Assoc Clin Programmer

Johnson & Johnson are currently seeking a Associate Clinical Programmer, Clinical Programming to join our Integrated Data Analytics & Reporting (IDAR)Department.

This position is based in High Wycombe (Hybrid).

Remote work options in the UK may be considered on a case-by-case basis and if approved by the company.

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at https:// www.jnj.com/.

Position Summary

The Associate Clinical Programmer is a clinical trial programmer with basic knowledge in data structures, programming languages, and/or report solutions who supports clinical programming trial activities and/or teams in accordance with departmental processes and procedures.

The position is responsible for review of project specification and documentation, verification of internal data models and/or CDISC submission ready SDTM tabulation packages (aCRF, define.xml, cSDRG, etc).

Develop, verification and documentation of edit check programs, listings and report solutions to aid in monitoring of safety risk, compliance and ensures quality data review.

This position is a member of the clinical programming team and is capable of supporting programming activities with guidance and may contribute to departmental innovation and process improvements.

Role and responsibilities

• Accountable for one or more clinical programming trial activities of low complexity, scope and/or criticality.

• Performs review and input into, project requirements and documentation.

• Ensures latest standards are being utilized, current technologies are deployed.

• Review specifications for mapping internal data review model for fit for purpose reporting consumption and/or submission ready CDISC SDTM.

• Support internal data model for fit for purpose reporting consumption and/or submission ready CDISC SDTM packages for health authority submissions.

Provide programming support or oversight of quality review checks and reports for use by team members and consumers of data.

• May perform support 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.

• Collaborates effectively with team and cross-functional counterparts and vendors to achieve project goals.

• May contribute to departmental innovation and process improvement projects.

• Ensures continued compliance with required company and departmental training, time...