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Cns Clinical Research Associate Jobs (NOW HIRING)

Alto Neuroscience, Inc.

Clinical Research Associate

$80/hr

Experience monitoring clinical trials with rater-administered measures Must have experience with CNS Certified Clinical Research Associate (CCRA) credentialing is preferred Proactive in identifying ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. In this role, you will be a key ...

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Cns Clinical Research Associate information

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$12

$31

$55

How much do cns clinical research associate jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for cns clinical research associate in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

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.

More about Cns Clinical Research Associate jobs
What cities are hiring for Cns Clinical Research Associate jobs? Cities with the most Cns Clinical Research Associate job openings:
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What job categories do people searching Cns Clinical Research Associate jobs look for? The top searched job categories for Cns Clinical Research Associate jobs are:
Cns Clinical Research Associate jobs near you
Infographic showing various Cns Clinical Research Associate job openings in the United States 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, with an average salary of $65,604 per year, or $31.5 per hour.

Clinical Research Associate

Alto Neuroscience, Inc.

Remote

$80/hr

Full-time

Re-posted 11 days ago

Job description

About Alto Neuroscience, Inc.
At Alto Neuroscience, you will play a pivotal role in advancing precision psychiatry and improving how mental health disorders are treated. Join us in building the next generation of personalized neuroscience-based therapeutics.
Primary Role
The Clinical Research Associate (CRA) is responsible for the oversight of assigned investigative sites in accordance with all applicable protocols, project plans, Sponsor SOPs, GCP guidelines, and regulatory requirements from site initiation through site close out. The CRA assists the Clinical Trial Manager and/or Clinical Project Manager by managing their assigned clinical sites to ensure enrollment, timely review of data, identification of site issues, and prompt resolution of issues. The CRA is the primary liaison between the clinical investigator and the Sponsor to ensure the recruitment, enrollment, and site activities are executed on time, within budget, and with the highest quality data standards.
What you'll do
  • Perform site management and act as the primary liaison to the investigator and site staff ensuring consistent and effective communication related to enrollment status, issues and other relevant study information
  • Conduct Site Evaluation, Site Initiation, Interim Monitoring, Close-out, and other study-specific visits including the completion of visit reports and follow-up letters after each visit
  • Assist with the preparation of appropriate training materials and provide protocol and study related training including GCP and regulatory requirements to assigned sites
  • Evaluate the quality and integrity of site practices to ensure GCP compliance and escalate any quality issues as appropriate
  • Manage site and study progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • Ensure the collection and maintenance of required essential documents and ensure these documents are filed in the Investigator Site File and Trial Master File
  • Train site staff on proper preparation, handling, storage, and return/destruction of investigational product(s) and verify compliance during monitoring visits
  • Develop a patient recruitment plan in conjunction with the site, address challenges and barriers to enrollment, and report the subject recruitment rate to the Clinical Project Manager
  • Verify that written informed consent is obtained before each subject's participation in the trial
  • Verify that source documents, other trial records, and CRFs are accurate, complete, and legible and that CRF entries reflect the source
  • Determine whether all adverse events (AEs) are appropriately reported within the time periods required by GCP, the protocol, the Ethic Committees (IRB/IEC), Sponsor and the applicable regulatory requirement(s) Ensure deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements are documented and communicated appropriately and take appropriate action to prevent recurrence of the detected deviations
  • Assist with the coordination and conduct of investigator and study meetings, including preparation and presentation of information
  • Collaborate with team members in a mutually supportive and cooperative manner, as required to achieve study and project goals

Location
Remote
Salary Range
$80-125K Base Salary
*depending on qualifications and experience level
Travel Required
60% travel required
(1-2 days per week)
Qualifications
Required Skills:
Experience monitoring clinical trials with rater-administered measures
Must have experience with CNS
Certified Clinical Research Associate (CCRA) credentialing is preferred
Proactive in identifying areas of improvement to drive efficiency within Clinical Operations
Knowledge of the clinical research discipline, GCP, and ICH-E6 is essential
Excellent interpersonal skills required
Proficiency with systems (CTMS, EDC, eTMF) and MS Office (Word, Excel, Outlook)
The CRA must possess the ability to work closely with cross-functional colleagues within a small company, displaying innovative thinking, analytical thinking, a strong sense of responsibility, accountability, and integrity
Education and Experience:
BS in scientific discipline or pharmacy, RN, or BSN degree, or equivalent combination of education and experience
Minimum 2 years of experience, relevant CRO/biotech/pharmaceutical industry, including on-site or remote monitoring experience
Alto Neuroscience is an equal-opportunity employer that does not discriminate on the basis of sex, age, race, color, religion, marital status, sexual orientation, gender identity, pregnancy, disability, or any other characteristic protected by law. We offer a welcoming and inclusive environment in service to one another, our products, the diverse consumers we represent, and the communities we call home. We do all of this with kindness, empathy and respect for each other. The above is intended to describe the general content of and requirements for the performance of this job. It should not be construed as an exhaustive statement of duties, responsibilities or physical requirements.

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