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, business analysis, clinical research or data management
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
Data Management Processes
Systems Development Lifecycle
Candidates should demonstrate technical expertise, attention to detail, and excellent documentation and communication skills.
Experience creating, executing and documenting test plans and test cases
Excellent time management and organization skills required
Must have sound problem resolution, judgment, and decision making skills
Drug Development and Clinical Trials Processes is preferred
Work within published study / system project timelines and attend meetings as necessary.
Conform with GMP and GDP practices.
Responsible for developing, executing and coordinating the end-to-end Interactive Voice / Web Response System User Acceptance Testing.
Responsible for the quality review of UAT deliverables.
Develop UAT documentation consisting of : test cases, scenario based summaries and all other required documents.
Main contact with sponsor and all team members for UAT execution and UAT error resolution.
Lead 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 both Sponsor external 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.
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