Design Manager

Johnson & Johnson; Hartford; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading global healthcare company is seeking an Experienced Clinical Programmer in Hartford, United Kingdom. You will oversee clinical data management activities, ensuring quality and compliance through robust programming and reporting solutions. The ideal candidate will have a strong understanding of data structures and clinical trial processes. This is an opportunity to significantly impact clinical trials and data oversight in a dynamic environment.

Qualifications

• In-depth knowledge of industry standards and complex data structures.
• Proven technical capabilities in leading clinical trial activities.
• Experience creating and executing edit check programs.

Responsibilities

• Accountable for clinical programming trial activities.
• Review project requirements and documentation comprehensively.
• Ensure utilization of latest standards and technologies.

Skills

Clinical trial programming

Data management

Programming languages

Reporting solutions

Quality control

Job description

The Experienced Clinical Programmer is an experienced clinical trial programmer with in-depth knowledge in industry standard and complex data structures, programming languages, and/or reporting solutions with proven technical capabilities in leading clinical trial activities and/or teams in accordance with departmental processes and procedures. The position is responsible for oversight or the development of one or more clinical data management trial activities of moderate to high complexity/criticality. Including data model specifications, data stream integrations and transformation of source to internal data models and/or CDISC submission ready SDTM tabulation packages (aCRF, define.xml, cSDRG, etc). Creates and executes edit check programs, listings and report solutions to aid in monitoring of safety, risk, compliance and ensures quality data review. Performs reporting solutions role creating study-specific reports translating clinical study team needs into specifications aggregating clinical data sources into custom data and report to monitor safety, risk and compliance.

Responsibilities

• Accountable for one or more clinical programming trial activities of moderate to high complexity, scope and/or criticality.
• Performs comprehensive review of, and provides input into, project requirements and documentation. Identifies gaps, proposes solutions and applies expertise to improve efficiency of programming tasks and/or improve overall quality of programming deliverables.
• Ensures latest standards are being utilized, current technologies are deployed.
• Create and/or review specifications for mapping internal data review model for fit for purpose reporting and/or as well as submission ready CDISC SDTM. Design mapping algorithms for nonstandard conversions.
• Responsible for creation or review of internal data model for fit for purpose reporting consumption and/or submission ready CDISC SDTM packages for health authority submissions and keeping abreast in changing regulatory requirements. Program, or oversight of quality review checks, study specific reports for use by team members and consumers of data.
• May perform role that programmatically aggregates clinical data sources into custom data model for fit for purpose consumption study specific report solutions performing appropriate quality control and verification in support of assigned reporting activities.