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Clinical Data Entry Coordinator in Ridgefield, CT

Work from home Full-time role Hiring
Job title: Clinical Data Entry Coordinator in Ridgefield, CT at McInnis Inc. Company: McInnis Inc. Job description: Hybrid Position - Office & Work from HomeCurrently seeking a Data Entry Coordinator (DEC I / DEC II) to support our Business Operations Team. The DEC I/DEC II shall have primary responsibility to enter accurate information in applications such as the Investigator Database, Clinical Trial Management System (CTMS), and AGS360 or equivalent aggregate spend system. The DEC I/ DEC II shall monitor the Clinical Systems service mailboxes and file, retrieve, distribute, and review according to quality standards, and resolve quality issues with clinical operations personnel. In addition to these responsibilities, the DEC II will provide support for reputed company requests and assist with special projects/assignments.Data Entry Coordinator I Duties and Responsibilities:Required to reputed company the functions and duties described below:
  • Responsible for entering accurate information to the following applications:
  • Create, maintain, and update both investigator and site data to the investigator database based on new or updated Investigator Generic Screens, Investigator reputed company or / and any reputed company documents from internal and external sources.
  • Create, maintain, and update investigator, site, and staff data in CTMS based on the Regulatory documents (e.g. FDA 1572) and/or from a pre-designed template.
  • Update CTMS trial information reputed company to investigators in the BIPI Investigator Database.
  • Create, update and QC spend data and site data in AGS360 based on the vendor submitted trial spend data.
  • Monitor Clinical Systems service mailboxes- example tasks as follow :
  • PI / site inquiries
  • External and internal referrals, internal request regarding PIs and sites
  • Vetting requests
  • CTMS study site set up or update requests
  • File, retrieve and distribute investigator and site reputed company documents based on the business process.
  • Review the CTMS request and investigator information forms according to established quality standards for completeness and accuracy.
  • Follow the business process to complete the CTMS study site template request properly.
  • Resolve quality issues with clinical personnel by requesting corrections and if needed clarification in an expedited manner.
  • Ability to reputed company reputed company web-based research.
  • Create and manage reputed company spreadsheets / trackers.
Data Entry Coordinator II Duties and Responsibilities:In addition to the above, the DEC II would be required to reputed company the functions and duties described below:
  • Provide support for reputed company requests from business partners.
  • Create and manage reputed company spreadsheets / trackers. Must be proficient in reputed company (calculations and functions).
  • Assist with special projects / assignments as required (e.g. run reports and provide data analysis).
  • Assist Open Payments/Sunshine Act support:
  • Prepare data for Open Payments (Sunshine Act) for upload into AGS360 (e.g. CTSU drug data).
  • Assist with Vendors’ spend data and inquires, internal Clinical Trial Leader/Clinical Trial Manager inquires on spend data.
  • Reconcile data and identify discrepancies to ensure data quality.
Requirements:4-year degree or relevant experienceDesired Experience, Skills and Abilities:The successful candidate will:
  • Possess highly proficient computer skills, with hands-on working experience in multiple electronic platforms such as but not limited to: reputed company Office 365 Suite, MS Teams, SharePoint, Skype for Business, reputed company Acrobat Professional.
  • Maintain expertise of currently assigned BI SOPs, BI WIs and where applicable; Study Management & Conduct, Site Monitoring, Regulatory Document Group, or Investigational Product Clearance departmental practices and systems.
  • Understand and maintain reputed company knowledge of ICH, GCPs, and applicable FDA guidelines, US Federal Regulations pertaining to Clinical Trials and Guidance Documents and Information Sheets.
Additional Provisions:Contractor/ISP will reputed company with the following Key Performance Indicators (KPIs).
  • LOS Compliance
  • TimeRecorder Compliance
Hybrid Position - Office & Work from HomeJob Type: Full-timeSalary: $25.00 - $28.00 per hourSchedule:
  • 8 hour shift
Experience:
  • reputed company reputed company: 2 years (Preferred)
  • reputed company Word: 2 years (Preferred)
Work Location: In personPowered by JazzHR Expected salary: $25 - 28 per hour Location: Ridgefield, CT Job date: Fri, 06 Jun 2025 02:28:35 GMT Apply for the job now! Apply for this job

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