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Open nowPosted 5 days ago

Clinical Database Programmer

Alimentiv35 open roles

Where
Dublin
Work mode
Remote
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Your applicationOpen nowClinical Database ProgrammerAlimentiv · Dublin

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The clock on this job

Early applications get read.

13.1% of postings close within 7 days. Measured by our own scanner across the market. Alimentiv postings stay open a median of 11 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.7%3 days
  3. 13.1%7 days
  4. 21.1%14 days
  5. 35.7%30 days
  6. 58.7%60 days
This job: posted 5 days ago

Alimentiv median: 11 days open

The posting

Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development. We operate as a private, profit-with-purpose company, channeling our commercial success back into scientific research, technology, and our people. With approximately 700 people across multiple countries and three service lines, we are growing deliberately, and the capability of our leaders and our organization is central to how we get there.

If you want to do meaningful work, build something real, and invest back in research that changes lives — we want to meet you!

Job Overview

As a Clinical Database Programmer (internally referred to as Database Programmer), you will support the development, testing and maintenance of Electronic Data Capture (EDC) systems used in clinical trials.

Working within a collaborative and innovative technical team, you will be involved in building clinical studies, developing electronic Case Report Forms (eCRFs), configuring edit checks and supporting data integrations, primarily using Medidata Rave.

You will also have opportunities to contribute to new initiatives, explore AI-driven solutions and support continuous improvements in study development and operational efficiency.

Key Responsibilities

  • Design, build, test and maintain clinical study databases within EDC systems.
  • Develop and configure eCRFs, edit checks and study-specific database requirements.
  • Support clinical data transfers, integrations and database validation activities.
  • Troubleshoot technical issues and provide ongoing EDC study support.
  • Collaborate with Data Management, project teams and sponsors to ensure successful study delivery.
  • Contribute to process improvements, automation and innovative solutions, including the use of AI.
  • Support multiple clinical studies and progressively take ownership of study builds.
  • Ensure database documentation, quality standards and study timelines are maintained.

Requirements & Qualifications

  • Degree or diploma in Computer Science, Information Technology or a related field, or equivalent relevant experience.
  • Previous experience in clinical database development, EDC programming or clinical study builds.
  • Previous experience within a CRO or pharmaceutical environment.
  • Knowledge of eCRFs, edit checks, database testing and clinical data management processes.
  • Understanding of programming principles, logic and database development.
  • Strong analytical, problem-solving and organisational skills.
  • Experience supporting EDC integrations, technical initiatives or bid defence activities.
  • Proactive team player with excellent communication skills and a continuous improvement mindset.

Nice to Have

  • Hands-on experience with Medidata Rave, including study builds and configuration.
  • Knowledge of C# programming and development of custom functions within Medidata Rave.
  • Experience with AI tools, automation or AI-assisted programming to improve study development and efficiency.

What We Offer

  • Education Reimbursement program for full-time employees
  • Monthly Cell Phone and Remote Work Allowance (dependent on role eligibility)
  • One time office setup allowance (can be used to purchase a scanner/printer, extra monitor, office furniture, etc.)
  • Working while visiting program – up to 4 weeks per year!
  • Flexible Summer Hours Program from May – September
  • Employee referral incentive – we know great people know other great people, and we think that warrants recognition!
  • Full-time employees also become beneficiaries of the Alimentiv Trust after one year of employment, and permanent members after 5 years of employment
  • Optional formal mentorship program (Alimentorship); country/region annual social events in person; leadership development programs for people leaders in accordance with your seniority; social committee and several other optional initiatives designed to support you in feeling like part of the Alimentiv team!

Our Services

  • End-to-end GI clinical trial services, from protocol design through submission support
  • Central medical imaging management and endoscopic reading
  • Precision medicine and biomarker solutions
  • Real-world evidence and clinical consulting
  • Histopathology and lab services through AcelaBio

How to Apply

Equal Opportunity and Accessibility

Stay Alert to Recruitment Scams

Alimentiv is aware of a continued increase in phishing scams, which use various methods of attack via email, text, voice and social media, including individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process.

Official communication will only come from company email addresses containing "@alimentiv.com". If you are contacted about an open job at Alimentiv, please verify the domain of the sender's email address and confirm that you are being asked to apply on this website. If something doesn't feel right, we encourage you to verify before responding. If you believe you have been the victim of a phishing scam, please contact your local government cyber authority to report it.

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