Strategic Overview
Database Programmer at Alimentiv is defined by the responsibilities and candidate requirements in the employer's listing.
The published role emphasizes work such as Design, build, test, and maintain clinical study databases throughout the study lifecycle.
The role is listed for Canada, United States with a remote working arrangement, giving candidates the practical context needed to assess fit before applying.
Key information at a glance
About This Role
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!
Key Responsibilities & Objectives
- 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.
Required Qualifications & Candidate Blueprint
- A post-secondary certificate or diploma from a college, training institute, or equivalent institution. An equivalent combination of education and experience may be considered.
- 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.
Salary & Benefits
Published compensation: CAD 75,000 – 125,000 / yearly
- 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 Job Description
The following is the complete job description supplied by the source. We sanitize unsafe markup and remove external links, but do not shorten or rewrite the employer's source content.
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
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.
Key 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.
Skills & Qualifications
A post-secondary certificate or diploma from a college, training institute, or equivalent institution. An equivalent combination of education and experience may be considered.
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.
What We Offer
In addition, as an Alimentiv Employee, you’re also eligible for the following programs:
- 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!
Additional benefits may be available depending on the country of employment and are subject to local policies and eligibility.
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
To apply for this position, please submit your resume through the Alimentiv Careers Portal or via LinkedIn’s Easy Apply. Resumes must be submitted in English.
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. Requests can be directed to recruitment@alimentiv.com.
Compensation
Please note that the salary range may vary depending on the country in which the position is based.
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.
Additional Information
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.
Editor’s Market Perspective (Our Custom Analysis)
Why This Position Matters
This opening may suit candidates who can demonstrate experience relevant to the employer's published requirements. Its strongest career signal is the scope of the work itself — particularly Design, build, test, and maintain clinical study databases throughout the study lifecycle. — rather than a generic title alone.
Resume & Application Strategy
For the application, connect specific examples from your experience to the responsibilities and qualifications in the employer's description. Quantify outcomes from comparable work, and place the most relevant evidence near the top of the resume. When the employer explicitly names tools, platforms, leadership scope, or domain experience, use those source terms accurately and in context.
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