| Sr Clinical Programmer (SAS supporting CDM) at Remote, Remote, USA |
| Email: [email protected] |
| From: Yashwant Singh, DMS Visions Inc [email protected] Reply to: [email protected] Hi professionals, Hope you all are doing well, Please find the job description given below and let me know your interest. Position: Sr Clinical Programmer (SAS supporting CDM) Location: 100% Remote Duration: 6+ months Job Description: The Senior Clinical Programmer will be responsible for the planning, implementation, and compliance of clinical trial data programming activities across multiple studies to produce high quality and timely deliverables for Data Management, and other internal stakeholders. The role will mainly focus on clinical data ingestion and transformation, including the generation of validation procedures/data quality edit checks, reports, listings, trackers, metrics, and dashboards. The position reports to the Director, Clinical Programming. Responsibilities Produce timely, high quality, and reliable clinical trial data listings, reports, and trackers for data cleaning, data review, adjudication, and study status tracking Provide input to the clinical data reporting requirement, data validation and data transfer specifications (if applicable) to ensure high quality deliverables Perform ingestion activities of multiple external data (Safety, ePRO, IRT, PK, etc.) Perform external data reconciliation and data quality check programming activities Perform ad hoc flexible and rapid programming arising from Data Management needs Collaborate with internal stakeholders and cross functional team members within Biometrics, Clinical Operations, and Clinical Development Contribute to the development and maintenance of a positive team-focused company culture Education, Experience, and Skills Bachelors degree or higher in a technical, scientific, or analytic discipline Minimum of 5 years experience supporting clinical and/or statistical programming activities in clinical research for all phases of clinical trials Solid knowledge of pharmaceutical and regulatory requirements, procedures, and policies, including GCP, ICH, 21 CFR part 11, and other related guidance documents Excellent SAS programming skills, with a thorough understanding of clinical data structures, Proc SQL, SAS macro and general database concepts Experience with EDC applications, preferably Rave EDC or Veeva CDMS Knowledge of advanced SQL concepts, JSON and Veeva CDB (a plus) Experience with varied business intelligence and analytic tools, Looker, R Shiny, Spotfire, Power BI, Tableau, and/or SAP BusinessObjects Knowledge of and experience with CDISC standards including CDASH Ability to critically analyze information, communicate outcomes, and prioritize actions Excellent computer skills; strong verbal and written communication skills Ability to work well in a cross-functional teams as a contributor Excellent interpersonal skills and demonstrated ability to establish and maintain professional and productive cross-functional working relationship If you are interested, please share your updated resume and suggest the best number & time to connect with you Thanks & Regards, Yashwant Singh | IT Recruiter | DMS Vision Inc. 4645 Avon Lane, Suite 210, Frisco, TX 75033 [email protected] | Desk- 972-645-5050 www.DMSVisions.com Keywords: business intelligence active directory rlang information technology |
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| Thu Dec 29 01:26:00 UTC 2022 |