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Junior Clinical Research Associate Jobs in Indiana

BioTalent

We are seeking an experienced Senior Clinical Research Associate (CRA) to independently manage and monitor clinical trial sites throughout the full study lifecycle, from start-up through close-out.

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Clinical Research Associate

Indianapolis, IN · On-site

Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

Becton, Dickinson and Company

The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations professional responsible for managing site monitoring and relationship activities across multiple clinical ...

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Junior Clinical Research Associate information

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$27.6K

$54.9K

$118.5K

How much do junior clinical research associate jobs pay per year?

As of Sep 5, 2026, the average yearly pay for junior clinical research associate in Indiana is $54,859.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,900.00 and $56,600.00 per year, depending on experience, location, and employer.

What is a junior clinical research associate?

A Junior Clinical Research Associate (Jr. CRA) assists in monitoring clinical trials to ensure they comply with regulatory guidelines, protocols, and Good Clinical Practice (GCP). They support senior CRAs by reviewing study documents, conducting site visits, and ensuring data accuracy. Jr. CRAs also help in training site staff, managing trial documentation, and assisting with ethics submissions. This entry-level role serves as a stepping stone to becoming a full Clinical Research Associate (CRA). Strong organizational skills and attention to detail are essential for success in this position.

What are some typical challenges a junior clinical research associate might face in their first year on the job?

Junior Clinical Research Associates often face challenges such as managing multiple study sites, learning complex regulatory requirements, and adapting to the fast-paced nature of clinical trials. You'll need to balance on-site monitoring visits with timely documentation and communication between sponsors, sites, and internal teams. Many new associates also find adjusting to frequent travel and strict adherence to protocols demanding at first. With support from more experienced colleagues and continuous training, most individuals quickly develop confidence and master these essential aspects of the role. Overcoming these early challenges not only builds strong foundations for future advancement but also helps ensure the success of clinical research projects.

What are the key skills and qualifications needed to thrive in the junior clinical research associate position, and why are they important?

To excel as a Junior Clinical Research Associate, you need a bachelor’s degree in life sciences or a related field, a basic understanding of clinical trial methodology, and familiarity with Good Clinical Practice (GCP) guidelines. Proficiency in using clinical trial management systems (CTMS), electronic data capture (EDC), and an understanding of regulatory documentation are often required. Strong attention to detail, organization, and effective communication skills help build relationships with study sites and ensure accurate reporting. These competencies are crucial for maintaining study integrity, regulatory compliance, and smooth collaboration within research teams.

What are popular job titles related to Junior Clinical Research Associate jobs in Indiana?

For Junior Clinical Research Associate jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Junior Clinical Research Associate jobs in Indiana look for?

The top searched job categories for Junior Clinical Research Associate jobs in Indiana are:

What cities in Indiana are hiring for Junior Clinical Research Associate jobs?

Cities in Indiana with the most Junior Clinical Research Associate job openings:

Junior Clinical Research Associate jobs near you
Infographic showing various Junior Clinical Research Associate job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $54,859 per year, or $26.4 per hour.

Senior Clinical Research Associate

BioTalent

On-site

Other

Posted 8 days ago

Job description


We are seeking an experienced Senior Clinical Research Associate (CRA) to independently manage and monitor clinical trial sites throughout the full study lifecycle, from start-up through close-out. This is a highly autonomous, field-based role requiring an experienced monitor who can take ownership of site activities with minimal supervision while ensuring the highest standards of compliance, data quality, and site performance.


Key Responsibilities

Independently conduct:

  • Site Qualification Visits (SQVs)
  • Site Initiation Visits (SIVs)
  • Interim Monitoring Visits (IMVs)
  • Close-Out Visits (COVs)
  • Serve as the primary point of contact for assigned clinical trial sites.
  • Ensure compliance with study protocols, ICH-GCP, FDA regulations, and applicable SOPs.
  • Perform source data verification, resolve site queries, and maintain data integrity and quality.
  • Manage Investigator Site Files (ISF) and support Trial Master File (TMF) documentation to maintain inspection readiness.
  • Conduct investigational product accountability and reconciliation activities.
  • Provide ongoing site training, support, and guidance throughout the study lifecycle.
  • Complete monitoring reports, follow-up letters, and visit documentation within required timelines.
  • Identify, escalate, and support resolution of site issues and compliance risks.


Requirements

  • Bachelor's degree in Life Sciences or a related scientific discipline.
  • Minimum 5 years of CRA monitoring experience within clinical research.
  • Proven experience independently managing sites across the full clinical trial lifecycle.
  • Strong knowledge of:
  • ICH-GCP
  • FDA regulations
  • Clinical trial operations
  • eCRF and electronic data capture systems
  • Demonstrated ability to manage multiple sites and priorities simultaneously.


Contract Details

  • Valid driver's licence required.
  • Up to 100% travel required, including air and ground travel.

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