Statistical Programmer

Interpublic; England; Hybrid; GBP 45,000 - 65,000; Full time

Job summary

Adelphi Real World is seeking a Statistical Programmer to join the Generate Statistical Programming team. The role focuses on coordinating analytical support for single-sponsor secondary data studies and developing SAPs with robust definitions and analyses.

You will manipulate and analyze real-world data, ensure data integrity, and collaborate with project teams to meet client needs within project timelines.

Qualifications

• Substantial experience and proficient in using statistical software.
• Experience with large, real-world data sources (claims, registries, EMR).
• Strong numerical/analytical skills and attention to detail.
• Excellent written and verbal communication; team player.

Responsibilities

• Coordinate analytical support across single-sponsor secondary studies.
• Draft and finalize SAPs and study protocol sections.
• Write and validate programming code for data manipulation and analysis.
• Coordinate resources with the Gen SP team to ensure timelines.

Tools

Stata

SAS

SPSS

Job description

## Statistical ProgrammerApply: Hybrid: Cheshire, Cheshire, United Kingdom: Full time: Posted Today: R15877**Agency:**Adelphi**Job Function:**Projects and Performance Improvement**Job Subfunction:**Project and Program Management **Job Description:****Statistical Programmer - Adelphi Real World** **Who We Are:**Adelphi Real World is a global consultancy in healthcare. We collect and interrogate real world data to aid the pharmaceutical industry in understanding the management and treatment of specific diseases. This understanding informs the successful development of pipeline assets and the positioning of inline products. Real world data can also be used to leverage Health Outcomes / Economic argumentation through statistically validated publications. **The Role:**To join the Generate Statistical Programming team with a primary focus of coordinating and providing analytical support across all single-sponsor secondary data studies, i.e. conducting complex data manipulation and analysis of existing real-world data sources worldwide to meet clients’ real-world evidence needs. You will work collaboratively with an enthusiastic and cohesive team, supporting various study teams and research projects.**Accountabilities:**Contributing to the design of real-world studies:o Drafting and finalisation of appropriate sections within study protocols (e.g. sample size, statistical methods, data analysis etc.) for review by clients and other review committeeso Development of a robust, transparent and coherent Statistical Analysis Plans (SAPs), incorporating comprehensive operational definitions and/or code lists, statistical methods, objective-specific analyses and table shells, for implementation by yourself or others with limited scope for interpretation. Data management, manipulation and analysis of existing real-world data sources (e.g. claims, registries etc.):o Responsible implementing data management process, i.e. secure storage, logging and data destruction, across all secondary data studieso Writing of programming code to address data manipulation, analysis and output requirements as detailed in the study protocol/ SAP, including quality control (QC) of all code and outputs, and post-review revisions, as per the agreed study timelines. Co-ordination of resources:o Responsible for ensuring all secondary data studies are sufficiently resourced from a statistical/ analytical perspective, including liaison with other senior members of Gen SP team to align on team capacity/ workload.**The person:**• Substantial experience and proficient in using statistical software (e.g. Stata, SAS, SPSS etc.)• Substantial experience of conducting data manipulation and analysis of large, complex, event-level secondary data sources (e.g. claims data, electronic medical records, administrative data, registries etc.)• Hold a good honours degree (2:1 or 1st) in a numeric/ analytical discipline• Experience of contributing towards or developing study protocols and/or SAPs• Knowledge of the pharmaceutical industry• A high level of interpersonal skills and willing to work collaboratively as part of a wider team• A drive to help shape the future structure and success of the S&DA team• Highly motivated with a proactive approach to work and strong problem-solving skills.• A high level of numeracy, analytical, and interpretive skills, with a close attention to detail• Good organisational and time management skills and a flexible way of working• Strong written and verbal communication skills and a confident communicator• Proficient in standard Microsoft packages, e.g. Word, Excel and PowerPoint. The following attributes are not considered essential, but would be preferable in candidates:• Substantial experience and proficient in Stata statistical software• Experience with, or knowledge of, real-world evidence and/or observational studies *To the extent permissible by local law, Omnicom’s policy requires employees to work in the office for a minimum of three days a week, unless additional in-office days are directed by their agency or manager.* Omnicom is committed to hiring and developing exceptional talent. We agree that talent is uniquely distributed, and we’re focused on developing inclusive teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. Join us—we look forward to getting to know you. We will process your personal data in accordance with our Recruitment Privacy Notice. Link to Recruitment Privacy Notice: https://www.omc.com/privacy-notice/