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Clinical Study Associate Jobs in Indiana (NOW HIRING)

PurposeCare

Clinical Trainer

South Bend, IN · On-site

Evaluating service policies and recommending proposals for changes or study of problems which ... in the state.2. Bachelors or Associates Degree in Nursing from an accredited program.3. ...

Franciscan Health

Clinical Research Coordinator

Lafayette, IN · On-site

$23.25 - $31/hr

... study sponsor or sponsor's representative in a timely manner. QUALIFICATIONS * Associate degree ... Certified Clinical Research Professional (CCRP) within 1.5 years required * Certified Clinical ...

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Clinical Study Associate information

See Indiana salary details

$12

$30

$52

How much do clinical study associate jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for clinical study associate in Indiana is $30.01, according to ZipRecruiter salary data. Most workers in this role earn between $20.14 and $39.57 per hour, depending on experience, location, and employer.

What are Clinical Study Associates?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

What is the difference between Clinical Study Associate vs Clinical Research Coordinator?

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a Clinical Study Associate, and why are they important?

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
What are the most commonly searched types of Clinical Study jobs in Indiana? The most popular types of Clinical Study jobs in Indiana are:
What cities in Indiana are hiring for Clinical Study Associate jobs? Cities in Indiana with the most Clinical Study Associate job openings:
Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Indiana as of July 2026, with employment types broken down into 1% As Needed, 73% Full Time, 23% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $62,426 per year, or $30 per hour.
Clinical Research Coordinator

Clinical Research Coordinator

Franciscan Alliance

Indianapolis, IN

$23.25 - $30.75/hr

Full-time

Posted 2 days ago

Franciscan Health rating

6.8

Company rating: 6.8 out of 10

Based on 266 frontline employees who took The Breakroom Quiz

492nd of 890 rated healthcare providers

Job description

Franciscan Health Indianapolis Campus8111 S Emerson Ave Indianapolis, Indiana 46237

The Clinical Research Coordinator provides services related to the implementation and completion of clinical research protocols. This includes tasks such as obtaining informed consent for clinical trial participation, training other research team members, and completing all protocol-specified procedures.
WHO WE ARE
Franciscan Health is a leading healthcare organization dedicated to providing exceptional patient care and promoting health and wellness in our community. Our mission is to ensure that every patient receives the highest quality of care through innovation, compassion, and excellence. With 11 ministries and access points across Indiana, Franciscan Health is one of the largest Catholic health care systems in the Midwest. Franciscan Health takes pride in hiring coworkers who provide compassionate, comprehensive care for our patients and the communities we serve.

WHAT YOU CAN EXPECT

  • Schedule: Monday - Friday, 8am - 5pm (There is some flexibility with start/end time if needed)

  • Collaborate with Research Financial Analyst to ensure research billing is accurate.

  • Conduct a thorough and ongoing informed consent process and document appropriately.

  • Conduct clinical trials that involve human subjects according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines.

  • Create and complete valid source documentation per GCP requirements.

  • Document and maintain all research activities including patient visits.

  • Identify key elements of subject safety including, IRB oversight, study documentation, and event reporting.

  • Identify and explain key protocol elements to study subjects and perform study tasks as dictated by protocol.

  • Maintain research certification on a biannual or triannual basis, as appropriate.

  • Monitor adverse events and report serious events to the research sponsor according to written protocols and departmental standards.

  • Recruit and screen potential subjects for inclusion in clinical trials according to written protocols.

  • Respond to data queries issued by the study sponsor or sponsor's representative in a timely manner.

QUALIFICATIONS

  • Associate degree required (Health Administration, Business,Health Science, Nursing/Patient Care preferred)

  • Bachelor's Degree preferred

  • 3 years research experience required

  • IF RN, 3 years Nursing/Patient Care required

  • IATA training within 6 months of hire date required

  • Certified Clinical Research Professional (CCRP) within 1.5 years required

  • Certified Clinical Research Coordinator (CCRC) within 1.5 years required

TRAVEL IS REQUIRED:

Never or Rarely

EQUAL OPPORTUNITY EMPLOYER

It is the policy of Franciscan Alliance to provide equal employment to its employees and qualified applicants for employment as otherwise required by an applicable local, state or Federal law.

Franciscan Alliance reserves a Right of Conscience objection in the event local, state or Federal ordinances that violate its values and the free exercise of its religious rights.

Franciscan Alliance is committed to equal employment opportunity.

Franciscan provides eligible employees with comprehensive benefit offerings. Find an overview on thebenefit section of our career site, jobs.franciscanhealth.org.

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