Senior EDC Programmer

Icon Clinical Research, Inc
Blue Bell, PA, United States
8 days ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
5 years minimum
Working hours
Regular working hours
Job source

Tech stack

Clinical Data Repository Computer Programming Data Validation Data Transmissions R (Programming Language) Python (Programming Language) Standard Sql SAS (Software) SQL Databases System Programming Data Management Veeva
+2 more
Custom Reports Programming Languages

Job description

  • Develop, validate, and maintain programming solutions for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials, using SAS, R, and/or Python
  • Develop and maintain programs required for handling external vendor data, using SAS, R, and/or SQL
  • Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process
  • Act as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team
  • Support knowledge sharing within the Programming group through presentations and preparation of training materials
  • Perform extracts of data from CDMS and creation of data transfer programs
  • Act as mentor and provide guidance and support to more junior programmer levels assigned to a project
  • Assist in the development and implementation of improvements to technical systems and processes within an SME role
  • Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies

Requirements

  • 5+ years of experience with EDC programming (Medidata Rave and/or Veeva) for data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials
  • Proficiency in one or more programming languages (R, Python, SAS and/or SQL)
  • Strong problem-solving and communication skills with the ability to work collaboratively in a fast-paced, cross-functional environment
  • Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results
  • Bachelor’s Degree in a relevant field

LI-TP1

Benefits & conditions

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

About the company

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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