ZipRecruiter

Log In

1

From Home Clinical Database Programmer Jobs in Kentucky

previous pagenext page

Showing results 21-40

All JobsClinical Database Programmer JobsFrom Home Clinical Database Programmer JobsFrom Home Clinical Database Programmer Jobs in Kentucky

From Home Clinical Database Programmer information

What is the difference between From Home Clinical Database Programmer vs On-Site Clinical Data Coordinator?

AspectFrom Home Clinical Database ProgrammerOn-Site Clinical Data Coordinator
CredentialsTypically requires a degree in health informatics, computer science, or related field; certifications like CDMP or SAS are commonUsually holds a degree in health sciences, nursing, or related field; certifications like CDMP may be preferred
Work EnvironmentRemote, home-based setting with flexible hoursOn-site at clinical trial sites or healthcare facilities
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinical research organizations, healthcare providers

While both roles involve managing clinical data, the From Home Clinical Database Programmer works remotely focusing on database development and programming, whereas the On-Site Clinical Data Coordinator handles data collection and management directly at clinical sites. The choice depends on your preference for remote work versus on-site responsibilities.

What are popular job titles related to From Home Clinical Database Programmer jobs in Kentucky?

For From Home Clinical Database Programmer jobs in Kentucky, the most frequently searched job titles are:

What job categories do people searching From Home Clinical Database Programmer jobs in Kentucky look for?

The top searched job categories for From Home Clinical Database Programmer jobs in Kentucky are:

What cities in Kentucky are hiring for From Home Clinical Database Programmer jobs?

Cities in Kentucky with the most From Home Clinical Database Programmer job openings:

From Home Clinical Database Programmer jobs near you
Infographic showing various From Home Clinical Database Programmer job openings in Kentucky as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 52% In-person, and 48% Remote job distribution.

Senior Biostatistician (Clinical Trial Experience Required)

CTI

Covington, KY • On-site, Remote

Full-time

Medical, PTO

Posted 14 days ago

Job description

What You'll Do:

  • Assist with the development and modification of department SOPs and work instructions
  • Assist with training new Biostatistics employees; mentor and assist junior level Biostatisticians
  • Develop study bids and changes in scope for Biostatistics tasks in response to prospective client’s request for proposals (RFPs)
  • Attend and present the Biostatistics study execution tasks at capabilities presentations.
  • As the lead Biostatistician on the studies to which you are assigned, perform, or oversee the following tasks:
    • Act as primary statistical contact for internal and external project team members
    • Manage projects to ensure statistics tasks are performed within the entire project timeline. Keep Biostatistics management aware of changes to project timelines
    • Proactively identify and communicate changes in scope to the clinical project manager and Biostatistics management
    • Review case report forms (CRFs) and completion instructions
    • Give input to database design and data edit considerations necessary to collect and clean data
    • Develop or review Interim Analysis Plans (IAPs) and Statistical Analysis Plans (SAPs) as needed per the protocol
    • Develop or review program specifications – SDTM and ADaM dataset specifications and mock tables, listings, and figures (TLFs) – needed to perform the analysis defined in the IAP/SAP
    • Perform the statistical analysis by independently programming derived datasets and TLFs and validate the developer’s corresponding programs per department SOPs
    • Review programming of other team members
    • Develop or review statistical methods and results sections of statistical reports, clinical study reports (CSRs), or publications
    • Plan and design clinical studies, including:
      • overall study design development
      • outcome / endpoint determination
      • power analysis / sample size estimation reports
      • randomization and blinding procedures development
      • statistical methods section development in the protocol
    • Develop or review Randomization Plans, and randomization programs or lists
  • Carry out all activities according to CTI SOPs and project-specific conventions within the framework of Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) guidelines
  • Rely on instructions and Biostatistics SOPs to ensure timely, standard, quality deliverables to customers
  • Maintain accurate records of all work performed and ensure all relevant statistics documents are filed in the eTMF per the project-specific eTMF Plan
  • Provide input to and participate in departmental meetings

    What You'll Bring:

    • At least 4 years of related biostatistics experience in either a pharmaceutical or CRO environment or other relatable statistical experience
    • Master’s degree in Biostatistics, Statistics, or related field
    • CDISC, SDTM, and ADaM dataset mapping experience
    • BLA/NDA Submission experience; regulatory representation (i.e., meeting preparation/attendance, follow-up with regulatory communication) preferred
    • Therapeutic experience in transplantation, autoimmune diseases, kidney and liver disease, oncology and rare disease preferred
    • Experience providing statistical consulting to internal/external clients preferred

    About CTI

    CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

    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 Note
    In light of recent increase in hiring scams, if you're selected to move onto 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 with you via Microsoft Teams or 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.

    Apply