Database Programmers

Alimentiv; New Jersey; In loco; USD 85.000 - 120.000; Tempo pieno

Vantaggi offerti da questo lavoro

Education Reimbursement program

Monthly Cell Phone and Remote Work – (

Office setup allowance

Flexible Summer Hours

Alimentiv Trust after 1 year

Additional country-specific benefits

End-to-end GI clinical trial services

Medical imaging management and endosc?

Descrizione del lavoro

Alimentiv is a global CRO focused on GI therapies and clinical data management. The Database Programmer will design, develop, test, and maintain clinical study databases using Medidata Rave EDC, and will build custom C# functions to support EDC capabilities.

The role collaborates with project teams and sponsors to ensure data delivery, quality, and continuous improvement throughout the study lifecycle.

Competenze

• Post-secondary certificate or diploma required.
• 1–3 years of related database programming experience; 4–6 years preferred.
• Hands-on Medidata Rave EDC experience including development, configuration, and maintenance.
• Proficiency in C# programming for custom functions within Medidata Rave EDC.
• Experience developing and maintaining electronic Case Report Forms (eCRFs) and automated edit checks.
• Knowledge of clinical database programming processes including data transfers and uploads.
• Experience generating clinical data listings and project tracking reports.
• Strong troubleshooting and problem-solving abilities; independent work style.
• Excellent communication and collaboration with internal teams, sponsors, and stakeholders.
• Strong organizational skills with ability to manage competing priorities.

Mansioni

• Design, build, test, and maintain clinical study databases across the study lifecycle.
• Support deployment and ongoing adoption of Medidata Rave EDC across studies.
• Develop and test custom functions using C# for Medidata Rave EDC functionality.
• Create annotated eCRFs and program automated edit checks for data validation.
• Develop and test files for electronic data uploads, transfers, and integrations.
• Program and generate data listings and project tracking reports.
• Manage database access, change requests, and archive data and documentation.
• Troubleshoot and resolve database programming issues for internal teams and sponsors.
• Communicate progress, milestones, and issues to stakeholders.
• Contribute to process improvements in database programming.

Conoscenze

Attention to detail

Communication

Organizational skills

Troubleshooting

Formazione

Post-secondary certificate or diploma

Strumenti

Medidata Rave EDC

C# programming

Descrizione del lavoro

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.

The Database Programmer is responsible for the design, development, testing, maintenance, and archiving of clinical study databases throughout the study lifecycle. This role will play a key part in supporting the deployment, adoption, and ongoing development of Medidata Rave EDC as Alimentiv expands its Electronic Data Capture (EDC) capabilities.

The successful candidate will bring hands‑on experience with Medidata Rave EDC and C# programming to develop custom functions, support database configurations, and contribute to clinical database programming activities independently. Working closely with internal project teams and sponsors, this position will help ensure successful database delivery, technical support, and continuous improvement.

Responsibilities

• Design, build, test, and maintain clinical study databases throughout the study lifecycle.
• Support the deployment, implementation, and ongoing adoption of Medidata Rave EDC across clinical studies.
• Develop, program, and test custom functions using C# to support Medidata Rave EDC functionality.
• Create annotated electronic Case Report Forms (eCRFs) and program automated edit checks to support data validation.
• Develop and test files required for electronic data uploads, data transfers, and integrations.
• Program and generate clinical data listings and project tracking reports to support ongoing studies.
• Manage database access, process change request (CR) publishing requests, and archive electronic data and documentation upon study completion.
• Troubleshoot and resolve database programming issues, providing technical expertise and support to internal teams and sponsors.
• Communicate database setup progress, project milestones, and technical issues to internal and external stakeholders.
• Contribute to the development and improvement of database programming processes and departmental procedures.

Requirements

• A post-secondary certificate or diploma from a college, training institute, or equivalent institution.
• A minimum of 1–3 years of related database programming experience, with 4–6 years preferred.
• Hands‑on experience with Medidata Rave EDC, including clinical database development, configuration, and maintenance.
• Proficiency in C# programming, with the ability to independently develop, test, and troubleshoot custom functions within Medidata Rave EDC.
• Experience developing and maintaining electronic Case Report Forms (eCRFs) and automated edit checks.
• Knowledge of clinical database programming processes, including data transfers, electronic data uploads, and reporting.
• Experience generating clinical data listings and project tracking reports.
• Strong technical troubleshooting and problem‑solving skills, with the ability to independently address database programming challenges.
• Effective communication and collaboration skills, with the ability to work with internal project teams, sponsors, and external stakeholders.
• Strong organizational skills, attention to detail, and the ability to manage competing priorities and meet project milestones.

Benefits

• \\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.)
• Flexible Summer Hours Program from May – September
• Full‑time employees also become beneficiaries of the Alimentiv Trust after one year of employment, and permanent members after 5 years of employment
• Additional benefits may be available depending on the country of employment and are subject to local policies and eligibility.
• End‑to‑end GI clinical trial services, from protocol design through submission support
• Central medical imaging management and endoscopic reading

Performance-Based Incentive Program

At Alimentiv, we recognize and reward great performance. In addition to a competitive salary, eligible employees can participate in our Short-Term Incentive Plan (STIP) , which offers the opportunity to earn additional compensation based on individual contributions, team achievements, and company performance.

Equal Opportunity and Accessibility

Alimentiv is committed to building a diverse, inclusive and respectful workplace. We are an equal opportunity employer and consider all qualified applicants for employment without regard to race, colour, ethnicity, national origin, religion or belief, sex, gender identity or expression, sexual orientation, age, marital or family status, disability, or any other characteristic protected by applicable law.

Accommodations are available upon request for persons with disabilities throughout the recruitment and selection process.

\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.