CONFLUX SYSTEMS is Hiring a Lead Statistical Programmer with R & SAS Expertise Near Bridgewater, NJ
DescriptionYou will provide technical expertise as an experienced R programmer, developing process methodologies to meet the needs of internal and external clients. This role involves planning and coordinating the development of integrated programming solutions that address a full spectrum of statistical programming needs. You will also offer technical leadership and internal consulting services, including specifications and user needs analysis for complex projects or client requirements. Key Skills
Expertise in R programming and SAS Base, with good knowledge of SAS Graph and SAS Macros.
Ability to implement advanced statistical procedures as specified by biostatisticians.
Excellent knowledge of CDISC standards (SDTM and ADaM).
Thorough understanding of relational database components and theory.
Strong application development skills and understanding of clinical trial data.
Proficient in data manipulation, analysis, and reporting of analysis results.
Familiarity with ICH E6, ICH E3, ICH E8, ICH E9, and clinical research processes.
Minimum of 4 years of experience in Statistical Programming within the pharmaceutical or medical devices industry.
Strong verbal and written communication skills.
Ability to manage multiple projects while planning, organizing, and prioritizing activities.
Responsibilities
Perform all responsibilities associated with the Senior Programmer role.
Assist Sr. Programmers and Programmers in their daily activities.
Act as an escalation point for Sr. Programmers and Programmers.
Communicate regularly with sponsors regarding programming progress and proactively address issues.
Provide input and/or write programming specifications.
Serve as a subject matter expert on all aspects of SAS programming.
Understand pharmaceutical industry standards and trends, proactively planning and implementing solutions.
Develop consistent practices for clinical and statistical review of outputs and mentor programming staff.
Check for consistency across therapeutic areas.
Identify, plan, and oversee the implementation of process improvement initiatives.
Maintain expertise in SAS Macros and determine macro development priorities.
Undertake other responsibilities as defined by senior management on an ad-hoc basis.
Required Knowledge, Skills, & Abilities
Experience as a technical team lead, engaging clients and coordinating tasks within a programming team.
In-depth knowledge of clinical research regulatory requirements, including Good Clinical Practice (GCP) and ICH guidelines.
Knowledge of statistics, programming, and the clinical drug development process.
Advanced knowledge of R programming and SAS tools (SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL).
Experience with SDTM and ADaM implementation according to CDISC Standards.
Strong organizational, interpersonal, leadership, and communication skills.
Ability to independently manage multiple tasks and projects, and delegate work effectively.
Excellent attention to detail and problem-solving skills.
Ability to lead teams and projects at a group level, recognizing when negotiation skills are needed.
Ability to establish and maintain effective working relationships with co-workers, managers, and clients.
Required Education & Experience
Bachelor’s degree required, preferably in science or mathematics-related fields.
Minimum of 3 years of experience in Statistical Programming within the pharmaceutical or medical devices industry.