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Neuroscience Clinical Research Jobs (NOW HIRING)

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

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 ...

Research Assistant

Miami, FL · On-site

$18.50 - $25.25/hr

Research Assistant Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I ... Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with ...

Research Assistant

Miami, FL

$18.50 - $25.25/hr

Research Assistant Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I ... Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with ...

Laboratory Technician

Miami, FL

$18.25 - $24.25/hr

Laboratory Technician Evolution Research Group (ERG) is dedicated to delivering high-quality Phase ... Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with ...

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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 Sep 2, 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.

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.

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:

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, 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 $107,336 per year, or $51.6 per hour.

Clinical Research Nurse

Evolution Research Group

Lemon Grove, CA • On-site

$37 - $42/hr

Full-time

Medical, Dental, Retirement, PTO

Posted 10 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:

The Registered Nurse will perform a variety of activities related to the clinical area, including medical support systems and assisting medical personnel with study participants care duties as assigned. Incumbents work under supervision of clinical staff, performing routine duties and primarily, referring questions and problems to the Clinical Research Coordinator assigned to study or the PI. 

Responsibilities:

Clinical: 

  • Perform study events and collects clinical data as per protocol requirements.
  • Administer study drug as assigned.
  • When assigned, serve as Pharmacy Staff.
  • Discuss and administer Informed Consent Form, as assigned (dependent on site) 
  • Notify appropriate staff of abnormal results while collecting data, adverse events, or unusual incidents.
  • Assure minimal discomfort for study participants while performing all duties.
  • Working knowledge of telemetry monitoring and interpretation of tracings
  • Maintain safety and well-being of study participants during assigned shift.
  • Knowledge of Holter monitor skills.
  • Prepare participants for events.
  • Understand all functions of telemetry monitoring machine.
  • Collect all telemetry tracings for licensed personnel to review.
  • Ability to use proper advanced life support equipment and supplies.
  • Maintain skills in the use of ECG machine, taking accurate vital signs and IV insertion.
  • Keep apprised of all new OSHA, BLS, ACLS and GCP/ICH rules, regulations, and procedures.
  • Perform initial evaluation of adverse event.
  • Knowledge of drug reactions and the synergistic effects of drugs combined with other medicines.
  • Ability to apply basic principles of mathematics to the calculation of problems associated with medication dosages.
  • Must be capable of providing advanced life support emergency medical services, including conducting of and interpreting ECGs, electrical interventions to support cardiac functions, performing advanced endotracheal intubations in airway management and relief of pneumothorax and administering of appropriate intravenous fluids and drugs under direction of a designated physician.
  • Stay focused while assuming the leadership role inherent in carrying out the functions of the position.
  • Provide top quality care and concurrently handle high levels of stress.

Administrative: 

  • Read and understand each protocol in which he/she is involved.
  • Maintain knowledge and understanding of SOP for data collection.
  • Maintain accurate and neat documentation records as required by the protocol.
  • Follow proper safety procedures and report to supervisor immediately all injuries, unsafe practices, and unusual incidents.
  • Know OSHA and GCP/ICH rules and regulations and comply with all requirements.
  • Perform inventory of supplies needed and report deficiencies to clinical staff supervisor.
  • Stay on duty/assigned shift until relieved by oncoming staff.

Educational: 

  • Maintain current licensure, registration and/or certification within educational background.
  • Maintain current BLS and/or ACLS certification
  • Maintain necessary CEU’s for licensure, registration and/or certification.
  • Assist in training new Paramedics, Emergency Medical Technicians (EMT), Medical/ Nursing Assistants (MA, NA) and Phlebotomy Technician
  • Actively participate in ongoing Quality Assurance Program, HIPAA, and Compliance Programs
  • Keep apprised of all new OSHA and GCP/ICH Rules and Regulations
  • Attend all appropriate team meetings regarding study protocols.
  • Learn and maintain skills in use of EKG machines and taking accurate vital signs.
  • Read and understand site policy and procedures manuals, SOP manual, and employee handbook.

Additional Responsibilities:

  • Comply with all site policies and procedures, especially those regarding protocol confidentiality.
  • Demonstrate a caring, professional attitude and behavior toward study participants and staff, actively contributing to the well-being and dignity of the clinic.
  • Maintain an overall good work attitude, promoting cooperation and professionalism and interactions with other staff members.
  • Maintain assigned work areas in a clean, safe condition, and report any potential hazards immediately.
  • Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

Skills and Qualifications:

  • Education and experience
    • Licensure as a Registered Nurse (RN) in the applicable state with ACLS Certification and a minimum of one year experience as an 
    • RN in a medical facility
    • Clinical Research experience preferred but not required.
    • ACLS certification required.
  • Requirements
    • Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines. 
    • Knowledgeable in medical terminology 
    • Good organizational and interpersonal skills 
    • Attention to detail. 
    • Excellent communication skills (interpersonal, written, verbal) 
    • Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as RealTime)