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Clinical Operation Associate Jobs in Indiana (NOW HIRING)

BioTalent

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.

Trinityhealth

Clinical Supervisor RN

Mishawaka, IN · On-site

Will respond to daily clinical and operational issues when the Practice Manager is absent or unavailable. JOB SPECIFICATIONS AND CORE COMPETENCIES * Education: Associate degree in nursing required.

Trinity Health

Clinical Supervisor RN

Mishawaka, IN · On-site

Will respond to daily clinical and operational issues when the Practice Manager is absent or unavailable. JOB SPECIFICATIONS AND CORE COMPETENCIES * Education: Associate degree in nursing required.

Trinity Health

Clinical Supervisor RN

Mishawaka, IN · On-site

Will respond to daily clinical and operational issues when the Practice Manager is absent or unavailable. JOB SPECIFICATIONS AND CORE COMPETENCIES * Education: Associate degree in nursing required.

Ascension

Clinical Nurse Specialist

Evansville, IN · On-site

Clinical Operations Schedule: Full time, 40 hours a week, Day shift How you'll make an impact in ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

Ascension

Clinical Nurse Specialist

Evansville, IN · On-site

Clinical Operations Schedule: Full time, 40 hours a week, Day shift Life at Ascension: Where ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

Ascension

Clinical Nurse Specialist

Evansville, IN · On-site

Clinical Operations Schedule: Full time, 40 hours a week, Day shift Life at Ascension: Where ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

Ascension

Clinical Nurse Specialist

Evansville, IN · On-site

Clinical Operations Schedule: Full time, 40 hours a week, Day shift Life at Ascension: Where ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

Ascension

Clinical Nurse Specialist

Evansville, IN · On-site

$109K/yr

Clinical Operations Schedule: Full time, 40 hours a week, Day shift Life at Ascension: Where ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

Ascension

Clinical Nurse Specialist

Evansville, IN

Clinical Operations Schedule: Full time, 40 hours a week, Day shift Life at Ascension: Where ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

Ascension

Clinical Nurse Specialist

Evansville, IN · On-site

Clinical Operations Schedule: Full time, 40 hours a week, Day shift How you'll make an impact in ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

Ascension

Clinical Nurse Specialist

Evansville, IN · On-site

Clinical Operations Schedule: Full time, 40 hours a week, Day shift Life at Ascension: Where ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

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Clinical Operation Associate information

What is a clinical operation associate?

Clinical Operation Associates are professionals who support the planning, coordination, and execution of clinical trials within pharmaceutical, biotechnology, or clinical research organizations. They help ensure that clinical studies adhere to regulatory guidelines, timelines, and quality standards. Their responsibilities often include documentation management, assisting with trial site communications, tracking study progress, and supporting the clinical operations team with administrative tasks. Clinical Operation Associates play a vital role in the smooth running of clinical trials, contributing to the development of new medical treatments.

What are the key skills and qualifications needed to thrive as a clinical operation associate?

To thrive as a Clinical Operation Associate, you need a solid understanding of clinical trial processes, regulatory guidelines, and a relevant degree in life sciences or a health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC), and basic project management tools is typically required. Strong organizational skills, attention to detail, and effective communication are standout soft skills in this role. These capabilities ensure regulatory compliance, efficient trial execution, and seamless coordination among stakeholders in clinical research settings.

What are some common challenges clinical operation associates face when coordinating clinical trials, and how can they be managed?

Clinical Operation Associates often encounter challenges such as managing tight timelines, ensuring regulatory compliance, and coordinating communication among diverse stakeholders. Balancing multiple study sites and adapting to protocol amendments can also add complexity. Effective organization, proactive communication, and a strong understanding of clinical trial processes are key to overcoming these hurdles. Collaborating closely with site staff, clinical monitors, and project managers helps ensure that issues are identified early and addressed promptly, contributing to smoother trial operations.

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

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

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

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

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

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

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

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

Clinical Operation Associate jobs near you
Infographic showing various Clinical Operation Associate job openings in Indiana as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Senior Clinical Research Associate

BioTalent

On-site

Other

Posted 10 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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