Clinical Trial Psych Rater
Colton, CA · Remote
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Colton, CA · Remote
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Colton, CA · Remote
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
Anaheim, CA · On-site
$90 - $140/hr
Clinical Trial Agreements * Research Finance * Healthcare Administration * Grants Administration Hard Skills * Budget Development * Financial Analysis * Contract Negotiation * Cost Analysis * Trial ...
Anaheim, CA · On-site
$90 - $140/hr
Clinical Trial Agreements * Research Finance * Healthcare Administration * Grants Administration Hard Skills * Budget Development * Financial Analysis * Contract Negotiation * Cost Analysis * Trial ...
Irvine, CA · Remote
$120K - $135K/yr
Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...
Irvine, CA · Remote
$120K - $135K/yr
Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...
Irvine, CA · On-site
$120K - $135K/yr
Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...
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Irvine, CA · On-site
$120K - $135K/yr
Clinical Trial Administration * Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility ...
Irvine, CA · On-site
$35 - $40/hr
Coordinate clinical trial device procurement, shipments, tracking, and returns. * Maintain TMF and clinical study documentation . * Monitor study inventory and assist with forecasting. * Track device ...
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Irvine, CA · On-site
$35 - $40/hr
Coordinate clinical trial device procurement, shipments, tracking, and returns. * Maintain TMF and clinical study documentation . * Monitor study inventory and assist with forecasting. * Track device ...
Irvine, CA · On-site +1
Coordinates and oversees all clinical trial startup and site closure activities, ensuring that ... Oversee the planning of start-up activities (e.g., protocols, informed consents, contracts, scope ...
Irvine, CA · On-site +1
Coordinates and oversees all clinical trial startup and site closure activities, ensuring that ... Oversee the planning of start-up activities (e.g., protocols, informed consents, contracts, scope ...
Irvine, CA · On-site
$35 - $40/hr
... clinical trial workflows and make a direct impact on healthcare innovation. This on-site ... and assist with other clinical study tasks as needed. Required Skills and Experience - At least 2 ...
Irvine, CA · On-site
$35 - $40/hr
... clinical trial workflows and make a direct impact on healthcare innovation. This on-site ... and assist with other clinical study tasks as needed. Required Skills and Experience - At least 2 ...
Irvine, CA · On-site
... ALIGN-AR Pivotal Trial, JENA-VAD Registry, ALIGN-AR EFS Trial, and the ARTIST Trial. Job ... endpoint-related data. * Assist the Clinical Safety team in daily safety reviews, data ...
Irvine, CA · On-site
... ALIGN-AR Pivotal Trial, JENA-VAD Registry, ALIGN-AR EFS Trial, and the ARTIST Trial. Job ... endpoint-related data. * Assist the Clinical Safety team in daily safety reviews, data ...
Riverside, CA · On-site
$20 - $22/hr
Obtains CVs (Curriculum Vitae) of external Investigators and other contract personnel and their ... Works closely with study sponsor/CRO and key clinical trial personnel on relevant regulatory ...
Riverside, CA · On-site
$20 - $22/hr
Obtains CVs (Curriculum Vitae) of external Investigators and other contract personnel and their ... Works closely with study sponsor/CRO and key clinical trial personnel on relevant regulatory ...
Riverside, CA · On-site
$20 - $22/hr
Obtains CVs (Curriculum Vitae) of external Investigators and other contract personnel and their ... Works closely with study sponsor/CRO and key clinical trial personnel on relevant regulatory ...
New
Riverside, CA · On-site
$20 - $22/hr
Obtains CVs (Curriculum Vitae) of external Investigators and other contract personnel and their ... Works closely with study sponsor/CRO and key clinical trial personnel on relevant regulatory ...
New
Riverside, CA · On-site
$20 - $22/hr
Obtains CVs (Curriculum Vitae) of external Investigators and other contract personnel and their ... Works closely with study sponsor/CRO and key clinical trial personnel on relevant regulatory ...
Riverside, CA · On-site
$20 - $22/hr
Obtains CVs (Curriculum Vitae) of external Investigators and other contract personnel and their ... Works closely with study sponsor/CRO and key clinical trial personnel on relevant regulatory ...
