Johnson & Johnson
Johnson & Johnson
Johnson & Johnson is a global healthcare company working across pharmaceuticals, medical devices, and consumer health. Its research and product development activities include medicines and therapies for oncology, immunology, neuroscience, and cardiopulmonary conditions, alongside MedTech solutions for cardiovascular care, orthopaedics, surgery, and vision. The company’s wider work also includes health and wellness education, large-scale manufacturing, investor activities, and global social-impact initiatives, creating opportunities across scientific, clinical, engineering, manufacturing, commercial, and corporate functions.

Senior R&D Digital Engineer, Clinical Trial Systems – Hybrid Belgium

Senior engineer supporting clinical trial management systems, site payments, and access provisioning for Johnson & Johnson. The role focuses on integrations, automation, analytics, compliance, and study-team enablement.

Description

  • Drive technology enhancements that improve CTM Solutions systems and processes and generate measurable value
  • Evaluate study-team requirements and turn them into effective system and process solutions
  • Support study configuration, ongoing maintenance, and successful system adoption across the study lifecycle
  • Resolve end-user requests submitted through service tickets and shared mailboxes with timely follow-through
  • Advance workflows through automation, analytics, and GenAI while meeting privacy, security, quality, compliance, and human-oversight standards
  • Manage releases, user acceptance testing, system enhancements, and integrations with IT, system owners, and suppliers
  • Diagnose complex system and process problems in collaboration with IT and vendors
  • Develop and provide training, operational guidance, and reference resources
  • Lead team meetings and participate in cross-functional initiatives
  • Assist with system and process audits, regulatory inspections, and corrective and preventive actions
  • Act as the connection between business users and key partners and stakeholders
  • Support customer enablement, metrics, user administration, integrations, continuous improvement, and change management

Requirements

  • A Bachelor’s degree is required, preferably in health, science, information technology, or a related discipline
  • At least five years of relevant clinical trial execution experience with a pharmaceutical company, medical device organization, or clinical research organization is required
  • Experience supporting IT systems and processes used in clinical development, reporting tools, Office 365 applications, and database administration
  • Working knowledge of drug development, including Good Clinical Practices and the FDA Code of Federal Regulations
  • Ability to collaborate with and influence stakeholders at every organizational level
  • Exceptional communication, business partnering, problem-solving, and prioritization abilities
  • A global business perspective
  • Willingness to travel up to 10% domestically or internationally
  • Project management or process improvement certification is preferred

Benefits

  • Annual bonus with a target determined by pay grade and location, based on individual and company performance
  • Sales commissions
  • Vacation days
  • At least 12 weeks of parental leave
  • Bereavement leave
  • Caregiver leave
  • Volunteer leave
  • Well-being reimbursement
  • Financial, physical, and mental health programs
  • Service anniversary and recognition awards
  • Insurance coverage for employees and, where applicable, eligible dependents
  • In the Netherlands, annual base pay includes an 8% holiday allowance