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Remote Data Cleaning Jobs in Kentucky (NOW HIRING)

RMS Energy

Technical Data Coordinator

Louisville, KY · Remote

Able to work independently in a remote environment * Willing to travel 25%+ to sites or industry ... Valid driver's license with a clean driving record Bonus Points for: * Associate's or Bachelor ...

Omnisend

We're data-driven. We test, we iterate, we improve. Gut feelings don't drive decisions - insights ... Remote work possibilities * Unlimited access to psychotherapy * A workstation budget * Personalized ...

All JobsData Cleaning JobsRemote Data Cleaning JobsRemote Data Cleaning Jobs in Kentucky

Remote Data Cleaning information

What is remote data cleaning?

Remote data cleaning is the process of identifying, correcting, or removing inaccurate, incomplete, or irrelevant data from datasets, all performed from a remote location rather than on-site. Professionals use specialized software and scripts to clean and organize data, ensuring its quality and consistency before analysis or use in business processes. This role is essential for organizations that rely on accurate data for decision-making and often involves tasks such as deduplication, error correction, and formatting standardization.

What are the key skills and qualifications needed to thrive as a remote data cleaning specialist, and why are they important?

To thrive as a Remote Data Cleaning Specialist, you need strong analytical skills, attention to detail, and experience with data management, often supported by a degree in a quantitative field. Proficiency with tools such as Microsoft Excel, SQL, Python (pandas), and data visualization platforms is commonly required. Excellent problem-solving abilities, time management, and clear communication help you collaborate effectively and maintain data integrity. These skills ensure that datasets are accurate, reliable, and ready for analysis, which is crucial for informed business decision-making.

What are some common challenges faced when working remotely as a data cleaning specialist, and how can they be addressed?

Remote data cleaning specialists often encounter challenges such as inconsistent data formats, limited access to original data sources, and communication gaps with team members. To address these, it's important to establish clear data standards, use collaborative tools for real-time updates, and schedule regular check-ins with stakeholders. Staying organized and documenting data cleaning processes also helps maintain quality and ensures team alignment, even when working from different locations.

What is the difference between Remote Data Cleaning vs Remote Data Entry?

AspectRemote Data CleaningRemote Data Entry
Primary FocusIdentifying and correcting errors in datasets, improving data qualityInputting and updating data into systems accurately
Skills RequiredData analysis, attention to detail, familiarity with data toolsTyping speed, accuracy, basic computer skills
Work EnvironmentData analysis platforms, spreadsheets, specialized cleaning toolsData management software, spreadsheets, databases
CertificationsData analysis, Excel, database managementBasic computer skills, typing certifications

Remote Data Cleaning involves reviewing and correcting datasets to ensure accuracy, often requiring analytical skills. Remote Data Entry focuses on accurately inputting data into systems. While both roles require attention to detail, data cleaning emphasizes quality control, whereas data entry emphasizes speed and accuracy in data input.

What are popular job titles related to Remote Data Cleaning jobs in Kentucky?

For Remote Data Cleaning jobs in Kentucky, the most frequently searched job titles are:

What job categories do people searching Remote Data Cleaning jobs in Kentucky look for?

The top searched job categories for Remote Data Cleaning jobs in Kentucky are:

What cities in Kentucky are hiring for Remote Data Cleaning jobs?

Cities in Kentucky with the most Remote Data Cleaning job openings:

Remote Data Cleaning jobs near you
Infographic showing various Remote Data Cleaning job openings in Kentucky as of August 2026, with employment types broken down into 82% Full Time, and 18% Part Time. Highlights an 100% Remote job distribution.

Senior Clinical Research Associate (level dependent on experience) - up to $10K sign-on bonus!

Covington, KY • On-site, Remote

CTI
See more jobs at CTIexternal

Full-time

Medical, PTO

Re-posted 8 days ago

Job description

Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) / Good Clinical Practice (GCP), and relevant regulations. Performs management of study site activities in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs).
What you'll do:
  • Serve as the main CTI contact for assigned study sites
  • Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in the Monitoring Plan while adhering to all applicable regulatory requirements, SOPs, and ICH GCP
  • Assist with study start-up activities, including feasibility, pre-study activities, and site selection
  • Collect, review, and track essential/regulatory documents
  • Participate in and complete all general and study-specific training as required
  • Participate in investigator, client, and project team meetings
  • Create and implement subject enrollment strategies for assigned study sites
  • Ensure proper storage, dispensation, and accountability of all Investigational Product (IP) and trial-related materials
  • Perform site management activities and provide ongoing updates of site status to the Clinical Project Manager
  • Conduct remote monitoring and complete the related activities in accordance with study study-specific Monitoring Plan

  • Utilize systems and reports to track subject status, subject case report form (CRF) retrieval/source document review (SDV), regulatory documents, and IP
  • Assist with project-specific activities as a member of the Project Team
  • May support in the development of CRFs and other study-related documents (subject worksheets, Monitoring Plan, etc.)
  • May support in the translation, customization, and review of Patient Information sheet and Informed Consent, protocol synopsis, and other study-applicable documents as per required procedures
  • Where applicable, provide support to the Regulatory Affairs Study Start-up Team in the preparation or
    revision of documentation for submission to Ethics Committee(s), Institutions' Ethics Committees, Regulatory Authorities, Competent Authorities or Institutions Administration Boards, and follow up on the evaluation process until approval is available. Provide regular updates to the Sponsor/ Client
  • Assist in preparing and coordinating Investigator and client meetings, and attend meetings as necessary
  • Liaise with Clinical Data Management for data cleaning activities
  • Identify site issues and implement corrective actions or escalate as appropriate
  • Manage ISF and TMF for all assigned study sites in accordance with SOPs or study-specific Monitoring Plans
  • Where applicable, support in contract negotiation with study sites, Investigator payments, and tracking of site payments

What You'll Bring:
  • At least 1 year of clinical trial monitoring experience or equivalent experience as determined by CTI Management and Human Resources
  • Bachelor's Degree or higher in an allied health field such as nursing, pharmacy, or health / natural science, or RN with an Associate's Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing experience, or equivalent experience as determined by CTI Management and Human Resources
  • Previous experience in conducting clinical research studies in a hospital setting, a pharmaceutical company, or a CRO
  • Demonstrated successful performance in a CRA position with a minimum of 1 year of on-site monitoring experience preferred

Why CTI?
  • Advance Your Career - We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
  • Join an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work-from-home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
  • Make a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important NoteIn light of the recent increase in hiring scams, if you're selected to move on to the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
Please Note
  • We will never communicate directly with you via Microsoft Teams Messaging or by text message
  • We will never ask for your bank account information at any point during the recruitment process

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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