... quality trial delivery. Job Requirements * Licensure: Active, unencumbered license to practice as a Nurse Practitioner (NP) or Physician Assistant (PA-C) in California. * Clinical Skills:
... quality trial delivery. Job Requirements * Licensure: Active, unencumbered license to practice as a Nurse Practitioner (NP) or Physician Assistant (PA-C) in California. * Clinical Skills:
Irvine, CA · On-site
$125K - $140K/yr
... quality trial delivery. Job Requirements * Licensure: Active, unencumbered license to practice as a Nurse Practitioner (NP) or Physician Assistant (PA-C) in California. * Clinical Skills:
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Irvine, CA · On-site
$125K - $140K/yr
... quality trial delivery. Job Requirements * Licensure: Active, unencumbered license to practice as a Nurse Practitioner (NP) or Physician Assistant (PA-C) in California. * Clinical Skills:
Maintain Trial Master Files and trackers for clinical trials. * Manage trial-related regulatory ... * Assist field clinical monitors in preparation for site training and monitoring visits * Support ...
Maintain Trial Master Files and trackers for clinical trials. * Manage trial-related regulatory ... * Assist field clinical monitors in preparation for site training and monitoring visits * Support ...
As we expand trial access within Irvine's Chinese-speaking community, we are hiring a Bilingual ... Operational & Enrollment Support: Assist with site enrollment initiatives, community outreach ...
New
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As we expand trial access within Irvine's Chinese-speaking community, we are hiring a Bilingual ... Operational & Enrollment Support: Assist with site enrollment initiatives, community outreach ...
New
$12.04 - $17.46
4% of jobs
$17.46 - $22.89
15% of jobs
$25.60 is the 25th percentile. Wages below this are outliers.
$22.89 - $28.32
13% of jobs
$28.32 - $33.74
8% of jobs
The median wage is $36.76 / hr.
$33.74 - $39.17
19% of jobs
$39.17 - $44.59
13% of jobs
$46.76 is the 75th percentile. Wages above this are outliers.
$44.59 - $50.02
10% of jobs
$50.02 - $55.45
5% of jobs
$55.45 - $60.87
11% of jobs
$60.87 - $66.30
1% of jobs
$66.30 - $71.72
1% of jobs
$12
$39
$71
| Aspect | Contract Clinical Trial Assistant | Clinical Trial Assistant |
|---|---|---|
| Credentials | Typically requires a relevant degree or certification in life sciences or healthcare | Same as Contract CTA, often requiring similar qualifications |
| Work Environment | Contract-based, often temporary assignments at pharmaceutical or biotech companies | Permanent or temporary roles within clinical research organizations or sponsors |
| Employer & Industry Usage | Used by CROs, pharma companies for project-specific needs | Common in clinical research settings, both permanent and contract roles |
| Search & Comparison Intent | Often searched for contract roles, project-based work | Broader search for clinical trial support roles |
The main difference between a Contract Clinical Trial Assistant and a Clinical Trial Assistant lies in employment type and duration. Contract CTAs work on temporary, project-specific assignments, while Clinical Trial Assistants may hold permanent or longer-term positions. Both roles require similar qualifications and are integral to clinical research teams.
For Contract Clinical Trial Assistant jobs in Riverside, CA, the most frequently searched job titles are:
The top searched job categories for Contract Clinical Trial Assistant jobs in Riverside, CA are:
Cities near Riverside, CA with the most Contract Clinical Trial Assistant job openings:
8.1
Based on 53 frontline employees who took The Breakroom Quiz
62nd of 226 rated it services
Location: Remote/Virtual
Hours: Estimated 10-16 hours per month
Role: Clinical Specialist
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
Position Overview
The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation.
Key Responsibilities
Participate in all required orientation, training, and calibration activities.
Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.
Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.
Complete assigned tasks and rater interactions according to schedule.
Submit all required documentation accurately and on time.
Required Qualifications
Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.
Experience:
Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically MINI; MADRS; CAPS; PCL-5; CSSRS; CGI: OR MINI; PANSS; AIMS; BARS; LSAS; PGI-S)
Minimum 3 years of clinical experience with psychiatric populations.
Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).
Experience in CNS trials preferred.
Skills:
Strong interpersonal and communication skills for professional interaction at all levels.
Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Proficiency with Windows and Microsoft Office applications.
Language Requirement
Current openings require fluency in English and native-level proficiency in German.
#LI-DNP #LI-Remote #LI-HCPN
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Health care and social assistance
10,000+ Employees
Durham, NC, US