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Cns Trials Jobs (NOW HIRING)

IQVIA

Senior Clinical Project Manager, CNS

Durham, NC

$93K - $232K/yr

We are seeking a US-based Senior Project Manager with proven experience in Central Nervous System (CNS) clinical trials to join IQVIA Biotech. This role is ideal for a seasoned project management ...

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$53.5K

$127.5K

$206.5K

How much do cns trials jobs pay per year?

As of Jun 8, 2026, the average yearly pay for cns trials in the United States is $127,453.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $202,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced by professionals working in CNS clinical trials, and how can they be addressed?

Professionals involved in CNS (central nervous system) clinical trials often face unique challenges such as patient recruitment and retention, as neurological disorders can affect participants' ability to consent and adhere to protocols. Additionally, measuring outcomes objectively is complex due to the variability of CNS disorders. These challenges can be addressed by designing patient-centric studies, using clear communication strategies, and leveraging technologies like electronic patient-reported outcomes and wearable devices to gather more reliable data. Collaborating closely with multidisciplinary teams, including neurologists, psychologists, and data managers, is also key to successful trial execution.

What is the difference between Cns Trials vs Clinical Research Coordinator?

AspectCns TrialsClinical Research Coordinator
Required CredentialsTypically requires clinical trial experience, healthcare background, and sometimes certifications like CCRPUsually requires a bachelor's degree in health or related field; certifications like CCRP are common but not mandatory
Work EnvironmentConducts or oversees clinical trials, often in hospitals, research centers, or pharmaceutical companiesManages daily activities of clinical studies at research sites, hospitals, or clinics
Employer & Industry UsageUsed mainly in pharmaceutical, biotech, and clinical research organizationsCommonly employed in hospitals, research institutions, and clinical trial sites

While both roles are involved in clinical research, Cns Trials typically focus on overseeing or conducting clinical trials, requiring specialized experience and certifications. Clinical Research Coordinators handle the day-to-day management of studies, often with less specialized credentials. Understanding these differences helps in choosing the right career path or job search focus.

What are CNS Trials?

CNS Trials refer to clinical studies that investigate treatments, drugs, or interventions targeting the central nervous system (CNS), which includes the brain and spinal cord. These trials are essential for developing therapies for neurological and psychiatric conditions such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, depression, and schizophrenia. CNS trials typically involve multiple phases to ensure the safety and efficacy of new treatments before they become widely available. The complexity of the CNS and the conditions it affects means these trials often require rigorous protocols and specialized expertise.

What are the key skills and qualifications needed to thrive in CNS Clinical Trials, and why are they important?

To thrive in CNS Clinical Trials, you need a solid background in neuroscience, clinical research methodologies, and a relevant science degree, often supplemented by certifications such as GCP (Good Clinical Practice). Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation is typical. Strong attention to detail, effective communication, and problem-solving abilities help professionals navigate complex studies and work with interdisciplinary teams. These skills and qualifications are crucial for ensuring the integrity, compliance, and successful execution of CNS clinical research.
Infographic showing various Cns Trials job openings in the United States as of May 2026, with employment types broken down into 91% Full Time, 8% Part Time, and 1% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $127,453 per year, or $61.3 per hour.

Clinical Research Assistant (CRA)

Lighthouse Psychiatry Brain Health Center

Gilbert, AZ

$18 - $23/hr

Full-time

Medical

Posted 17 days ago

Job description

Clinical Research Assistant (CRA) (Psychiatry)
Lighthouse Psychiatry
Location: Arizona (On-Site – Outpatient Psychiatry Clinic)
Employment Type: Full-Time
Pay Range: $38,000 – $48,000 annually, based on experience, certifications, and scope of responsibility
Department: Clinical Research & Interventional Psychiatry

