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Cns Clinical Research Associate Jobs in Indiana (NOW HIRING)

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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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Cns Clinical Research Associate information

What is a CNS Clinical Research Associate?

CNS Clinical Research Associates (CRAs) are professionals who oversee and manage clinical trials focused on Central Nervous System (CNS) disorders, such as Alzheimer's, Parkinson's, and multiple sclerosis. They are responsible for monitoring study sites, ensuring compliance with protocols, collecting and verifying data, and maintaining participant safety. CNS CRAs play a crucial role in advancing treatments by facilitating the research process from trial initiation to closeout. They often collaborate with investigators, sponsors, and regulatory bodies to ensure the integrity and quality of clinical research.

What are some common challenges faced by a CNS Clinical Research Associate during multi-site clinical trials?

CNS Clinical Research Associates often encounter challenges such as coordinating communications between multiple study sites, ensuring consistent protocol adherence, and managing complex documentation requirements. Additionally, overseeing trials involving central nervous system disorders can be demanding due to variability in patient populations and strict regulatory standards. Staying organized, proactive in problem-solving, and maintaining close collaboration with site staff and sponsors are key to overcoming these hurdles and ensuring trial success.

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

To thrive as a CNS Clinical Research Associate, you need a strong background in life sciences, clinical research methodology, and understanding of central nervous system (CNS) disorders, typically supported by a relevant degree and experience in clinical trials. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and regulatory compliance certifications are commonly required. Strong organizational skills, attention to detail, and the ability to communicate effectively with multidisciplinary teams set top performers apart. These skills are crucial to ensure accurate data collection, regulatory adherence, and successful coordination of complex CNS clinical studies.

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

AspectCns Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often with certifications like CCRP or RACBachelor's degree, often in health or science fields
Work EnvironmentMonitors clinical trials at multiple sites, often remotely or on-siteManages daily trial activities at a specific site
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites

The Cns Clinical Research Associate primarily oversees multiple trial sites, ensuring protocol compliance and data integrity, often working remotely. In contrast, the Clinical Research Coordinator manages day-to-day trial activities at a single site, including patient recruitment and data collection. Both roles require similar educational backgrounds but differ in scope and responsibilities.

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

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

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

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

Cns Clinical Research Associate jobs near you
Infographic showing various Cns Clinical Research Associate job openings in Indiana as of August 2026, with employment types broken down into 88% Full Time, 4% Part Time, and 8% Contract. Highlights an 71% In-person, and 29% Remote job distribution.

Clinical Research Associate

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Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 14 days ago

Job description

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-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Willingness to travel as required (approximately 60%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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