Principal Statistical Programmer

AECOM; Miami (FL); Remote; USD 106,000 - 244,000; Full time

Job summary

AECOM is seeking a Principal Statistical Programmer to join their FSP team. This home-based role includes planning and coordinating statistical programming solutions across various therapeutic areas, requiring expertise in R and SAS, along with strong communication and leadership skills. Ideal candidates have over 7 years of experience in the pharmaceutical industry and a Bachelor's degree in a relevant field. Join a leading company to make a significant impact in clinical research.

Qualifications

• 7+ years experience in statistical programming in pharmaceutical/medical devices.
• Expertise in SAS and R with strong understanding of statistical procedures.
• Excellent verbal and written communication skills.

Responsibilities

• Program, test, and document statistical programs for studies.
• Interpret requirements and develop programming specifications.
• Lead technical team meetings and manage project timelines.

Skills

R programming

SAS Base

CDISC standards

Clinical trial data analysis

Statistical programming

Education

Bachelor's degree in science/mathematics

Tools

SAS/BASE

SAS/STAT

SAS/GRAPH

SAS/MACRO

Job description

**Location: Homebased anywhere in the US**

**Purpose:**

Join our FSP team today! In this role you will plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.

**Job Details:**

+ Position: – Principal Statistical Programmer

+ Home Based

+ Min 7+ years of CRO/Pharma Industry

+ Therapeutic Areas: Oncology // Immunology // IDV // EDCP

**Key Skills:**

+ Must have expertise of R programming as well as SAS Base, and good knowledge of SAS graph and SAS Macros.

+ Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician.

+ Must have excellent knowledge of CDISC standards (SDTM and ADaM)

+ Thorough understanding of relational database components and theory.

+ Excellent application development skills.

+ Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.

+ Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes.

+ Minimum of 7+ years of experience in Statistical Programming in pharmaceutical or medical devices industry

+ Good verbal and written communication skills.

+ Ability to work on multiple projects, plan, organize and prioritize activities.

**Required Knowledge, Skills and Abilities:**

+ Experience as technical team lead directly engaging clients and coordinating tasks within a programming team

+ In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

+ Knowledge of statistics, programming and/or clinical drug development process

+ Advanced knowledge of R programming

+ Base SAS, SAS/STAT, SAS Graph and SAS Macro Language

+ Should have experience with SDTM Implementation and ADaM implementation according to CDISC Standards.

+ Must have expertise in SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL.

+ Good organizational, interpersonal, leadership and communication skills

+ Ability to independentlymanage multiple tasks and projects

+ Ability to delegate work to other members of the SP team

+ Excellent accuracy and attention to detail

+ Ability to delegate work to other members of the SP team [SPM]

+ Exhibits routine and occasionally complex problem-solving skills

+ Ability to lead teams and projects and capable of managing at a group level

+ Recognizes when negotiating skills are needed and seeks assistance.

+ Ability to establish and maintain effective working relationships with co-workers, managers and clients.

**Responsibilities:**

+ Perform, plan co-ordinate and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically..

+ Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies.

+ Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies.

+ Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.

+ Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.

+ Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.

+ Use and promote the use of established standards, SOP and best practices.

+ Provide training and mentoring to SP team members and Statistical Programming department staff.

**MINIMUM REQUIRED EDUCATION AND EXPERIENCE:**

+ Bachelor's degree from reputable university preferably in science/ mathematics related fields

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $106,200.00 - $243,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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