Junior Programmer
Pubblicato il 25-08-2026 - Opis in Milano
We're looking for a proactive and detail-oriented junior
Programmer
to join our team and support the development, maintenance, and optimization of business and clinical database applications.
Responsibilities:
Develop, test, and maintain web-based business applications
Design and manage eCRF/clinical databases and related tools
Program online validation checks and troubleshoot system issues
Collaborate with cross-functional teams to gather user requirements and improve application performance
Support integrations between applications and ensure system functionality
Prepare technical documentation, reports, and software maintenance records
Ensure compliance with quality standards, KPIs, confidentiality, and project timelines
Requirements:
High School Diploma and/or Bachelor's Degree in Computer Science or related field
At least 1 year of experience in a similar role preferred
Good knowledge of English
Good knowledge of C# and SQL Server
Proficiency with Microsoft Office tools
Strong planning and organizational skills
Excellent communication and problem-solving abilities
Understanding of clinical data systems/eCRF environments is an advantage
What we offer:
Collaborative international environment
Opportunity to work on impactful clinical research projects
Professional growth and continuous learning
Dynamic role combining technology and healthcare innovation
Who we are:
OPIS is an International CRO with over 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects.
OPIS extensive expertise covers all phases of drug-related trials, taking care of the Sponsor beyond the therapeutic area, offering also accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training.
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