Were 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 Bachelors 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.
This page is hosted by JazzHR and uses cookies for technical and analytical purposes. For details regarding the processing of your application data by OPIS please refer to our:
Were 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 applicationsDesign and manage eCRF/clinical databa...
Were 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 Bachelors 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.
This page is hosted by JazzHR and uses cookies for technical and analytical purposes. For details regarding the processing of your application data by OPIS please refer to our: