Clinical Trial Psych Rater
Colton, CA · Remote
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Colton, CA · Remote
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Colton, CA · Remote
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...
Irvine, CA · On-site +1
Coordinates and oversees all clinical trial startup and site closure activities, ensuring that ... Provide strategic direction on field and remote monitoring as required and data collection for all ...
Irvine, CA · On-site +1
Coordinates and oversees all clinical trial startup and site closure activities, ensuring that ... Provide strategic direction on field and remote monitoring as required and data collection for all ...
Irvine, CA · Remote
$120K - $135K/yr
Clinical Trial Administration * Assist with trial start-up, including preparing and submitting ... Perform remote monitoring activities such as source data verification (SDV) and data entry checks ...
Irvine, CA · Remote
$120K - $135K/yr
Clinical Trial Administration * Assist with trial start-up, including preparing and submitting ... Perform remote monitoring activities such as source data verification (SDV) and data entry checks ...
Irvine, CA · On-site +1
Irvine, California, United States of America, Remote (US) Johnson & Johnson MedTech, Neurovascular ... Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan ...
Irvine, CA · On-site +1
Irvine, California, United States of America, Remote (US) Johnson & Johnson MedTech, Neurovascular ... Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan ...
Irvine, CA · On-site +1
Irvine, California, United States of America, Remote (US) Johnson & Johnson MedTech, Neurovascular ... Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan ...
Irvine, CA · On-site +1
Irvine, California, United States of America, Remote (US) Johnson & Johnson MedTech, Neurovascular ... Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan ...
Irvine, CA · On-site +1
S. based, remote position that requires regular travel to clinical trial sites across the country (up to 70%). Applicants must be currently authorized to work in the United States and comfortable ...
Irvine, CA · On-site +1
S. based, remote position that requires regular travel to clinical trial sites across the country (up to 70%). Applicants must be currently authorized to work in the United States and comfortable ...
Irvine, CA · On-site +1
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Irvine, CA · On-site +1
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Irvine, CA · On-site +1
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Irvine, CA · On-site +1
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Remote Summary: Reporting to the Senior Director of Clinical Affairs, the Manager, Clinical Affairs ... trial sites. * Collaborate with cross functional team leaders to ensure harmonization of processes ...
Remote Summary: Reporting to the Senior Director of Clinical Affairs, the Manager, Clinical Affairs ... trial sites. * Collaborate with cross functional team leaders to ensure harmonization of processes ...
Irvine, CA · On-site +1
$145K/yr
Remote Summary: Reporting to the Senior Director of Clinical Affairs, the Manager, Clinical Affairs ... trial sites. * Collaborate with cross functional team leaders to ensure harmonization of processes ...
Irvine, CA · On-site +1
$145K/yr
Remote Summary: Reporting to the Senior Director of Clinical Affairs, the Manager, Clinical Affairs ... trial sites. * Collaborate with cross functional team leaders to ensure harmonization of processes ...
Irvine, CA · On-site +1
$85K - $117K/yr
... and highquality trial designs. Let's talk about some of the key responsibilities of the role ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Irvine, CA · On-site +1
$85K - $117K/yr
... and highquality trial designs. Let's talk about some of the key responsibilities of the role ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Irvine, CA · On-site +1
$85K - $117K/yr
... and highquality trial designs. Let's talk about some of the key responsibilities of the role ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Irvine, CA · On-site +1
$85K - $117K/yr
... and highquality trial designs. Let's talk about some of the key responsibilities of the role ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Hesperia, CA · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.
Hesperia, CA · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.
San Bernardino, CA · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.
San Bernardino, CA · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.
Ontario, CA · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.
Ontario, CA · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... clinical trial analysis, regulatory submission reviews, and observational study assessments.
$30.09 - $36.48
4% of jobs
$36.48 - $42.86
6% of jobs
$42.86 - $49.25
7% of jobs
$54.03 is the 25th percentile. Wages below this are outliers.
$49.25 - $55.63
9% of jobs
$55.63 - $62.01
15% of jobs
The median wage is $64.83 / hr.
$62.01 - $68.40
18% of jobs
$72.94 is the 75th percentile. Wages above this are outliers.
$68.40 - $74.78
21% of jobs
$74.78 - $81.16
7% of jobs
$81.16 - $87.55
6% of jobs
$87.55 - $93.93
3% of jobs
$93.93 - $100.31
2% of jobs
$30
$65
$100
The top searched job categories for Remote Clinical Trial Navigator jobs in Riverside, CA are:
Cities near Riverside, CA with the most Remote Clinical Trial Navigator 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