About Lighthouse Psychiatry:
Lighthouse Psychiatry is a modern outpatient mental health practice delivering evidence-based and interventional psychiatric care, including medication management, TMS, ketamine/esketamine therapy, psychotherapy, and emerging treatment modalities. Our clinical research program supports sponsor-funded and investigator-initiated trials focused on advancing psychiatric care while maintaining the highest standards of ethics, safety, and regulatory compliance. Our sponsor-funded research efforts focus on phase 2 and 3 clinical trials.
Position Summary:
Lighthouse Psychiatry is seeking a Clinical Research Assistant (CRA) (Psychiatry) to manage and support psychiatric and CNS clinical trials in an outpatient setting. This role oversees day-to-day trial operations, including participant recruitment, informed consent, regulatory documentation, data management, clinical rating (if applicable), and compliance with GCP, IRB, FDA, and HIPAA standards.
Key Responsibilities:
Clinical Trial Coordination:
  • Coordinate psychiatry and mental health clinical trials from study start-up through close-out.
  • Execute study protocols in compliance with ICH-GCP, FDA regulations, IRB approvals, and sponsor requirements.
  • Serve as the primary liaison between investigators, sponsors, CROs, monitors, and IRBs.
  • Prepare for and participate in monitoring visits, audits, and inspections.
Participant Recruitment & Management:
  • Screen, recruit, consent, and enroll participants for psychiatric research studies.
  • Conduct research visits, assessments, and protocol-required procedures under investigator delegation.
  • Phlebotomy, IV access.
  • Collect body fluid samples (blood, urine, etc).
  • Monitor participant safety, report adverse events, and document protocol deviations.
  • Maintain strong participant retention through ongoing communication and follow-up.
Regulatory & Compliance:
  • Prepare and maintain regulatory binders and essential study documentation.
  • Submit IRB applications, amendments, and continuing reviews.
  • Track investigator credentials, training logs, and delegation of authority.
  • Ensure compliance with HIPAA and human-subject protection requirements.
Data Management:
  • Collect and document accurate source data and enter data into EDC systems.
  • Resolve data queries and discrepancies in collaboration with sponsors and monitors.
  • Maintain audit-ready documentation and data integrity.
Collaboration & Research Support:
  • Collaborate with psychiatrists, psychologists, nurses, medical assistants, and administrative staff to integrate research into clinical workflows.
  • Support feasibility assessments, study start-up activities, and investigator-initiated research efforts.

Required Qualifications:
  • Bachelor’s degree in Clinical Research, Psychology, Neuroscience, Public Health, Nursing, or related field.
  • 1–3+ years of clinical research experience, preferably in psychiatry, behavioral health, or CNS trials.
  • Knowledge of GCP, IRB processes, informed consent, and FDA-regulated clinical trials.
  • Phlebotomy certified.
  • Strong organizational and documentation skills.
  • Excellent written and verbal communication abilities.

Preferred Qualifications:
  • Experience in psychiatry, interventional psychiatry, or mental health clinical trials.
  • Familiarity with psychiatric rating scales (MADRS, HAM-D, HAM-A, MINI, PHQ-9, GAD-7, CGI, C-SSRS, PCL-5, ATRQ, etc).
  • Experience with EDC, CTMS, CRIO, EMA Wellness, and electronic source systems.
  • CCRC, CCRP, or equivalent clinical research certification.
  • Outpatient or private-practice research experience.

Key Skills & Competencies (Keywords):
  • Clinical Research Coordinator.
  • CRC.
  • Clinical Research Assistant.
  • CRA.
  • Psychiatry Research.
  • Behavioral Health.
  • CNS Trials.
  • GCP.
  • IRB.
  • FDA Compliance.
  • Informed Consent.
  • Patient Recruitment.
  • EDC.
  • CTMS.
  • Data Entry.
  • Regulatory Binder.
  • Mental Health Research.
  • Outpatient Psychiatry.
  • CRIO.
  • Psychedelics.
  • Clinical Trials.
  • Nurses (RN).
  • Medical Assistant (MA).
  • Post-graduate International Medical Graduate (IMG).

Why Join Lighthouse Psychiatry:
  • Competitive pay aligned with experience and certification.
  • Exposure to cutting-edge psychiatric and interventional research.
  • Collaborative outpatient clinical environment.
  • Career growth opportunities in clinical research and mental health innovation.

Equal Opportunity Employer:
Lighthouse Psychiatry is an equal opportunity employer committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Join Lighthouse Psychiatry clinical research team today!
Competitive pay aligned with experience and certification.

About Lighthouse Psychiatry Brain Health Center:

Lighthouse Psychiatry is dedicated to providing a patient-centric and quality-focused experience that is grounded in safety, personalization, innovation, and clinical research. No two individuals are alike. Thus, our approach to care delivery incorporates customized treatment solutions tailored to the clinical and mental needs and challenges of the individual. Our integrative services including psychiatric medication management, counseling, TMS, qEEG, Spravato, ketamine, ADHD testing and treatment, and clinical research of novel treatments. We treat our patients as people.