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Clinical Research Data Manager Jobs in Indiana (NOW HIRING)

MediSphere Medical Research Center, LLC

Be Seen First

Clinical Research Assistant II

Evansville, IN · On-site

Position Summary The Clinical Research Assistant provides direct support to Clinical Research ... Documentation & Data Management * Accurately complete source documentation during participant ...

Bsu

Clinical Research Associate

Muncie, IN · On-site

$55K - $60K/yr

Contribute to data management, data analysis, interpretation of findings, and preparation of ... The Clinical Research Assistant must have experience in the field of Special Education. For ...

Actalent

Clinical Research Nurse

Indianapolis, IN · On-site

$28 - $37/hr

... This role manages a caseload of approximately 7-9 patients in active treatment, along with ... The coordinator will collaborate closely with nurses, physicians, regulatory and data teams, and ...

Parkview Health

Research Data Engineer

Fort Wayne, IN · On-site

$105K - $126K/yr

Experience working with EHR data, clinical trial datasets, or population health data is preferred ... Strong communication skills to manage and convey data warehouse plans to internal stakeholders.

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All JobsClinical Research Data JobsClinical Research Data Manager JobsClinical Research Data Manager Jobs in Indiana

Clinical Research Data Manager information

See Indiana salary details

$46.6K

$102.1K

$179.8K

How much do clinical research data manager jobs pay per year?

As of Aug 3, 2026, the average yearly pay for clinical research data manager in Indiana is $102,137.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,100.00 and $116,600.00 per year, depending on experience, location, and employer.

How to become a clinical research data manager?

To become a clinical research data manager, candidates typically need a bachelor's degree in health sciences, life sciences, or a related field, along with experience in clinical data management or research. Skills in database management, familiarity with electronic data capture (EDC) systems, and knowledge of regulatory requirements like GCP are essential. Certification such as the Society for Clinical Data Management (SCDM) CDMP can enhance job prospects.

How much does a Pfizer Clinical Data Manager make?

A Pfizer Clinical Data Manager typically earns between $80,000 and $120,000 annually, depending on experience, location, and level of responsibility. The role requires strong data management skills, familiarity with clinical trial software, and often a background in life sciences or healthcare. Salaries can vary based on the complexity of projects and the candidate's certifications.

What are some common challenges faced by Clinical Research Data Managers during multi-site trials?

Clinical Research Data Managers often encounter challenges coordinating data collection across multiple research sites, such as ensuring consistent data entry, handling discrepancies, and maintaining data quality standards. Effective communication with site staff and timely resolution of data queries are essential to minimize delays and errors. Utilizing robust electronic data capture (EDC) systems and standardized procedures helps, but proactive problem-solving and attention to detail remain crucial for success in this role.

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

AspectClinical Research Data ManagerClinical Research Coordinator
Primary RoleOversees data collection, management, and quality control of clinical trial data.Coordinates daily trial activities, patient recruitment, and site management.
Required SkillsData management, database systems, regulatory compliance.Patient interaction, study protocol adherence, site coordination.
Work EnvironmentData centers, clinical trial sites, research organizations.Clinical sites, hospitals, research facilities.
Common CertificationsCDMP, SAS, or related data management certifications.GCP certification, clinical trial training.

While both roles support clinical research, the Clinical Research Data Manager focuses on data integrity and management, whereas the Clinical Research Coordinator handles trial operations and participant coordination. Understanding these differences helps in choosing the right career path or job search focus.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, monitoring, or related roles. Entry-level roles in clinical research often include Clinical Trial Assistants or Coordinators, with CRAs generally needing a background in life sciences, good clinical practice (GCP) training, and sometimes certification such as CCRP or RAC.

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

To thrive as a Clinical Research Data Manager, you need a solid background in life sciences, data management principles, and experience with clinical trial processes, often backed by a relevant bachelor's degree. Proficiency in electronic data capture (EDC) systems, database management tools like SQL, and familiarity with regulatory standards such as GCP are essential. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration across research teams. These skills are crucial for maintaining high-quality, compliant data that support successful clinical trials and regulatory submissions.

What is a Clinical Research Data Manager?

A Clinical Research Data Manager is a professional responsible for collecting, organizing, and managing the data generated during clinical trials and research studies. They ensure that the data is accurate, complete, and complies with regulatory standards. Their work is crucial for the integrity of clinical research, as it allows researchers to draw valid conclusions from the study. Data managers work closely with clinical teams, statisticians, and regulatory bodies to maintain high-quality data throughout the research process.

What does a data manager do in clinical trials?

A clinical research data manager is responsible for collecting, organizing, and maintaining data from clinical trials to ensure accuracy, completeness, and compliance with regulatory standards. They often use data management tools like electronic data capture (EDC) systems and collaborate with research teams to support data quality and integrity throughout the study. Strong attention to detail and knowledge of Good Clinical Practice (GCP) are essential for this role.
What are the most commonly searched types of Clinical Research Data jobs in Indiana? The most popular types of Clinical Research Data jobs in Indiana are:
What are popular job titles related to Clinical Research Data Manager jobs in Indiana? For Clinical Research Data Manager jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Clinical Research Data Manager jobs in Indiana look for? The top searched job categories for Clinical Research Data Manager jobs in Indiana are:
What cities in Indiana are hiring for Clinical Research Data Manager jobs? Cities in Indiana with the most Clinical Research Data Manager job openings:
Clinical Research Data Manager jobs near you
Infographic showing various Clinical Research Data Manager job openings in Indiana as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $102,137 per year, or $49.1 per hour.

Clinical Research Data Entry Specialist

ObjectiveHealth

South Bend, IN

Other

Posted 10 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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