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Clinical System Designer IIICON plc is a world leading healthcare intelligence and clinical research organization.
We are proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical System Designer II to join ICON's Full-Service IOD Clinical Data Science team.Location: Mexico City (office-based with remote flexibility) - Colombia (home-based)ResponsibilitiesLead design and development of clinical systems, ensuring alignment with study protocols and operational needs.Consolidate and complete high level system requirements documents and manage their review.Copy and modify CRFs from standard libraries and other studies, providing support and review for re-use of library items.Develop Custom CRF screens, Edit Check, and Dynamic Check specification documents using prototyping methodologies.Perform quality control peer reviews of database related specifications and record comments appropriately.Lead eCRF and other specification review meetings.Utilize edit checks from the appropriate library and modify them to meet trial specific requirements, and program complex dynamic checks and discrepancy edit checks.Review all activity on an ongoing basis to identify out of scope tasks and bring them to the attention of the CSL.Support the CSL in negotiation of timelines and decision-making on the study.Assist in assessing impacts of post production database related changes and compile change management documentation for review by project team leads.Drive post production database changes and release into production.Travel approximately 10 percent domestically and/or internationally.Qualifications3+ years of experience in designing and implementing clinical systems within the clinical research industry.Expertise in data analysis and interpretation, with proficiency in clinical data management systems and software.Knowledge of at least one Clinical Data Management System (Medidata Rave, Veeva EDC, etc.).
Excellent functional knowledge of Clinical Data Management CRF design tools and the ability to plan and design CDMS components directly from interpretation of medium complexity clinical trial protocols.Excellent written and verbal communication skills.Equivalent combination of education, training, and relevant experience may be considered in place of the stated education and experience.All employees must read, write, and speak fluent English and the host country language.BenefitsVarious annual leave entitlements.A range of health insurance offerings to suit you and your family's needs.Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.General Employee Assistance Programme, LifeWorks, offering 24 hour access to a global network of independent specialized professionals.Life assurance.Adaptable country specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.Equal Employment Opportunity StatementAt ICON, inclusion and belonging are fundamental to our culture and values.
We are dedicated to providing an inclusive and accessible environment for all candidates.
ICON is committed to providing a workplace free of discrimination and harassment.
All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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📌 Clinical System Designer Ii (Bogotá)
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📍 Bogotá