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Ich Gcp Jobs in Riverside, CA (NOW HIRING)

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

... ICH-GCP). This position plays a key role in supporting research projects at Diality, combing responsibilities of site management and administrative trial support to ensure smooth and efficient study ...

Diality Inc

Clinical Research Associate

Irvine, CA · On-site

... ICH-GCP). This position plays a key role in supporting research projects at Diality, combing responsibilities of site management and administrative trial support to ensure smooth and efficient study ...

AbbVie

Study Project Manager II

Irvine, CA · On-site

Responsible for operational excellence in all aspects of oversight for clinical studies in compliance with ICH/GCP, Global Regulations, and AbbVie SOPs * Leadership : Demonstrates skills, experience ...

AbbVie

Study Project Manager II

Irvine, CA · On-site

$124K/yr

Responsible for operational excellence in all aspects of oversight for clinical studies in compliance with ICH/GCP, Global Regulations, and AbbVie SOPs * Leadership: Demonstrates skills, experience ...

AbbVie

Study Project Manager II

Irvine, CA · On-site

Responsible for operational excellence in all aspects of oversight for clinical studies in compliance with ICH/GCP, Global Regulations, and AbbVie SOPs * Leadership : Demonstrates skills, experience ...

JenaValve

Specialist, Clinical Safety

Irvine, CA · On-site

$100K/yr

Working knowledge of HIPAA, ICH, GCP, and regulatory requirements related to clinical research. * Experience with cardiovascular or structural heart therapeutic areas is a significant advantage.

Kelly Services

Clinical Research Specialist

Irvine, CA · Hybrid

Participates in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard ...

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All JobsIch Gcp JobsIch Gcp Jobs in Riverside, CA

Ich Gcp information

See Riverside, CA salary details

$51.6K

$121.3K

$183.6K

How much do ich gcp jobs pay per year?

As of Aug 30, 2026, the average yearly pay for ich gcp in Riverside, CA is $121,339.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,700.00 and $149,700.00 per year, depending on experience, location, and employer.

What are ICH GCP guidelines?

ICH GCP, or International Council for Harmonisation Good Clinical Practice, are ethical and scientific quality standards for designing, conducting, recording, and reporting clinical trials involving human subjects. These guidelines ensure that the rights, safety, and well-being of trial participants are protected and that clinical trial data are credible and accurate. ICH GCP is widely accepted internationally and is required by regulatory authorities in many countries for clinical research. Adhering to these guidelines is crucial for anyone involved in clinical trials.

What are the key skills and qualifications needed to thrive as an ICH GCP professional?

To thrive as an ICH GCP professional, you need a solid understanding of clinical research principles, regulatory compliance, and the ethical conduct of clinical trials, typically supported by relevant life sciences degrees and GCP certification. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and regulatory documentation platforms is essential. Attention to detail, strong communication, and organizational skills help ensure protocol adherence and effective teamwork. These competencies are critical for safeguarding participant safety, ensuring data integrity, and meeting regulatory standards in clinical research.

What are some common challenges faced by professionals working in ICH GCP roles, and how can they be addressed?

Professionals in ICH GCP roles often encounter challenges such as ensuring strict regulatory compliance, managing complex documentation, and maintaining clear communication across multi-disciplinary clinical trial teams. Staying updated with evolving global regulations and standards can also be demanding. To address these challenges, it's important to participate in ongoing training, leverage robust project management tools, and foster open lines of communication among stakeholders. Building strong relationships with site staff and regulatory authorities further supports smooth trial operations.

What is the difference between Ich Gcp vs Cloud Engineer?

AspectIch GcpCloud Engineer
CertificationsGoogle Cloud certifications (e.g., Associate Cloud Engineer, Professional Cloud Architect)Various cloud certifications (AWS, Azure, Google Cloud)
Work EnvironmentPrimarily in Google Cloud environments, focusing on GCP tools and servicesIn diverse cloud platforms, including AWS, Azure, and GCP, depending on employer
Industry UsageUsed in companies leveraging Google Cloud Platform for their infrastructureCommon across multiple industries adopting cloud solutions
Job FocusImplementing, managing, and optimizing GCP servicesDesigning, deploying, and maintaining cloud infrastructure across platforms

While both roles involve cloud technology, Ich Gcp specializes in Google Cloud Platform services, whereas a Cloud Engineer may work across multiple cloud providers. The choice depends on the company's cloud strategy and required certifications.

