Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
New
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
New
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
New
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
New
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
New
Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.
New
Clinical Research Associate
Irvine, CA · Remote
$120K - $135K/yr
Track and manage trial documentation, including but not limited to site contracts, investigator ... Perform remote monitoring activities such as source data verification (SDV) and data entry checks ...
Clinical Research Associate
Irvine, CA · Remote
$120K - $135K/yr
Track and manage trial documentation, including but not limited to site contracts, investigator ... Perform remote monitoring activities such as source data verification (SDV) and data entry checks ...
Clinical Research Manager
Irvine, CA · On-site +1
Remote candidates may also be considered. Responsibilities: Under limited supervision and in ... Ensures applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through ...
Clinical Research Manager
Irvine, CA · On-site +1
Remote candidates may also be considered. Responsibilities: Under limited supervision and in ... Ensures applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through ...
Clinical Research Manager
Irvine, CA · On-site +1
Remote candidates may also be considered. Responsibilities: Under limited supervision and in ... Ensures applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through ...
Clinical Research Manager
Irvine, CA · On-site +1
Remote candidates may also be considered. Responsibilities: Under limited supervision and in ... Ensures applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through ...
Associate Director, Clinical Affairs
Irvine, CA · On-site +1
Oversee the Clinical Affairs Trial Management Team during clinical trial cases with physicians ... Remote or field-based positions will have different workplace arrangements which will be indicated ...
Associate Director, Clinical Affairs
Irvine, CA · On-site +1
Oversee the Clinical Affairs Trial Management Team during clinical trial cases with physicians ... Remote or field-based positions will have different workplace arrangements which will be indicated ...
Director, Early Development - Clinical Science
Irvine, CA · On-site +1
$85K - $117K/yr
... trial management experience required * Established leadership track record with evidence of ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Director, Early Development - Clinical Science
Irvine, CA · On-site +1
$85K - $117K/yr
... trial management experience required * Established leadership track record with evidence of ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Director, Early Development - Clinical Science
Irvine, CA · On-site +1
$85K - $117K/yr
... trial management experience required * Established leadership track record with evidence of ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Director, Early Development - Clinical Science
Irvine, CA · On-site +1
$85K - $117K/yr
... trial management experience required * Established leadership track record with evidence of ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...
Clinical Research Leader
Irvine, CA · On-site +1
May serve as the primary contact for clinical trial sites (e.g. site management); * Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...
Clinical Research Leader
Irvine, CA · On-site +1
May serve as the primary contact for clinical trial sites (e.g. site management); * Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...
Clinical Research Leader
Irvine, CA · On-site +1
May serve as the primary contact for clinical trial sites (e.g. site management); * Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...
Clinical Research Leader
Irvine, CA · On-site +1
May serve as the primary contact for clinical trial sites (e.g. site management); * Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...
Clinical Research Leader
Irvine, CA · On-site +1
May serve as the primary contact for clinical trial sites (e.g. site management); * Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...
Clinical Research Leader
Irvine, CA · On-site +1
May serve as the primary contact for clinical trial sites (e.g. site management); * Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual ...
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 ...
Manager, Clinical Affairs (Case Review Board)
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 ...
Manager, Clinical Affairs (Case Review Board)
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 ...
Manager, Clinical Data Research (Remote)
Irvine, CA · On-site +1
$116K - $193K/yr
Remote or Hybrid or Onsite The Manager, Clinical Data Research will oversee the end-to-end collection and processing of clinical trial data. Leads the data management team, enforces regulatory ...
Manager, Clinical Data Research (Remote)
Irvine, CA · On-site +1
$116K - $193K/yr
Remote or Hybrid or Onsite The Manager, Clinical Data Research will oversee the end-to-end collection and processing of clinical trial data. Leads the data management team, enforces regulatory ...
Manager, Clinical Data Research (Remote)
Irvine, CA · On-site +1
$116K - $193K/yr
Remote or Hybrid or Onsite The Manager, Clinical Data Research will oversee the end-to-end collection and processing of clinical trial data. Leads the data management team, enforces regulatory ...
Manager, Clinical Data Research (Remote)
Irvine, CA · On-site +1
$116K - $193K/yr
Remote or Hybrid or Onsite The Manager, Clinical Data Research will oversee the end-to-end collection and processing of clinical trial data. Leads the data management team, enforces regulatory ...
