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Clinical Programmer II
View: 182
Update day: 05-11-2024
Location: Keelung City
Category: R & D IT - Software
Industry: Research Services Biotechnology Research Pharmaceutical Manufacturing
Position: Entry level
Job type: Full-time
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Job content
Job Title: Clinical Programmer IIJob Location: LOCATION
Job Overview
The Clinical Programmer II (CP-II) supports clinical programming services. The CP-II creates, deploys, and maintains clinical databases and provides support to the study team as needed. The CP-II provides technical and functional expertise in EDC and IRT systems, and where appropriate, mentors and supports other staff and peers on clinical databases.
Job Duties And Responsibilities
- Design, manage, and maintain the clinical databases in keeping with the protocols and amendments, standard operating procedures (SOPs), good clinical practices (GCP), and other regulatory requirements.
- Review system specifications and Data Validation Plan (DVP) and perform programming and configuration activities for assigned projects
- Participate in release to production activities
- Deliver milestones in a timely fashion for assigned projects
- Communicate progress on milestones to management and other stakeholders
- Review study risks and mitigation plans related to clinical databases and provide inputs to management and study teams
- Serve as the subject matter expert on data collection strategy and system functionality
- Provide ongoing technical support to end-users in assigned projects
- Participate in process improvements and the implementation of new systems and tools, as applicable
- Effectively present to groups and conduct or participate in meetings, as applicable
- Support less experienced Clinical Programmers
- Perform other tasks that are related to clinical programming, data analysis and reporting as assigned
Job Requirements
- Education
- Scientific, Informatics, Mathematics or Medical Documentation degree
- Experience
- At least 2 years of experience in design and deployment of clinical databases
- C#, SQL, and/or custom function programming (preferred)
- Medidata and/or Medrio configuration (preferred)
- Knowledge of pharmaceutical industry and data standards (preferred)
- Regular use of MS-Office, revision control system (e.g. Subversion), and issue tracking software (e.g. JIRA)
- Skills/Competencies
- Analysis: gathers and synthesizes complex information and requirements.
- Problem solving: identifies and/or resolves problems in a timely manner.
- Communication: speaks clearly and persuasively in positive or negative situations; good command of the English language
- Time management: prioritizes and plans work activities, uses time efficiently and develops realistic action plans.
- Quality management: promotes quality improvements and demonstrates accuracy and thoroughness.
- Judgment: exhibits sound judgment and makes timely decisions.
- Safety and security: actively promotes and personally observes safety and security procedures, and uses equipment and materials properly.
- Capabilities
- Ability to work remotely as applicable
- High level of working time flexibility to adjust to project flows
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Deadline: 20-12-2024
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