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Clinical Data Associate Jobs in Dry Ridge, KY (NOW HIRING)

SEB Interventionist

KY · On-site

$18.75 - $25/hr

Licensed Professional Clinical Counselor; or Licensed Professional Clinical Counselor Associate ... data * Communicate regularly with school staff and parents on student needs, goals, and ...

Amp Up Your Career We are seeking a Front Office Associate who is ready to join an organization ... In this role, you will manage the customer intake process, support clinical operations, and drive ...

Amp Up Your Career We are seeking a Front Office Associate who is ready to join an organization ... In this role, you will manage the customer intake process, support clinical operations, and drive ...

Amp Up Your Career We are seeking a Front Office Associate who is ready to join an organization ... In this role, you will manage the customer intake process, support clinical operations, and drive ...

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Clinical Data Associate information

See Dry Ridge, KY salary details

$12

$35

$80

How much do clinical data associate jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for clinical data associate in Dry Ridge, KY is $35.95, according to ZipRecruiter salary data. Most workers in this role earn between $27.07 and $35.96 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Data Associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

Which is better, CDM or SAS?

For a Clinical Data Associate, SAS is a widely used software for data analysis and reporting in clinical trials, while CDM (Clinical Data Management) refers to the overall process of collecting, cleaning, and managing clinical data, often using various tools including SAS. SAS skills are highly valued in the role, but understanding the broader CDM process is also important for effective data handling and compliance.

What's next after CRC?

After working as a Clinical Research Coordinator (CRC), professionals often advance to roles such as Clinical Data Associate, Clinical Trial Manager, or Regulatory Affairs Specialist. Gaining experience, certifications like CCRP, and developing skills in data management and regulatory compliance can facilitate career progression in clinical research.

What are the key skills and qualifications needed to thrive as a Clinical Data Associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a Clinical Data Associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What is the role of a clinical data associate?

A clinical data associate is responsible for collecting, managing, and ensuring the accuracy of data from clinical trials. They review data for completeness, resolve discrepancies, and use database tools to support data integrity and regulatory compliance throughout the trial process.

What Does a Clinical Data Associate Do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

Do you need a degree to be a CRC?

A Clinical Data Associate (CDA) typically does not require a specific degree, but a background in life sciences, healthcare, or related fields is often preferred. Many employers value relevant certifications and experience with clinical data management tools. Educational requirements can vary by employer and job level.

Is CRA an entry level job?

A Clinical Data Associate (CDA) role is typically considered an entry-level position in clinical research, often requiring a bachelor's degree in a related field and some familiarity with data management tools. However, a Clinical Research Associate (CRA) role usually requires more experience and is considered a mid- to senior-level position, involving site monitoring and regulatory compliance. Entry-level roles may serve as a stepping stone toward CRA positions with additional experience and certifications.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What cities near Dry Ridge, KY are hiring for Clinical Data Associate jobs? Cities near Dry Ridge, KY with the most Clinical Data Associate job openings:
Infographic showing various Clinical Data Associate job openings in Dry Ridge, KY as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $74,774 per year, or $35.9 per hour.
Specialist Supply Chain Mgmt

Specialist Supply Chain Mgmt

St. Elizabeth Healthcare

Erlanger, KY • On-site

Full-time

Medical, Retirement, PTO

Posted 4 days ago


St. Elizabeth Healthcare rating

6.5

Company rating: 6.5 out of 10

Based on 125 frontline employees who took The Breakroom Quiz

607th of 886 rated healthcare providers


Job description

Engage with us for your next career opportunity. Right Here.

Job Type:

Regular

Scheduled Hours:

40

đź’™ Why You'll Love Working with St. Elizabeth Healthcare

At St. Elizabeth Healthcare, every role supports our mission to provide comprehensive and compassionate care to the communities we serve. For more than 160 years, St. Elizabeth Healthcare has been a trusted provider of quality care across Kentucky, Indiana, and Ohio. We're guided by our mission to improve the health of the communities we serve and by our values of excellence, integrity, compassion, and teamwork. Our associates are the heart of everything we do.

🌟 Benefits That Support You

We invest in you - personally and professionally.

Enjoy:

- Competitive pay and comprehensive health coverage within the first 30 days.