Manager, Clinical Data Research (Remote)
Irvine, CA · On-site +1
$116K - $193K/yr
Remote or Hybrid or Onsite The Manager, Clinical Data Research will oversee the end-to-end collection and processing of clinical trial data. Leads the data management team, enforces regulatory ...
Manager, Clinical Data Research (Remote)
Irvine, CA · On-site +1
$116K - $193K/yr
Remote or Hybrid or Onsite The Manager, Clinical Data Research will oversee the end-to-end collection and processing of clinical trial data. Leads the data management team, enforces regulatory ...
Remote 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 remote clinical trial manager jobs pay per hour?
As of Jul 27, 2026, the average hourly pay for remote 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 is the difference between Remote Clinical Trial Manager vs Remote Clinical Research Associate?
| Aspect | Remote Clinical Trial Manager | Remote Clinical Research Associate |
|---|---|---|
| Credentials | Typically requires a Bachelor's or higher in life sciences, with experience in trial management | Usually holds a Bachelor's in life sciences or related field, with certification in clinical research (e.g., CCRP) |
| Work Environment | Oversees multiple sites, manages trial timelines, budgets, and teams remotely | Monitors trial sites, ensures protocol compliance, and collects data remotely |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Pharmaceutical companies, CROs, clinical research organizations |
The Remote Clinical Trial Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Remote Clinical Research Associate primarily monitors trial sites and data collection. Both roles require clinical research knowledge and often work remotely within the same industry sectors.
What Does a Remote Clinical Trial Manager Do?
Remote clinical trial managers monitor the process of clinical testing from home or another location outside of the office or lab. In this role, you may collaborate with the clinical project manager to create outlines for the trial, research relevant information from existing medical studies, and help ensure the scope of the testing is enough to move the product forward to the next phase. Products may include pharmaceuticals, medical devices, or other forms of medical treatments. Your job duties also involve creating strategies for efficient testing methods, checking that all tests comply with safety standards and current government regulations, documenting results, and supervising research assistants.
What are the key skills and qualifications needed to thrive as a Remote Clinical Trial Manager, and why are they important?
To thrive as a Remote Clinical Trial Manager, you need expertise in clinical research, regulatory compliance, and project management, usually supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and GCP certification are typically required. Exceptional organizational skills, proactive communication, and the ability to lead cross-functional teams remotely set top performers apart. These competencies are crucial for ensuring trial integrity, regulatory adherence, and seamless coordination across distributed teams.
How does a Remote Clinical Trial Manager typically collaborate with on-site study teams and stakeholders?
As a Remote Clinical Trial Manager, you will frequently coordinate with on-site study teams, investigators, and sponsors through virtual meetings, project management platforms, and regular reporting. Effective communication and proactive problem-solving are essential for ensuring trial milestones are met and regulatory requirements are followed, despite not being physically present. You may also oversee remote monitoring visits, address site queries, and facilitate cross-functional collaboration between data management, safety, and regulatory teams. This structure allows for flexibility while maintaining strong oversight and quality standards.
What is a Remote Clinical Trial Manager?
A Remote Clinical Trial Manager is a professional responsible for overseeing the planning, execution, and management of clinical trials from a remote location. They coordinate with various teams, ensure regulatory compliance, monitor trial progress, and manage budgets and timelines, all while working off-site. This role typically involves using digital tools to communicate, track data, and ensure the trial runs smoothly and efficiently. Remote Clinical Trial Managers are essential in facilitating clinical research, especially in decentralized or multi-site studies. They play a key role in ensuring that clinical trials meet both scientific and regulatory standards.
More about Remote Clinical Trial Manager jobs
What are the most commonly searched types of Remote Clinical Trial jobs in Riverside, CA? The most popular types of Remote Clinical Trial jobs in Riverside, CA are:
What are popular job titles related to Remote Clinical Trial Manager jobs in Riverside, CA? For Remote Clinical Trial Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Trial Manager jobs in Riverside, CA look for? The top searched job categories for Remote Clinical Trial Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Remote Clinical Trial Manager jobs? Cities near Riverside, CA with the most Remote Clinical Trial Manager job openings:
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
61st of 230 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 BEHAVE,-AD, E-BEHAVE-AD, BEHAVE-AD-FW, NPIC, ADAS-Cog;CGI-S, C-SSRS)
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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