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Clin Data Processor I

Laboratory Corporation of America Holdings (Covance)

San José, Costa Rica

<h2≥Job Overview:</h2≥<p style="margin: 0px;"≥<span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"≥<span style="color: black;"≥The role of the programmer analyst is to assist in the </span≥<span style="color: black;"≥drug development process and Clinical Data Management Programming.</span≥</span≥</p≥<h2≥Education/Qualifications:</h2≥<ul≥<li style="margin-left: 25.85pt;"≥<span style="font-size: 10.0pt;"≥Bachelor's Degree in life science, computer science, engineering, business or related discipline</span≥</li≥<li style="margin-left: 25.85pt;"≥<span style="font-size: 10.0pt;"≥1-3 years of experience in quality assurance and business analysis</span≥</li≥<li style="margin-left: 25.85pt;"≥<span style="font-size: 10.0pt;"≥Clinical research or data management experience preferred</span≥</li≥<li style="margin-left: 25.85pt;"≥<span style="font-size: 10.0pt;"≥Proficiency in converting complex technical and business requirements into an understandable test plan and test cases</span≥</li≥<li style="margin-left: 25.85pt;"≥<span style="font-size: 10.0pt;"≥Experience with clinical systems, such as CTMS, EDC, IVRS, Oracle Clinical or other related technology in the pharmaceutical/biotechnology industry preferred</span≥</li≥</ul≥<p style="margin: 0px;"≥ </p≥<h2≥Experience:</h2≥<ul≥<li≥<ul style="margin-top: 0in;"≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Responsible for developing, executing and coordinating the end-to-end User Acceptance Testing for Interactive Voice/Web Response Systems and Devices.</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Responsible for the quality review of UAT deliverables.</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Develop UAT documentation consisting of:: test cases, scenario based summaries and all other required documents.</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Work closely with team members for UAT execution and UAT error resolution</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Lead meetings with stakeholders to present UAT material.</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Ability to guide/instruct participants during the execution of User Acceptance Testing (UAT) and system integration testing.</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Collaborate with vendors and internal functions to develop scenarios for testing purposes.</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Execute UAT test scripts.</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Execute Quality Control related activities.</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Address and resolve UAT findings with vendor and core teams.</span≥</li≥</ul≥<ul style="margin-top: 0in;"≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Work within published study/system project timelines and attend meetings as necessary.</span≥</li≥<li style="margin-left: .5in;"≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Conform with GMP and GDP practices.</span≥</li≥<li style="margin-left: .5in;"≥<strong≥<span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"≥Knowledge Skills</span≥</strong≥</li≥<li≥<span style="font-size: 10.0pt;"≥Waterfall/Agile SDLC UAT process</span≥</li≥<li≥<span style="font-size: 10.0pt;"≥Business Analysis: End User Requirements</span≥</li≥<li≥<span style="font-size: 10.0pt;"≥Quality Assurance</span≥</li≥<li≥<span style="font-size: 10.0pt;"≥Data management (Clinical data is plus)</span≥</li≥<li≥<span style="font-size: 10.0pt;"≥Sharing knowledge and active feedback in multicultural, multidisciplinary teamsSystems Development Lifecycle</span≥</li≥<li≥<span style="font-size: 10.0pt;"≥Candidates should demonstrate technical expertise, attention to detail, and excellent documentation and communication skills.</span≥</li≥<li≥<span style="font-size: 10.0pt;"≥Experience creating, executing and documenting test plans and test cases is required</span≥</li≥<li≥<span style="font-size: 10.0pt;"≥Excellent time management and organization skills required</span≥</li≥<li≥<span style="font-size: 10.0pt;"≥Must have sound problem resolution, judgment, and decision making skills</span≥</li≥<li≥<span style="font-size: 10.0pt;"≥Drug Development and Clinical Trials Processes is preferred</span≥</li≥<li style="margin-left: .5in;"≥ </li≥</ul≥</li≥</ul≥

Job posted: 2020-11-17

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