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Clinical Data Associate Jobs in Indiana (NOW HIRING)

Patient Access Rep II

Lafayette, IN · On-site

$16.75 - $21.25/hr

Enter patient billing and clinical data. * Identify co-payment procedures and fiscal procedures ... Preferred Associate's Degree * Required High School Diploma/GED Travel is required. Equal ...

Patient Access Rep II

Lafayette, IN · On-site

$16.50 - $21.25/hr

Enter patient billing and clinical data. * Identify co-payment procedures and fiscal procedures ... Preferred Associate's Degree * Required High School Diploma/GED TRAVEL IS REQUIRED: EQUAL ...

Patient Access Rep II

Lafayette, IN · On-site

$16.75 - $21.25/hr

Enter patient billing and clinical data. * Identify co-payment procedures and fiscal procedures ... Preferred Associate's Degree * Required High School Diploma/GED TRAVEL IS REQUIRED: EQUAL ...

Showing results 41-60

Clinical Data Associate information

See Indiana salary details

$13

$37

$82

How much do clinical data associate jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for clinical data associate in Indiana is $37.07, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $37.07 per hour, depending on experience, location, and employer.

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 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.

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 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.

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 are the most commonly searched types of Clinical Data jobs in Indiana?

The most popular types of Clinical Data jobs in Indiana are:

What cities in Indiana are hiring for Clinical Data Associate jobs?

Cities in Indiana with the most Clinical Data Associate job openings:

Infographic showing various Clinical Data Associate job openings in Indiana as of September 2026, with employment types broken down into 80% Full Time, and 20% Part Time. Highlights an 100% In-person job distribution, with an average salary of $77,096 per year, or $37.1 per hour.

Associate Director, Digital Knowledge Management & Data Strategy - SDnA

Indianapolis, IN • On-site

Eli Lilly and Company
Pharmaceutical Product Wholesalers • 10K+ employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago


Eli Lilly and Company rating

8.9

Company rating: 8.9 out of 10

Based on 64 frontline employees who took The Breakroom Quiz


Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Associate Director, Digital Knowledge Management & Data Strategy - Statistics, Data & Analytics
Position Overview
We are seeking an experienced Knowledge Management (KM) professional to lead data and knowledge initiatives within our global Statistics, Data & Analytics (SDnA) organization. This role will design and implement forward-thinking systems to collect, organize, and connect technical knowledge across functions, regions, and clinical development stages. It will also transform fragmented process documentation, procedures, and historical knowledge into a structured, searchable, dynamic knowledge repository with supporting systems and processes. Ultimately, this position will enhance efficiency, strengthen consistency, and reduce risk by making critical knowledge readily accessible to all employees within the organization.
Key Responsibilities
  • Strategy & Vision: Own the multi-year strategy for how SDnA captures, curates, and shares its collective knowledge. Design and implement modern, queryable, AI-navigable systems on enterprise platforms that support easy internal access and secure collaboration.
  • System Implementation & Optimization: Build or optimize a centralized knowledge system for statistical, data management, and analytics resources. Apply enterprise platforms and best practices to ensure that procedures, process maps, and supporting materials are searchable by global teams.
  • Ontology, Data & Process Mapping: Develop a domain ontology and process maps that reflect current SDnA workflows and information architecture. Honor study lifecycle sequence, functional ownership, and regulatory constraints. Apply the appropriate technical tools (e.g., coding, automation, low-code platforms, visualization software) to categorize knowledge assets, surface redundancies, map processes, and identify gaps.
  • Standards & Quality: Set the standards for how knowledge is created, tagged, versioned, and retired. Establish the taxonomy and content lifecycle model, and design automated quality checks that keep content clean, concise, accurate, and compliant as the organization changes.
  • Change Management & Training: Lead change management to drive adoption of new systems and practices. Develop training programs, user guides, and support resources. Champion a culture of knowledge-sharing through regular communication and leadership support.
  • Cross-Functional Collaboration: Work closely with statistics, data management, programming, regulatory, IT, and quality partners to align the system with business needs. Coordinate technical integrations and gather feedback from subject-matter experts to continuously improve the system.
  • Continuous Improvement & Impact: Monitor usage metrics and key performance indicators (e.g., most-accessed topics, search query success rates, content most in need of refresh, accuracy of content). Identify opportunities to improve efficiency and consistency, and maintain a vision for scaling knowledge management systems as the organization evolves.

Minimum Qualification Requirements
  • Experience: Demonstrated record of building scalable knowledge systems, drafting and implementing standards and procedures, and driving organizational adoption. Experience in knowledge management, information management, or data/analytics operations, with a focus on implementing KM systems.
  • Bachelor's degree. Advanced degree is a plus.
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization and/or visas for this role.

Other Information/Additional Preferences
  • Pharmaceutical or comparably regulated industry experience (roughly 5 years), including approximately 3 years in a KM-focused role.
  • Domain Knowledge: Understanding of the clinical data and analysis lifecycle and of the documents, workflows, and terminology used across them. This includes (but is not limited to) data standards, data management, statistical analysis and reporting, safety, and regulatory submission.
  • Technical Proficiency: Demonstrated ability to use technology for knowledge management. Hands-on proficiency with enterprise collaboration tools (e.g., SharePoint, document management systems) and scripting skills (Python preferred) for data analysis and automation. Familiarity with knowledge graphs, semantic retrieval, or AI-assisted approaches is a plus.
  • Standards & Governance Knowledge: Working knowledge of industry-standard information governance and data-handling practices. Experience developing standards for content management, version control, and access.
  • Leadership & Communication: Excellent project leadership with experience motivating change management. Superior communication and interpersonal skills to train users and build strong connections with employees, IT partners, and external collaborators. Skilled at influencing and championing new ideas, leading through ambiguity with sound judgment and transparent decision-making, and developing the capabilities of direct and indirect team members through structured coaching and honest feedback.
  • Industry Expertise: Prior experience leading knowledge management projects in a pharmaceutical, clinical research, or other regulated environment with global operations. Familiarity with emerging technologies, including AI, to enhance knowledge sharing.
  • Change Management Credentials: Formal training or certification in change management or process improvement (e.g., PROSCI, Six Sigma, Lean).
  • Cross-Functional Insight: Experience handling knowledge across multiple functions, regions, and time zones, coordinating with regional and global teams.
  • Strategic Vision: A forward-looking approach with the ability to anticipate future knowledge needs and scalability requirements. Experience building solutions that have measurably improved efficiency or reduced risk.

Long-Term Impact
Success in this role will be measured by the creation of a scalable, efficient, and well-governed knowledge sharing system for SDnA. The system this role builds will give SDnA employees fast, reliable access to accurate information, helping them navigate the study lifecycle and collaborate across functions and regions. Over time, this knowledge management system will reduce SDnA's operational risk by preserving institutional knowledge, resolving redundant efforts, and keeping content current and compliant as practices evolve. The ideal candidate will address immediate needs while laying a foundation for continuous improvement and innovation in the analytics function for years to come.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location.
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$115,500 - $169,400
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly

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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876