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Ecoa Jobs in Indiana (NOW HIRING)

Superior Auto Inc

Chief Compliance Officer

Fort Wayne, IN · On-site

$150K - $200K/yr

Strong knowledge of federal regulations, including UDAAP, FCRA, FDCPA, TILA, ECOA, GLBA, and related consumer finance laws. * Experience managing regulatory examinations and advising executive ...

Rohrman Auto Group

Finance Manager

Lafayette, IN · On-site

$80 - $100/hr

Strong knowledge of federal and state compliance regulations (CFPB, TILA, ECOA, etc.). * Proficiency with DMS software (Reynolds & Reynolds, CDK, or equivalent). * Excellent communication and ...

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Ecoa information

What is an Ecoa?

The role of an Ecoa typically involves responsibilities related to environmental compliance, sustainability, or quality assurance, depending on the industry. These jobs often require monitoring and enforcing regulations, conducting assessments, and implementing policies to ensure environmental or operational standards are met. Specific duties may vary based on the organization and sector.

What does an Ecoa specialist do?

As an eCOA Specialist, your days often involve configuring and validating eCOA platforms for clinical studies, providing user training, troubleshooting technical issues, and ensuring accurate data capture in line with study protocols. You’ll work closely with clinical research teams, sponsors, and technology vendors to coordinate requirements and resolve issues promptly. Regular participation in team meetings and documentation of processes is also expected. This role offers a blend of technical, analytical, and collaborative tasks, making each day varied and engaging.

What are the key skills and qualifications needed to thrive in the Ecoa position?

To thrive as an eCOA (electronic Clinical Outcome Assessment) Specialist, you need a strong understanding of clinical research processes, data management, and regulatory guidelines, typically supported by a degree in life sciences or a related field. Familiarity with eCOA software platforms, electronic data capture (EDC) systems, and compliance standards like 21 CFR Part 11 is highly valued. Strong attention to detail, troubleshooting ability, and effective communication are essential soft skills for collaborating with sponsors, study teams, and vendors. These competencies ensure high-quality data collection, protocol compliance, and smooth execution of clinical trials.

What are popular job titles related to Ecoa jobs in Indiana?

For Ecoa jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Ecoa jobs in Indiana look for?

The top searched job categories for Ecoa jobs in Indiana are:

Ecoa jobs near you
Infographic showing various Ecoa job openings in Indiana as of August 2026, with employment types broken down into 76% Full Time, 22% Part Time, and 2% Contract. Highlights an 62% Physical, 6% Hybrid, and 32% Remote job distribution.

eCOA Programmer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Posted 25 days ago

Job description

Role Overview:
This role involves gathering and influencing eCOA design specifications to ensure successful trial implementation. The programmer will be responsible for developing and testing data collection systems and associated data repository mappings for clinical trials, ensuring accuracy and alignment with study objectives.
Key Responsibilities:
  • Gather and influence eCOA design specifications to enable successful trial implementation.
  • Program and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components.
  • Ensure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives.
  • Partner with Clinical Build Programmer to ensure complete data build for trial data collection needs.
  • Provide insights into study level deliverables (i.e., Data Management Plan, Project Plan, database, and observed datasets).
  • Support submission, inspection and regulatory response activities.
  • Lead cross Business Unit/Therapeutic Area projects or programs with high complexity.

Required Skills:
  • Hands-on experience as a programmer in eCOA (electronic Clinical Outcome Assessment) or eDC (electronic data capture), eSource or Direct Data Capture implementation.
  • Experience in the design of electronic CRF screens to capture Clinical data and build on required validations.
  • Understanding of Clinical Protocol and interpretation of Clinical terminologies to create or design specifications.
  • Familiarity with Clinical data tools, technologies, workflow for collecting patient data, testing and validation of systems.
  • Ability to analyze the impact and implement post-production changes to study design.
  • Proficiency in data analytics and visualizations.
  • Ability to articulate the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions.
  • Experience in deciding the technology platform (system/database) for data acquisition and aggregation.
  • Programming experience with HTML, CSS, JAVASCRIPT, Node.js, JSON, SpEL.
  • Experience with relational and non-relational database technologies utilizing SQL, Data Functions and Procedures (e.g., MongoDB).
  • Technical proficiency with HTML, Data Mapping, and understanding of database structures.
  • Experience handling GITLAB utilities.
  • Quick learner to new trends in technology.
  • Excellent leadership, communication (written and oral) and interpersonal skills.
  • Demonstrated leadership in a professional setting.
  • Demonstrated teamwork and collaboration in a professional setting.

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