covance

Clin Data Processor I (BB-BE916)

Encontrado en: Neuvoo CR

Descripción:

Job Overview:

The role of the programmer analyst is to assist in the drug development process and Clinical Data Management Programming.

Education/Qualifications:

  • Bachelor's Degree in life science, computer science, engineering, business or related discipline
  • 1-3 years of experience in quality assurance and business analysis
  • Clinical research or data management experience preferred
  • Proficiency in converting complex technical and business requirements into an understandable test plan and test cases
  • Experience with clinical systems, such as CTMS, EDC, IVRS, Oracle Clinical or other related technology in the pharmaceutical/biotechnology industry preferred

    • Experience:

  • Responsible for developing, executing and coordinating the end-to-end User Acceptance Testing for Interactive Voice/Web Response Systems and Devices.Responsible for the quality review of UAT deliverables.Develop UAT documentation consisting of:: test cases, scenario based summaries and all other required documents.Work closely with team members for UAT execution and UAT error resolutionLead meetings with stakeholders to present UAT material.Ability to guide/instruct participants during the execution of User Acceptance Testing (UAT) and system integration testing.Collaborate with vendors and internal functions to develop scenarios for testing purposes.Execute UAT test scripts.Execute Quality Control related activities.Address and resolve UAT findings with vendor and core teams.Work within published study/system project timelines and attend meetings as necessary.Conform with GMP and GDP practices. Knowledge Skills Waterfall/Agile SDLC UAT processBusiness Analysis: End User RequirementsQuality AssuranceData management (Clinical data is plus)Sharing knowledge and active feedback in multicultural, multidisciplinary teamsSystems Development LifecycleCandidates should demonstrate technical expertise, attention to detail, and excellent documentation and communication skills.Experience creating, executing and documenting test plans and test cases is requiredExcellent time management and organization skills requiredMust have sound problem resolution, judgment, and decision making skillsDrug Development and Clinical Trials Processes is preferred

    • calendar_todayhace 12 horas

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    location_onSan José, Costa Rica

    work covance

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