***Sr. Clinical Programmer Analyst******100% Remote******Upto $50/hr on W2******12 Months contract (Possible extension/conversion) Responsibilities:Senior Rave Programmer Responsible for designing the eCRF in leading EDC systems in Rave Technical expertise, technical writing ability, and proficiency in Systems Development LifeCycle (SDLC) principles.Provide technical support and troubleshooting for Rave study development as well as site management and user access within supported RAVE modulesServe as system administrator to grant user access using iMedidata Cloud Administration for RAVE EDC, Coder, Lab Admin, RTSM and MMI (Imaging) provide Oversight, guidance, and design of study build activities on Rave URL.Create Advanced Analytics dashboardsInsights into creating actionable dashboards and deep understanding and knowledge of good interpretation of clinical dataResponsible for the preparation and /or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistencyResponsible for conducting Quality Control of study design for assigned projects and participate in the validation of EDC studiesResponsible for the creation and maintenance of library objects within the Global LibrariesResponsible for ensuring compliance of standard objects usage throughout the businessResponsible for the management of standard objects within the Global LibrariesPerform all activities related to specification development for study build and design of databases according to Standard proceduresResponsible for the review and approval of derivations and edit checks requested by the project teamsParticipate in the development of global, harmonized SOPs and specific quality work instruction for technical service group activitiesComplete work according to clients SOPs, Work Instructions and project specific guidelines in accordance with Good Clinical Practice Qualifications:Minimum 10 years of relevant work experience to include data management and/or database programming and spec Design activities including 10 years in Medidata RAVEStrong Programming skill setKnowledge of Python, building dashboardsKnowledge of API programmingDemonstrate excellent problem-solving skills, a proactive approach and the ability to make sound decisionsDemonstrated skill in leading teams, by example and mentoring staffExcellent oral and written communication and presentation skillsKnowledge of clinical trial process and data management, CRF/eCRF Design, CDISC. Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companiesDemonstrated ability to work in a team environmentDemonstrated ability to handle multiple competing prioritiesProven interpersonal skills #J-18808-Ljbffr
Teamwork Prioritization Troubleshooting data-management Establishing interpersonal relationships Problem-solving Technical Writing Communication Mentoring System administration Analytics Standard Operating Procedure (SOP) Presentation skills Leadership Quality control (QC) Technical Support