Position: Entry level

Job type: Full-time

Loading ...

Job content

Job Title: Clinical Programmer II

Job 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
Supervisory Responsibilities: No supervisory responsibilities

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
    The company will not accept unsolicited resumes from third party vendors.

Loading ...
Loading ...

Deadline: 20-12-2024

Click to apply for free candidate

Apply

Loading ...

SIMILAR JOBS

Loading ...
Loading ...