Job Overview :
Experience and ability to convert complex technical and business requirements into an understandable test plan and test cases
Preferred to have at least 2 years of experience with clinical systems, such as CTMS, EDC, IWRS, IVRS, Oracle Clinical or other related technology in the pharmaceutical / biotechnology industry
Experience creating, executing and documenting test plans and test cases
Hands on experience with IRT (IVR / IWRS / eCOA) systems
Clinical Data Management ProcessesSoftware Development Lifecycle (SDLC) and Software Testing Lifecycle (STLC)Candidates should demonstrate clinical and technical expertise, attention to detail, and excellent documentation and communication skills.
Must have sound problem resolution, judgment, and decision-making skills Ability to meet aggressive project timelines, while sustaining high performance, and high quality is essential.
Demonstrated ability to quickly learn new tools and technologies
Effectively prioritizes work, anticipates and proactively identifies problems, and develops and applies innovative solutions.
Education / Qualifications :
Bachelor’s Degree in life science, computer science, engineering, business or related discipline
1 - 3 years of experience in software validation in regulated environment, preferably pharmaceutical industry
Experience with Word, Excel and PowerPoint and be comfortable using these applications without support