- Senior
Emmes Group: Building a better future for us all.
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.
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!
Primary Purpose
The Senior Statistical Programmer provides lead statistical programming support for multiple clinical projects using SAS and provides expert consultation across the company. Key responsibilities include delivering key regulatory-compliant output, developing programming documentation, writing efficient code, staying updated on programming techniques, and mentoring staff. The role also includes providing project updates to management while performing assigned duties and presents internally on statistical programming topics.
Responsibilities:- Provides lead statistical programming support for multiple clinical research study projects or study teams.
- Provides statistical programming development with SAS (Base and Macros) and provides expert consultation to projects across the company including statistical programming methodology.
- Ensures that sound methodologies are adopted by establishing proficiency 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.
- Provides key deliverables based on established profiency of regulatory requirements for clinical research E-submissions and/or study requirements for Sponsor, Regulatory, Investigator or Safety review meetings.
- Develops programming documentation and annotations including specifications, review of mock shells, adhering to relevant Standard Operating Procedures and may contribute to standardization efforts.
- Writes well-documented, efficient, and high-quality code, conducts code review, supports cross-functional programming activities, and programming validation as needed.
- Keep abreast of current statistical programming techniques to ensure the adoption of sound methodologies.
- Presents statistical programming topics internally and may present at external conferences.
- Serves as a mentor to statistical programming staff.
- Provides project updates to appropriate project management or department management staff.
- Other duties as assigned.
Qualifications:
- A bachelor's degree plus 4 years Statistical programming experience as a CDISC/TLF Statistical programmer in Pharmaceutical/CRO environment, education in a scientific discipline preferred.
- Understanding of GCP principles and other regulatory standards (e.g. FDA, EMA, and ICH guidance and recommendations) in Clinical Research.
- Good analytical skills with the ability to process scientific and medical data.
- Ability to manage multiple tasks and priorities independently.
- Ability to work independently as well as in a team environment.
- Strong skills in prioritization, problem-solving, organization, decision-making, and time management.
- Ability to articulate complex programming and technical concepts through written and oral communication.
- Excellent communication, interpersonal and organization skills.
- Self-motivated, proactive and detail oriented.
- Strong statistical programming skills in SAS, familiarity with R, Python or other relevant statistical software considered beneficial.
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