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Ptsd Research Assistant Jobs (NOW HIRING)

Grant Writer

Gainesville, GA · On-site

$55K - $65K/yr

... PTSD Foundation of America through the research, preparation, writing, and submission of grant ... applications. * Assist with the preparation of grant reports, stewardship materials ...

Research Support Under close supervision of the PI and senior staff, the SRA I will: * Assist with augmented psychotherapy trials that combine evidence-based PTSD treatments (e.g., exposure-based ...

Research Support Under close supervision of the PI and senior staff, the SRA I will: * Assist with augmented psychotherapy trials that combine evidence-based PTSD treatments (e.g., exposure-based ...

Coordinate and support augmented psychotherapy trials that combine evidence-based PTSD treatments ... Track enrollment, timelines, and milestones ; assist with and help prepare progress reports, RPPRs ...

Coordinate and support augmented psychotherapy trials that combine evidence-based PTSD treatments ... Track enrollment, timelines, and milestones ; assist with and help prepare progress reports, RPPRs ...

Coordinate and support augmented psychotherapy trials that combine evidence-based PTSD treatments ... Track enrollment, timelines, and milestones ; assist with and help prepare progress reports, RPPRs ...

Coordinate and support augmented psychotherapy trials that combine evidence-based PTSD treatments ... Track enrollment, timelines, and milestones ; assist with and help prepare progress reports, RPPRs ...

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Ptsd Research Assistant information

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How much do ptsd research assistant jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for ptsd research assistant in the United States is $21.91, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $25.48 per hour, depending on experience, location, and employer.

What is the difference between Ptsd Research Assistant vs Clinical Research Coordinator?

AspectPtsd Research AssistantClinical Research Coordinator
Required CredentialsTypically a bachelor's degree in psychology, neuroscience, or related field; research experience preferredUsually a bachelor's degree; certification in clinical research is a plus
Work EnvironmentResearch labs, universities, mental health research centersHospitals, clinics, research sites
Employer & Industry UsageAcademic institutions, mental health research organizationsHealthcare facilities, clinical trial sites
Common Search & ComparisonOften compared for research roles in mental health and PTSD studiesCompared for overseeing clinical trials and patient coordination

The main difference is that a Ptsd Research Assistant primarily supports PTSD research projects, focusing on data collection and analysis, while a Clinical Research Coordinator manages the overall clinical trial process, including patient recruitment and compliance. Both roles require research experience, but the coordinator role often involves more administrative responsibilities and direct patient interaction.

What are the key skills and qualifications needed to thrive as a PTSD Research Assistant, and why are they important?

To thrive as a PTSD Research Assistant, you need a background in psychology or related fields, experience with research methodologies, and attention to ethical standards, often supported by a bachelor’s or master’s degree. Familiarity with data analysis software (such as SPSS or R), survey tools, and Institutional Review Board (IRB) protocols is typically required. Strong organizational skills, empathy, and effective communication are vital soft skills for interacting with study participants and collaborating with research teams. These capabilities ensure accurate data collection, ethical treatment of participants, and meaningful contributions to PTSD research.

What does a PTSD Research Assistant do?

A PTSD Research Assistant supports research projects focused on post-traumatic stress disorder (PTSD). Their responsibilities typically include recruiting and interviewing study participants, administering assessments and surveys, collecting and managing data, and assisting with literature reviews. They may also help with data analysis and preparing research findings for publication or presentation. The role is essential for advancing our understanding of PTSD and developing effective treatments.

What are some common challenges faced by a PTSD Research Assistant during data collection and participant interaction?

PTSD Research Assistants often encounter unique challenges during data collection, such as ensuring participant comfort and confidentiality when discussing sensitive trauma-related topics. Building rapport and maintaining ethical boundaries are essential, as participants may experience emotional distress. It is important to be well-versed in trauma-informed care and to follow strict research protocols. Team collaboration with clinicians and principal investigators is common, and regular debriefings help address any difficulties that arise.
More about Ptsd Research Assistant jobs
What cities are hiring for Ptsd Research Assistant jobs? Cities with the most Ptsd Research Assistant job openings:
What are the most commonly searched types of Ptsd Research jobs? The most popular types of Ptsd Research jobs are:
What states have the most Ptsd Research Assistant jobs? States with the most job openings for Ptsd Research Assistant jobs include:
Infographic showing various Ptsd Research Assistant job openings in the United States as of May 2026, with employment types broken down into 91% Part Time, and 9% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $45,571 per year, or $21.9 per hour.

