ZipRecruiter

Log In

1

Clinical Research Associate Neuroscience Jobs (NOW HIRING)

Ohio State University

Research Associate- Neuroscience Department:Medicine | School Biomedical Sciences Neuroscience Research Associate participates in planning, design, execution, and management of research projects in a ...

Alto Neuroscience, Inc.

Clinical Research Associate

$80/hr

About Alto Neuroscience, Inc. At Alto Neuroscience, you will play a pivotal role in advancing ... Primary Role The Clinical Research Associate (CRA) is responsible for the oversight of assigned ...

CTTX Health

Clinical Research Associate

Cambridge, MA · On-site

... looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company ... in neuroscience. What You'll Do: * Conduct site initiation, monitoring, and close-out visits to ...

CTTX Health

Clinical Research Associate

Cambridge, MA · On-site

... looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company ... in neuroscience. What You'll Do: * Conduct site initiation, monitoring, and close-out visits to ...

CTTX Health

Clinical Research Associate

Cambridge, MA · On-site

... looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company ... in neuroscience. What You'll Do: * Conduct site initiation, monitoring, and close-out visits to ...

ScholarshipsAds Inc.

$100 - $125/hr

Clinical Research Associate (CRA) Location: Redwood City, CA Length: 6 Month Contract Were seeking a Clinical Research Associate (CRA) with strong clinical monitoring experience to support a growing ...

Emmes

Sr. Clinical Research Associate

Rockville, MD · On-site +1

... neuroscience. Through our two business units- Emmes, a full-service CRO , and Veridix AI, our ... The Senior Clinical Research Associate (CRA) is responsible for monitoring clinical study sites ...

Emmes

Sr. Clinical Research Associate

Rockville, MD · On-site

$80 - $100/hr

... neuroscience. Through our two business units-- Emmes, a full-service CRO , and Veridix AI, our ... The Senior Clinical Research Associate (CRA) is responsible for monitoring clinical study sites ...

next page

Showing results 1-20

All JobsClinical Research Associate Neuroscience Jobs

Clinical Research Associate Neuroscience information

See salary details

$36K

$94.3K

$143.5K

How much do clinical research associate neuroscience jobs pay per year?

As of Sep 9, 2026, the average yearly pay for clinical research associate neuroscience in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

What cities are hiring for Clinical Research Associate Neuroscience jobs?

Cities with the most Clinical Research Associate Neuroscience job openings:

What states have the most Clinical Research Associate Neuroscience jobs?

States with the most job openings for Clinical Research Associate Neuroscience jobs include:

What are popular job titles related to Clinical Research Associate Neuroscience jobs?

For Clinical Research Associate Neuroscience jobs, the most frequently searched job titles are:

Infographic showing various Clinical Research Associate Neuroscience job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Senior Clinical Research Associate, Neuroscience (Contract)

Remote

Premier Research
Biotechnology Research and Development • 1 - 5K employees
Learn more about Premier Researchexternal

Full-time

Posted 14 days ago

Job description

Premier Research is looking for a Senior Clinical Research Associate, Neuroscience (Contract) to join our Clinical Monitoring, Site Management and SSU team.
You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
  • We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
  • Your ideas influence the way we work, and your voice matters here.
  • As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.
This is a full-time contract position for 6 months.
What You'll Be Doing:
  • Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan (CMP) timelines
  • Responsible for the validity, correctness, and completeness of the clinical data reviewed and collected at assigned sites as dictated by ICH GCP/ISO14155, protocol and client requirements
  • Monitors (remote, on site or other approved mode of monitoring) with a focus on data integrity and subject safety in accordance with local/regional laws and country specific regulations
  • Plans day-to-day activities for monitoring of a clinical study and sets priorities per site
  • Prepares for and conducts on site and/or remote qualification, study initiation, interim monitoring, dosing observation, and close out monitoring visits as directed per CMP
  • Works with the Clinical Lead or equivalent to enhance and proactively manage site visits and trial issues during the monitoring phase

What We Are Searching For:
  • Must be located in CA, NV, GA, or FL
  • Neuroscience monitoring experience highly prioritized
  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required
  • Patient facing, study coordinating experience preferred
  • Knowledge of ICH-GCP/ISO14155, FDA Guidance Documents, EU Directives, local/regional regulations, and drug/device development and clinical monitoring procedures
  • Knowledge of clinical/health systems as well as knowledge of cultural/professional practices appropriate to the country/region where site monitoring activities will be conducted
  • Ability to multitask and work effectively with technology and people in a fast-paced environment with changing priorities, self-starter
  • Travel up to 70-85%

Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status

Apply