-align: justify;"><span style="font-size: 10pt;">Strong statistical programming skills in SAS, familiarity with R, Python or other relevant statistical software considered beneficial.</span></li></ul><p style="margin: 0px; text-align: center;"><span style="text-decoration: underline; font-family: verdana, geneva, sans-serif; font-size: 10pt;"><strong>CONNECT WITH US!</strong></span></p><p style="margin: 0px; text-align: center;"><span style="font-family: verdana, geneva, sans-serif; font-size: 10pt;"><em>Follow us on Twitter - @EmmesCRO</em></span></p><p style="margin: 0px; text-align: center;"><span style="font-family: verdana, geneva, sans-serif; font-size: 10pt;"><em>Find us on LinkedIn - Emmes</em></span></p><p style="margin: 0px; text-align: center;"> </p><p style="margin: 0px; text-align: left;"> </p>