- Generous paid time off and flexible work schedules

- Retirement savings with employer match

- Tuition reimbursement and professional development opportunities

- Wellness, mental health, and recognition programs

- Career advancement through mentorship and internal mobility

Job Summary:

Responsible for creating and maintaining spreadsheets, trackers for savings initiatives, rounding experiences, clinical trackers and project plans. Responsible for auditing and reviewing expired contracts, policies and procedures and responsible for maintaining weekly huddle board data. Reviewing current and new office/department related policies and procedures, coordination of general office functions and associates. Responsible for providing daily administrative support to System Director, Director of Procurement, Director of Operations and Director of Strategic Sourcing. Responsible for power point presentations, ordering office supplies, calendar management and meeting coordination. Research, review and manage all department events for fund raising, team building, etc.
Demonstrates respect, dignity, kindness and empathy in each encounter with all patients, families, visitors, vendors, and other associates regardless of cultural background.

Job Description:

Data Management/Coordination

  • Responsible for creating presentations, ad hoc reports and data collection/analysis.
  • Responsible for intake processing and data gathering for Director of Strategic Sourcing for New Product Requests for Periop, Imaging, General Nursing, and Administration, prepare Value Analysis Team Presentations, savings tracking, etc.
  • Assist Sr. Financial Analyst with monitoring of department budget, reports, research, credit card reconciliations, and year end accrual information for AP
  • Process invoices, expense reports, Match Exceptions/PO receipts, etc.
  • Assist Contract Coordinator with, monitoring, and tracking of Supply Chain Management Compliance 360 contracts/amendments and data accuracy for data requests from The Joint Commission, state surveys, finance, state & Federal reports, National Association reports, and hospital legal department.
  • Manage and monitor department Policies/Procedures regularly, work with team to revise/update according to schedule.
  • Responsible for regular updating/tracking of Premier Ascend program compliance/action plans.
  • Serve as the Administrator for the SCM Intranet web page updating information such as contact information/org charts, and important bulletins.
  • Responsible for regular updating/tracking of Local Contracts for Contracting Coordinator for action plans/status updates.

Office Coordination

  • Responsible for providing administrative support and coordination to facilitate overall office workflow for System Director, Directors, and Managers.
  • Manage special projects, documentation and recordkeeping including preparing presentations, creating process flows, correspondence, memos, reports, audits, policies/procedures, updating job descriptions, etc., while always maintaining strict confidentiality.
  • Coordinate internal and external meetings including room and equipment needs, catering, agenda, meeting minutes, and correspondence to participants
  • Responsible for creating, updating, and implementing department orientation process for new SCM associates, management of interview for prospective and hired associates including establishing interview panels, calculating assessment scores, establishing/editing department onboarding process (includes orientation schedules) for prospective and hired associates and coordinating/providing training as needed.
  • Responsible for management of monthly "Intro to SCM New Leader Orientation" for associates outside of SCM department.
  • Exhibit problem solving skills to immediately address needs of leadership, associates, or vendors in a timely, effective, and accurate manner while demonstrating ICARE Values.
  • Coordinate and implement department/team activities such as annual team building, community volunteerism, holiday celebrations, retirement teas, etc.
  • Manage Announcements and Improvement Opportunities sections of the weekly department Huddle Board.
  • Assist with non-clinical initiatives and serve as backup support when resources within the department are strained.
  • Provide daily administrative support and manage calendars for System Director, Director of Procurement, Director of Operations and Director of Strategic Sourcing.

Administrative Coordination

  • Responsible for providing daily general office support for the department.
  • Review/edit associate timecards and System Access Requests (SARS) as appropriate, compile and update periodic reports.
  • Implement office related policies & procedures.
  • Facilitate the approval flow of New Vendor Request forms.
  • Serve as liaison with office staff and vendors/IT department to address system/software/hardware issues.
  • Order and restock break room and office supplies, sort mail, greet visitors.
  • Coordinate travel arrangements/off-site meetings.
  • Welcome visitors and identify the purpose of their visit before directing them to the appropriate staff,
  • Perform other duties as requested.

Education, Credentials, Licenses:

  • High School Diploma
  • 1 year of college/business classes/trade education with emphasis in office management.

Specialized Knowledge:

  • Knowledge of electronic databases must be able to type 60 WPM, proficient in excel and PowerPoint Presentations Microsoft Outlook/TEAMS

Kind and Length of Experience:

  • Minimum of 4 years' experience in a fast pace office environment
  • Must be able to multi-task and have the ability to prioritize different projects at the same time.

FLSA Status:

Non-Exempt

Right Career. Right Here. If you're looking for the right careers in healthcare, the right place to be is at St. Elizabeth. Join us, and you'll take pride in the level of care we offer our community.


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