Junior Programmer

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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