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Neuroscience Clinical Research Jobs (NOW HIRING)

The Mind Research Network

Professor

Albuquerque, NM · On-site

... neuroscience, clinical investigation, and nonclinical model systems. Close collaborations across MRN, Lovelace Biomedical Research Institute, and the University of New Mexico create unique ...

Insight

Clinical Research Assistant

Flint, MI

Insight Institute of Neuroscience amp; Neurosurgery (IINN) aims to advance, challenge, and ... The Clinical Research Assistant will support the clinical research team at our Research Dearborn ...

Insight

Clinical Research Assistant

Flint, MI · On-site

Insight Institute of Neuroscience & Neurosurgery (IINN) aims to advance, challenge, and ... The Clinical Research Assistant will support the clinical research team at our Research Dearborn ...

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 ...

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Neuroscience Clinical Research information

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$49K

$107.3K

$189K

How much do neuroscience clinical research jobs pay per year?

As of Aug 11, 2026, the average yearly pay for neuroscience clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

How do I become a neuroscience clinical researcher?

To become a neuroscience clinical researcher, typically a candidate needs a doctoral degree such as a Ph.D. or M.D. in neuroscience, psychology, or a related field. Relevant experience includes conducting clinical trials, understanding research protocols, and familiarity with regulatory requirements like IRB approval; additional certifications in clinical research can also be beneficial.

Does neuroscience clinical research pay well?

Neuroscience clinical research positions typically offer competitive salaries that vary based on experience, education, and location. Entry-level roles may start lower, but experienced researchers or those with advanced degrees can earn higher wages, especially in specialized or senior positions within research institutions or pharmaceutical companies.

What is a neuroscience clinical research?

A Neuroscience Clinical Research job involves designing, conducting, and analyzing clinical studies focused on neurological disorders and brain function. Professionals in this role work with patients, collect and interpret data, and ensure compliance with regulatory guidelines. They may collaborate with physicians, scientists, and pharmaceutical companies to develop new treatments and interventions. This job requires a strong background in neuroscience, clinical trial methodologies, and ethical research practices.

What does a neuroscience clinical research do?

A Neuroscience Clinical Research professional is typically involved in designing and coordinating clinical trials, recruiting and screening study participants, collecting and managing research data, and ensuring adherence to study protocols and ethical guidelines. You’ll often collaborate closely with clinicians, research coordinators, and data analysts, and may assist in preparing regulatory submissions or scientific publications. Additionally, you may monitor study progress, troubleshoot protocol deviations, and contribute to grant writing or obtaining project funding. This diverse set of responsibilities ensures ongoing learning and engagement within a multidisciplinary team environment.

What are the key skills and qualifications needed for neuroscience clinical research?

To thrive in Neuroscience Clinical Research, you need a solid background in neuroscience or related biomedical sciences, experience with clinical research methods, and often an advanced degree (such as MSc or PhD). Familiarity with data analysis tools (like SPSS or MATLAB), electronic data capture systems, and Good Clinical Practice (GCP) certification is highly valued. Strong organizational skills, attention to detail, effective communication, and the ability to work collaboratively are crucial soft skills. These capabilities ensure accurate data collection, ethical compliance, and successful coordination of clinical trials, which are vital for advancing neurological research and patient care.

More about Neuroscience Clinical Research jobs
What cities are hiring for Neuroscience Clinical Research jobs? Cities with the most Neuroscience Clinical Research job openings:
What are the most commonly searched types of Neuroscience Clinical Research jobs? The most popular types of Neuroscience Clinical Research jobs are:
What states have the most Neuroscience Clinical Research jobs? States with the most job openings for Neuroscience Clinical Research jobs include:
What job categories do people searching Neuroscience Clinical Research jobs look for? The top searched job categories for Neuroscience Clinical Research jobs are:
Neuroscience Clinical Research jobs near you
Infographic showing various Neuroscience Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Assistant Clinical Research Coordinator

Evolution Research Group

Miami, FL • On-site

$22 - $26.50/hr

Full-time

Medical, Dental, Retirement, PTO

Posted 20 days ago

Job description

About Company:

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S.and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.


Job Description:

ERG is the largest independent clinical research site services company focused on special populations and is the market leader in CNS.  With 18 wholly owned clinical sites, we conduct in-patient and out-patient phase I-IV clinical research studies. Our mission is to provide the highest quality execution of clinical trials in all clinical research phases aimed at helping sponsor companies to get their life saving or life enhancing drugs to market as quickly and safely as possible. 

The Assistant Coordinator participates in clinical research studies conducted by the Clinical Research Coordinator. They assist and perform a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data.

Responsibilities:

Administrative:

  • Monitor and ensure study data is collected following plan of care, guidelines and identified group resources
  • Serve in rotation with assistant clinical coordinators and clinical research coordinators
  • Serve as liaison between assigned clinical research coordinator and all clinical departments
  • Participate in collaborative team efforts with other departments
  • Discuss and administer Informed Consent Form
  • Check and ensure that procedure areas are properly stocked with study supplies and equipment (i.e. blood tubes, kits, study flowsheets, ECG machines, BP cuffs, etc.)
  • Assist assigned Clinical Research Coordinator review study schedules to ensure that study procedures are properly staffed
  • Assist assigned Clinical Research Coordinator with the creation and/or review of study flowsheets to ensure study is conducted according to protocol requirements
  • Anticipate, recognize, and resolve issues
  • Reads and understands each protocol in which she/he is involve
  • Follow established guidelines in the collection of clinical data and/or administration of clinical studies
  • Performs all other duties as assigned

Clinical Responsibilities

  • Support adverse event reporting and informed consent administration
  • Notify staff of abnormal results or incidents
  • Ensure participant comfort and readiness for procedures
  • Set up supplies and procedure areas per protocol
  • Perform venipuncture, vital signs, ECG, and other assessments
  • Communicate with participants to explain procedures and gather data
  • Assist with patient care and emergency measures as needed
  • Attend study initiation meetings and perform study-related tasks
  • Provide high-quality care under pressure

Educational:

  • Maintains current licensure, registration and/or certification within educational background
  • Maintains current BLS and/or ACLS certification
  • Maintains necessary CEU’s for licensure, registration and/or certification
  • Actively participates on CPMI’s ongoing Quality Assurance Program, HIPAA and Compliance Programs
  • Keeps apprised of all new OSHA and GCP/ICH rules and regulations
  • Attends all appropriate team meetings regarding study protocols
  • Maintains skills in use of EKG machines, Holter hook-up and monitoring, diabetic monitoring and taking accurate vital signs
  • Reads and understands CPMI policy and procedures manuals, SOP manual and employee handbook