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Clinical Study Associate Jobs in Indiana (NOW HIRING)

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Clinical Study Associate information

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$52

How much do clinical study associate jobs pay per hour?

As of Jul 26, 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 Development Trial Lead Assoc Dir

Globalchannelmanagement

Indianapolis, IN

Full-time

Posted 7 days ago

Job description

Clinical Development Trial Lead Assoc Dir requires:

  • Stamford, CT or Indianapolis, IN
  • 5+ years clinical research experience or relevant experience in a scientific or health-related field
  • Experience with oncology (early & late phase clinical trials)
  • Applied knowledge of project management methodology, processes and tools
  • Demonstrated ability to lead and work effectively cross-culturally with global colleagues and with TPOs
  • Be recognized as a leader with demonstrated ability to coach others in process expertise.
  • Embrace strategic organizational changes and lead others effectively through these, exhibiting flexibility to adjust quickly and effectively to frequent change and altered priorities
  • Ability to influence without authority
  • Previous experience working in cross-functional teams/ projects and/or ability to establish and maintain relationships Effective and influential communication, self-management, and organizational skills
  • Demonstrated ability to handle complex situations through problem-solving, critical thinking and navigating ambiguity Other Information/Additional
  • Minimum of 5 years clinical trial experience with a strong working knowledge of the clinical research process
  • Prior clinical trial site-level or affiliate experience
  • Prior experience with local/country regional requirements
  • Strong analytical skills Proficiency in use of project management tools and techniques (e.g., Critical Chain, Veeva, MS Project, MS Excel, MS PowerPoint, PowerBI)
  • Need to travel periodically to scientific/regional meetings
  • Associate Director, Clinical Development Trial Lead (CDTL)
  • Clinical Trial Process Leadership and Expertise
  • Leverage and demonstrate broad understanding of therapeutic, clinical drug development, and process expertise in order to influence study design and program-level decisions considering regional needs.
  • Recognize inter-relatedness of cross-functional activities and understand the impact of project decisions on the overall clinical trial. Look for opportunities to expand and deepen clinical trial process expertise across functional teams, regions, and external partners and make decisions on process and issues affecting study implementation and execution.
  • Be knowledgeable on the global and regional operating model; coordinate and facilitate obtaining regional input to provide to the study teams.
  • Project Management, and Regional Operational Knowledge

DUTIES:

  • Broader responsibilities at Therapeutic Area/ Molecule/Indication level (e.g. attending relative critical chain network builds, providing input on strategy).
  • Use project management skills, processes, and tools to develop and execute local, regional, and/or global clinical trials (CT) as described:
  • Scope - Understand the scope of work required to complete the clinical trial successfully. Monitor the status and make adjustments and changes (per change control process) as needed to meet the deliverables of the trial.
  • Timeline – Develop and track global trial enrollment plan by gaining alignment and integrating inputs across functions and geographies.