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Clinical Trial Data Manager Jobs in Indiana (NOW HIRING)

Elanco

Project Lead Data Manager

Indianapolis, IN · Hybrid

$49.50 - $67/hr

Project Lead Data Manager As a Project Lead Data Manager, you will serve as a technical authority ... Direct experience with clinical trial data for regulatory authority submissions (e.g., FDA, EMA)

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All JobsClinical Trial Data JobsClinical Trial Data Manager JobsClinical Trial Data Manager Jobs in Indiana

Clinical Trial Data Manager information

See Indiana salary details

$27

$59

$91

How much do clinical trial data manager jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for clinical trial data manager in Indiana is $59.49, according to ZipRecruiter salary data. Most workers in this role earn between $48.27 and $67.02 per hour, depending on experience, location, and employer.

What is the difference between Clinical Trial Data Manager vs Clinical Research Coordinator?

AspectClinical Trial Data ManagerClinical Research Coordinator
Primary RoleManages and oversees clinical trial data collection, validation, and analysisCoordinates daily trial activities, patient recruitment, and site management
Required SkillsData management, database systems, regulatory compliancePatient interaction, study protocol adherence, site coordination
Work EnvironmentData management teams, clinical trial offices, CROsClinical sites, hospitals, research facilities
Common CertificationsCDMP, SAS certifications often preferredGCP certification often required

While both roles are essential in clinical trials, the Clinical Trial Data Manager focuses on data integrity and analysis, whereas the Clinical Research Coordinator handles site operations and patient interactions. Understanding these differences helps in choosing the right career path or job search focus within clinical research.

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For Clinical Trial Data Manager jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Data Manager jobs in Indiana look for?

The top searched job categories for Clinical Trial Data Manager jobs in Indiana are:

What cities in Indiana are hiring for Clinical Trial Data Manager jobs?

Cities in Indiana with the most Clinical Trial Data Manager job openings:

Clinical Trial Data Manager jobs near you
Infographic showing various Clinical Trial Data Manager job openings in Indiana as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $123,736 per year, or $59.5 per hour.

Clinical Research Data Entry Specialist

South Bend, IN

ObjectiveHealth
51 - 200 employees
Learn more about ObjectiveHealthexternal

Full-time

Re-posted 4 days ago

Job description

Description

Clinical Research Data Entry Specialist (Onsite)

The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC systems. This role supports clinical research studies by ensuring data quality, completeness, and compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. This position is ideal for a detail-oriented individual with data entry or administrative experience who is interested in building a career in clinical research. 


 ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to:

  • Increase patient access to research trials within our communities
  • Provide physicians with enhanced care options for current patients
  • Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the ultimate goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.


 Key Responsibilities:

  • Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. 
  • Review source documents and medical records to ensure complete and accurate transcription of participant data. 
  • Verify data for accuracy, completeness, and consistency prior to submission. 
  • Review, investigate, and resolve EDC data queries generated by sponsors, contract research organizations (CROs), or data management teams by comparing source documentation and collaborating with study personnel. 
  • Communicate with Clinical Research Coordinators, investigators, and other study staff to resolve missing, incomplete, or inconsistent data. 
  • Correct data discrepancies while maintaining appropriate documentation and audit trails within the EDC system. 
  • Ensure timely completion of data entry and query resolution to support study milestones and database lock. 
  • Maintain accurate study documentation related to data entry activities. 
  • Adhere to study protocols, sponsor requirements, Good Clinical Practice (GCP), HIPAA, and applicable regulatory guidelines. 
  • Assist with quality control reviews and support sponsor monitoring visits, audits, and regulatory inspections as needed. 
  • Maintain confidentiality of participant information and research data. 

Qualifications:

  • High school diploma or equivalent. 
  • 1+ years of data entry, administrative support, medical office, or related experience. 
  • Excellent attention to detail and data accuracy. 
  • Strong organizational and time management skills. 
  • Ability to manage multiple priorities and meet deadlines in a fast-paced environment. 
  • Strong written and verbal communication skills.

Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant 

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