Within this role you will coordinate and prioritize electronic laboratory data systems projects to maintain harmonization and electronic data integrity across IOPS sites and compliance with regulatory guidelines.
As a QC Electronic Data Management Analyst, a typical day might include, but is not limited to, the following: Working with cross-functional teams to define and prioritize electronic laboratory data systems projects and initiatives Harmonizing the use and management of electronic laboratory data systems across different laboratory environment Contributing to global projects aimed at harmonizing laboratory data systems Reviewing updates to regulatory guidelines for electronic data systems to ensure ongoing compliance Coordinating the needs of QC functional areas and establishing priorities for configurations of electronic data systems, such as implementing new specifications, designing system templates for new/revised test methods, and designing queries and reports Escalating issues like priority conflicts or project timeline delays to QC management Working with the IT LIMS and Lab System groups on projects such as defining User Requirement Specifications and executing test plans Providing support for additional computerized systems, such as LIMS (Laboratory Information Management System) Offering training and support to QC end-users Writing and revising Standard Operating Procedures (SOPs), User Requirement Specifications (URSs) and Functional Requirement Specifications (FRSs) with current formats Reviewing documents and ensure consistency with SOPs and current formats Ensuring data integrity for QC systems This role might be for you if: You are a passionate and innovative problem-solver You are team-oriented with strong communication skills You are an adaptable continuous learner You have experience with lab systems To be considered for this opportunity you should have a BS/BA in Life Sciences or related field and 2+ years of experience or equivalent combination of education and experience.
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