Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Specialist, Clinical Safety
Irvine, CA · On-site
Experience with EDC (Electronic Data Capture) platforms for clinical trial management and safety reporting. * Basic understanding of clinical trial design and statistical concepts as applied to ...
Specialist, Clinical Safety
Irvine, CA · On-site
Experience with EDC (Electronic Data Capture) platforms for clinical trial management and safety reporting. * Basic understanding of clinical trial design and statistical concepts as applied to ...
Specialist, Clinical Safety
Irvine, CA · On-site
$100K/yr
Experience with EDC (Electronic Data Capture) platforms for clinical trial management and safety reporting. * Basic understanding of clinical trial design and statistical concepts as applied to ...
Specialist, Clinical Safety
Irvine, CA · On-site
$100K/yr
Experience with EDC (Electronic Data Capture) platforms for clinical trial management and safety reporting. * Basic understanding of clinical trial design and statistical concepts as applied to ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Associate Clinical Research Specialist
Irvine, CA · On-site
$38 - $43/hr
Medical
Dental
Vision
Life
Retirement
Trial Master File (TMF) management. * Good Documentation Practices. * Clinical Trial Management System (CTMS). * Electronic Data Capture (EDC). * Problem-solving and critical thinking skills.
New
Quick apply
Associate Clinical Research Specialist
Irvine, CA · On-site
$38 - $43/hr
Medical
Dental
Vision
Life
Retirement
Trial Master File (TMF) management. * Good Documentation Practices. * Clinical Trial Management System (CTMS). * Electronic Data Capture (EDC). * Problem-solving and critical thinking skills.
New
Nephrologist(Clinical Trial) - Pomona, CA Compensation: $100-$200/hr or based on market standard rates Commitment: 0-8 hours/weekStart Date: Within 0-6 months Position Summary We are seeking a board ...
Nephrologist(Clinical Trial) - Pomona, CA Compensation: $100-$200/hr or based on market standard rates Commitment: 0-8 hours/weekStart Date: Within 0-6 months Position Summary We are seeking a board ...
Clinical Research Associate
Irvine, CA · Remote
$120K - $135K/yr
The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Track and manage trial documentation, including but not limited to site contracts, investigator ...
Clinical Research Associate
Irvine, CA · Remote
$120K - $135K/yr
The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Track and manage trial documentation, including but not limited to site contracts, investigator ...
Clinical Research Associate
Irvine, CA · On-site
$120K - $135K/yr
The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Track and manage trial documentation, including but not limited to site contracts, investigator ...
Clinical Research Associate
Irvine, CA · On-site
$120K - $135K/yr
The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Track and manage trial documentation, including but not limited to site contracts, investigator ...
Spec 3, Clinical Research
Irvine, CA · On-site
Medical
Life
Retirement
This role is responsible for organizing, reviewing, and maintaining clinical documentation within the Electronic Trial Master File (eTMF) and Clinical Trial Management System (CTMS) to ensure ...
Spec 3, Clinical Research
Irvine, CA · On-site
Medical
Life
Retirement
This role is responsible for organizing, reviewing, and maintaining clinical documentation within the Electronic Trial Master File (eTMF) and Clinical Trial Management System (CTMS) to ensure ...
Senior Associate, Clinical Research
Irvine, CA · On-site
$95K/yr
Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current. * Conduct ...
Senior Associate, Clinical Research
Irvine, CA · On-site
$95K/yr
Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current. * Conduct ...
Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current. * Conduct ...
Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current. * Conduct ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$85K - $90K/yr
At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial ... studies as the primary coordinator required * High school diploma or GED required * Strong ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$85K - $90K/yr
At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial ... studies as the primary coordinator required * High school diploma or GED required * Strong ...
Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...
Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$85K - $90K/yr
At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial ... studies as the primary coordinator required * High school diploma or GED required * Strong ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$85K - $90K/yr
At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial ... studies as the primary coordinator required * High school diploma or GED required * Strong ...
Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...
Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...
Associate, Clinical Research
Irvine, CA · On-site
$75K/yr
Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current. * Conduct ...
Associate, Clinical Research
Irvine, CA · On-site
$75K/yr
Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current. * Conduct ...
Clinical Trial Manager information
See Riverside, CA salary details
$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
How much do clinical trial manager jobs pay per hour?
As of Aug 12, 2026, the average hourly pay for clinical trial manager in Riverside, CA is $65.22, according to ZipRecruiter salary data. Most workers in this role earn between $52.93 and $73.46 per hour, depending on experience, location, and employer.
What does a clinical trial manager do?
A clinical trial manager, or CTM, oversees research and each phase of clinical drug tests at a hospital. They work closely with both the doctors and clinicians who are performing the trial, as well as the sponsor of the study, which is typically a pharmaceutical company or other health care organization. As a CTM, duties and responsibilities include planning and managing the trial, making sure that the test meets all government standards, and determining if it was successful. Clinical trial managers also hire, train, and evaluate the members of the clinical team.
What are the key skills and qualifications needed to thrive as a clinical trial manager, and why are they important?
To thrive as a Clinical Trial Manager, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's or master's degree. Familiarity with clinical trial management systems (CTMS), regulatory requirements like GCP, and certifications such as ACRP or SOCRA are highly beneficial. Strong organizational skills, attention to detail, leadership, and effective communication are critical soft skills for managing teams and stakeholders. These skills ensure trials are conducted ethically, efficiently, and compliantly, leading to successful study outcomes.
What does a clinical trial manager do?
A Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for new drugs, medical devices, or treatments. They ensure that trials are conducted in compliance with regulatory guidelines, company protocols, and ethical standards. Their responsibilities include managing budgets, timelines, and teams, as well as monitoring data quality and safety throughout the study. Clinical Trial Managers also work closely with investigators, sponsors, and regulatory agencies to ensure successful trial outcomes.
What are some common challenges clinical trial managers face when coordinating multi-site studies?
Clinical Trial Managers often encounter challenges such as ensuring consistent protocol implementation across different sites, managing timelines in the face of site-specific delays, and maintaining clear communication among diverse teams. They must also navigate regulatory differences between regions and address unforeseen issues like patient recruitment shortfalls or data discrepancies. Success in this role requires strong organizational skills, adaptability, and proactive problem-solving to keep studies on track and compliant.
More about Clinical Trial Manager jobs
What are the most commonly searched types of Clinical Trial jobs in Riverside, CA? The most popular types of Clinical Trial jobs in Riverside, CA are:
What are popular job titles related to Clinical Trial Manager jobs in Riverside, CA? For Clinical Trial Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Manager jobs in Riverside, CA look for? The top searched job categories for Clinical Trial Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Clinical Trial Manager jobs? Cities near Riverside, CA with the most Clinical Trial Manager job openings:
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
60th of 223 rated it services
Job description
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, 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
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Participate in all required orientation, training, and calibration activities.
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Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.
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Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.
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Complete assigned tasks and rater interactions according to schedule.
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Submit all required documentation accurately and on time.
Required Qualifications
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Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.
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Experience:
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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)
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Minimum 3 years of clinical experience with psychiatric populations.
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Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).
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Experience in CNS trials preferred.
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Skills:
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Strong interpersonal and communication skills for professional interaction at all levels.
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Excellent organizational skills, attention to detail, time management, and problem-solving ability.
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Proficiency with Windows and Microsoft Office applications.
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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.
About IQVIA
Sourced by ZipRecruiter
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.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US