What are popular job titles related to Ich Gcp jobs in Riverside, CA?

For Ich Gcp jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Ich Gcp jobs in Riverside, CA look for?

The top searched job categories for Ich Gcp jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Ich Gcp jobs?

Cities near Riverside, CA with the most Ich Gcp job openings:

Ich Gcp jobs near you
Infographic showing various Ich Gcp job openings in Riverside, CA as of August 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 87% In-person, and 13% Hybrid job distribution, with an average salary of $121,339 per year, or $58.3 per hour.

Research Clinical Director - Psychiatric Pharm Clinical Research

Pacific Neuropsychiatric Specialists Inc

Orange, CA • On-site

$120 - $160/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 16 days ago

Job description

Benefits:
  • Health insurance
  • Paid time off
  • Vision insurance
  • 401(k) matching
  • Bonus based on performance
  • Dental insurance
Pacific Neuropsychiatric Specialists (PNS) is seeking an experienced and dedicated research professional to join our growing team. We are a community-focused, outpatient mental health group serving diverse and underserved populations. Combining the rigor of academic research with direct community impact, we strive to advance the most evidence-based and specialized treatments in psychiatric care—including for Medicaid and Medicare populations. In addition to subspecialized psychiatry services, such as interventional psychiatry, substance use, and child and adolescent psychiatry, we have a robust research division driving cutting-edge innovations in clinical treatments and pharmacologic development. This is an excellent opportunity for a leading researcher who values collaborative research, scientific integrity, and an academically enriching environment.

Job Summary
The Research Clinical Director will serve as a senior research investigator within a growing portfolio of phase II-IV pharmaceutical-sponsored clinical studies. This individual will play a central leadership role across studies spanning multiple psychiatric indications, contributing to the design, execution, and participant oversight of sponsor-initiated trials. The position includes responsibilities managing and overseeing current active trials and potentially serving as the Principal Investigator on future studies, with accountability for regulatory compliance, protocol adherence, and patient safety. This role is well suited for a researcher seeking to lead high-impact psychiatric trials in a dynamic outpatient research setting. An excellent candidate will have 1) scientific credibility, 2) operational excellence in enrollment, retention, data quality, and regulatory compliance, and 3) effectiveness in communication, responsiveness, and consistent delivery across studies.
  • Serve as the site’s primary research authority and accountable investigator for assigned pharmaceutical-sponsored psychiatric trials, with final responsibility for participant safety and protocol integrity.
  • Provide clinical oversight and sign-off on participant eligibility, informed consent, and any protocol deviations or safety events across assigned studies.
  • Liaison research operations director to direct and supervise the study team — including coordinators, sub-investigators, and raters — ensuring protocol compliance and high-quality data across assigned studies.
  • Serve as the primary point of contact for sponsors, CROs, and regulatory agencies; represent the site in investigator meetings, site initiation visits, and monitoring interactions.
  • Exercise clinical judgment on adverse events, serious adverse events (SAEs), and participant discontinuations in coordination with the sponsor medical monitor.
  • Maintain accurate and complete investigator records and ensure assigned studies operate in full compliance with ICH-GCP, FDA, and IRB requirements.
Qualifications
Mandatory Qualifications:
  • Doctorate in a related field (e.g., PhD, PsyD, DSc, or other doctorate in Psychology, Neuroscience, Biology, Chemistry, or Psychopharmacology or related field) from an accredited program
  • No disciplinary action or license restriction
  • Minimum 2 years of clinical research experience, including experience as a PI or sub-PI on pharmaceutical-sponsored trials
  • Demonstrated knowledge of ICH-GCP guidelines, FDA regulations, and IRB/ethics submission processes
  • Supervisory and management experience in managing prior labs
Preferred Qualifications:
  • Current licensure for independent clinical practice (if direct participant assessments or clinical evaluations are required)
Why Join PNS?
  • Shape the future of clinical care through clinical research directly impacting patients
  • Be part of a mission-driven organization committed to serving the underserved and providing exceptional quality care.
  • Work in a supportive interdisciplinary team environment.
  • Competitive compensation and benefits package, including generous matching 401K, medical, dental, vision, and paid time-off.
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