Neurology Clinical Research Assistant — Part-Time, On-Site

NeuroMind Clinical Trials; Houston (TX); On-site; USD 25,000 - 39,000; Part time

Job summary

NeuroMind Clinical Trials in Houston, TX seeks a part-time Clinical Research Assistant to support daily operations of neurological trials on-site. You will assist with participant scheduling and check-in, prepare examination spaces, and maintain study documentation, data collection, and basic lab tasks under supervision, ensuring protocol adherence and participant safety.

Strong organization, attention to detail, and effective communication with participants and clinical staff are essential in

Qualifications

• Interpersonal and communication skills to interact with participants and clinical teams.
• Knowledge of medical terminology relevant to neurology and healthcare settings.
• Experience in data collection, documentation, and following study protocols.
• Basic laboratory skills such as handling specimens and following safety procedures.
• Reliable, organized, able to use computer applications and follow written/verbal instructions.

Responsibilities

• Assist with participant scheduling and check-in for neurological trials.
• Prepare examination rooms and materials for visits and procedures.
• Maintain accurate study documentation and data collection records.
• Help with basic laboratory procedures under supervision.
• Ensure adherence to study protocols and regulatory guidelines.
• Communicate with participants and clinical staff; manage study files and inventory.

Skills

Interpersonal skills

Communication

Medical terminology

Neurology knowledge

Research skills

Laboratory skills

Reliability

Organization

Computer skills

EHR proficiency

Follow instructions

Education

Health sciences program

Psychology program

Biology program

Related field

Tools

EHR software

Data entry tools

Job description

NeuroMind Clinical Trials in Houston, TX seeks a part-time Clinical Research Assistant to support daily operations of neurological trials on-site. You will assist with participant scheduling and check-in, prepare examination spaces, and maintain study documentation, data collection, and basic lab tasks under supervision, ensuring protocol adherence and participant safety.

Strong organization, attention to detail, and effective communication with participants and clinical staff are essential in