Part-time

Posted 25 days ago


Job description

Position Definition:
The Stress, Trauma, and Resilience Program (STaR Lab) at the San Francisco VA Health Care System (SFVAHCS), in partnership with Northern California Institute for Research and Education, Inc. (NCIRE) and University of California, San Francisco (UCSF), is seeking an experienced Staff Research Associate II (SRA II) to support and help manage clinical and experimental studies on trauma- and stressor-related disorders in Veterans, with a particular focus on PTSD, sleep disturbance, traumatic brain injury (TBI), and fear learning.
Our overarching goal is to develop mechanism-informed, pharmacologically augmented psychotherapies that directly target the neural systems involved in these conditions, with a focus on enhancing fear extinction and related learning processes. Ultimately, we aim to translate this work into more targeted, effective treatments for Veterans with PTSD, insomnia, TBI, and other trauma-related difficulties.
This role is ideal for someone seeking a 50% research / 50% administrative position who has solid prior research experience and wants to play a central role in clinical trial coordination, psychophysiology data collection, and multi-site study operations. Highly motivated candidates may have opportunities to co-author publications and contribute to presentations.
Essential Functions:
Research (~50%)
  • Coordinate and support augmented psychotherapy trials that combine evidence-based PTSD treatments (e.g., exposure-based therapies) with medications that target mechanisms underlying the disorder, including those that facilitate fear extinction.
  • Administer, pilot, and analyze remote psychophysiological fear-conditioning paradigms, including online and lab-based experimental tasks.
  • Set up, monitor, and troubleshoot psychophysiological recording sessions using systems such as Biopac and Lab Streaming Layer (LSL)-based data pipelines.
  • Acquire, process, and organize multi-modal psychophysiological signals, including electrodermal activity (EDA), electromyography (EMG), heart rate (HR), heart rate variability (HRV), facial coding outputs, and remote photoplethysmography (PPG) signals derived from video.
  • Conduct and score clinical interviews and self-report measures assessing PTSD symptoms, trauma exposure, mood, and sleep-related functioning (training provided as needed).
  • Collect, process, and analyze sleep-related data, including actigraphy and EEG-based measures.
  • Assist with and increasingly take ownership of data management and analysis (e.g., REDCap, spreadsheets, data quality checks, and basic statistical software).
  • For candidates with appropriate clinical training, there may be opportunities to be involved in structured clinical assessment and to receive training in manualized, exposure-based psychotherapy protocols, delivering supervised, protocol-guided treatment components as part of the trial.

Administrative (~50%)
  • Coordinate day-to-day study operations, including participant recruitment, screening, scheduling, and follow-up, ensuring that visit windows and protocol requirements are met.
  • Maintain and organize regulatory documents (IRB submissions, amendments, renewals, consent forms) in collaboration with the PI and regulatory staff.
  • Serve as a key liaison with a multidisciplinary team of investigators, clinicians, coordinators, and collaborators across sites.
  • Track enrollment, timelines, and milestones; assist with and help prepare progress reports, RPPRs, and other grant-related documentation.
  • Support NCIRE and VA administrative processes, including onboarding of staff/volunteers, purchasing, and meeting organization (e.g., agendas, notes, action items).

Qualifications:
  • Bachelor's degree in Psychology, Neuroscience, Biology, Public Health, Social Work, or a related field; a Master's degree or PhD is a plus. Individuals with clinical training, particularly in fields such as social work, clinical psychology, or counseling psychology, would also be a good fit, especially if they are interested in integrating clinical assessment and structured psychotherapy into research.
  • At least 2-3 years of experience in research or clinical trial settings, preferably involving mental health, neuroscience, or related clinical populations.
  • Strong organizational skills, attention to detail, and ability to manage multiple tasks and deadlines.
  • Excellent written and verbal communication skills.
  • Demonstrated interest in trauma/PTSD, fear learning, psychophysiology, and/or sleep-related processes.
  • Experience with clinical trial management or coordination (e.g., tracking visit windows, managing protocols, interfacing with sponsors/regulatory teams) is strongly preferred.
  • Experience with psychophysiological data collection or analysis (e.g., Biopac, LSL, EDA, EMG, HR/HRV, facial coding, or remote PPG from video) is strongly preferred; enthusiasm for further developing these skills is essential.
  • Experience with data analysis or programming tools (e.g., MATLAB, Python, R) is highly desirable.
  • Clinical experience with trauma-exposed populations (e.g., Veterans, survivors of interpersonal violence, first responders) is highly beneficial for this role.
  • Comfort working with Veterans and individuals with trauma histories, with professionalism, empathy, and strong interpersonal skills.

VA Onboarding Requirements:
NCIRE is an affiliate organization of the San Francisco VA Health Care System (SFVAHCS), which requires all candidates to complete SFVA onboarding in addition to NCIRE's onboarding process. The SFVA is a federal agency that requires a federal background check, occupational health clearance, vaccines and immunizations, and drug testing for certain positions. Drug testing may include screening for marijuana which remains an illegal substance according to federal law. The failure to pass required drug testing will disqualify candidates from employment.
The base wage range for this position is $25.24 - $40.60 per hour. The wage actually offered to a successful candidate will take into account various relevant and non-discriminatory business factors including, without limitation, the candidate's geographic location, job-related experience, knowledge, and skills, and education, as well as internal equity considerations. A successful candidate may also be eligible to earn additional compensation including bonuses.
NCIRE is an Equal Opportunity Employer. This position requires access to United States Government research under the Veterans Administration. Per Veterans Administration regulations surrounding access to US research, qualified US Citizens will be selected over other individuals eligible to work in the United States. If you are eligible to work in the United States, you may still be considered for this position but only if no qualified US citizens apply.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.