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Cns Clinical Research Associate Jobs in Indiana (NOW HIRING)

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Cns Clinical Research Associate information

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 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 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 Coordinator

Innovative Hematology, Inc.

Indianapolis, IN • On-site

$23.25 - $30.75/hr

Full-time

Re-posted 11 days ago

Job description

About IHI

At Innovative Hematology, Inc. (IHI), we offer a future where people with rare blood disorders flourish. Our experts provide the highest quality comprehensive services and holistic care to patients with bleeding, clotting and other hematologic disorders, and to their families.

What You Will Do

As a Clinical Research Coordinator, you will be responsible for executing research projects under the direction of the primary investigator and for performing in accordance to study regulatory processes, standard operating procedures, and study protocols.

The Opportunity

  • Participate in the planning and execution of research projects under the direction of the Medical Director and the primary investigator.
  • Function as an integral part of the research and comprehensive care teams, working with colleagues to meet deadlines and maintain a flexible schedule based on the needs of patients, the department, and IHI.
  • Create a study budget in InfoED in collaboration with the finance department. Work with the finance department to assist with billing, invoicing, tracking status on payments due or past due, documenting patient stipend requests, and charting completed study visits.
  • Assess patients for inclusion and exclusion criteria to determine study eligibility, and work cooperatively with the comprehensive team to coordinate study-related patient care. Explain informed consent for each study participant; document refusals according to protocol.
  • Ensure accurate and prompt communication with patients, the primary investigator, research manager, external contacts, study sponsors, and monitors.
  • Prepare study-related documentation such as protocol worksheets, procedural manuals, drug dispensation records, regulatory forms, adverse event reports; submit all relevant study documents to the institutional review board.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices. Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
  • Participate in internal quality assurance; review monitor reports for trends across studies.

Requirements

  • Minimum Associate’s degree in related field required.
  • Minimum 1 year of related experience required.
  • Valid Indiana Driver’s license and automobile insurance required.
  • All IHI employees are expected to enable multi-factor authentication via their personal smart phone/smart device in order to access IHI systems as a requirement of the role. 

Benefits

IHI is a not-for-profit program based in Indianapolis and offers a competitive salary and benefit package.

IHI is the only federally designated comprehensive hemophilia program in Indiana and serves the entire state through services available in Indianapolis and at outreach clinics.

IHI is a leader in hemophilia care, education and clinical research and has a dedicated on-site multidisciplinary staff to ensure availability of a wide range of required services.

IHI participates in national and international clinical research, including new infusion products and therapies, investigation of long-term outcomes, and the impact of associated conditions. The IHI research program provides patients access to new therapies, and an opportunity to improve care. Our center has more than 50 clinical research projects involving bleeding disorders, sickle cell disease, thrombosis and more.

Innovative Hematology, Inc. is an Equal Opportunity Employer.