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Ich Gcp Jobs in Riverside, CA (NOW HIRING)

City of Hope

Clinical Study Coord

Irvine, CA · On-site

Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies. * Follow and execute clinical trial protocols and procedures. * Coordinate participant recruitment ...

JenaValve

Associate, Clinical Research

Irvine, CA · On-site

$75K/yr

The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable ... ICH guidelines. * Very organized and able to pay close attention to detail. * Team player with a ...

JenaValve

Associate, Clinical Research

Irvine, CA · On-site

$75K/yr

The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable ... ICH guidelines. * Very organized and able to pay close attention to detail. * Team player with a ...

Flourish Research

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

A clear understanding of ICH, FDA, and GCP regulations * Impeccable organizational skills and attention to detail * Excellent communication and interpersonal skills to effectively interact with the ...

Flourish Research

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

A clear understanding of ICH, FDA, and GCP regulations * Impeccable organizational skills and attention to detail * Excellent communication and interpersonal skills to effectively interact with the ...

Flourish Research

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

A clear understanding of ICH, FDA, and GCP regulations * Impeccable organizational skills and attention to detail * Excellent communication and interpersonal skills to effectively interact with the ...

JenaValve

Senior Associate, Clinical Research

Irvine, CA · On-site

$95K/yr

The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable ... ICH guidelines. * Very organized and able to pay close attention to detail. * Team player with a ...

JenaValve

Manager, Clinical Research Affairs

Irvine, CA · On-site

$145K/yr

In-depth understanding of Good Clinical Practice (GCP) and applicable regulations, including ISO 14155, ICH Guidelines, and relevant medical device directives/regulations. * Demonstrated experience ...

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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 10, 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.

How to become ICH GCP certified?

To become ICH GCP certified, individuals typically complete a recognized GCP training course that covers clinical trial regulations, ethical standards, and Good Clinical Practice guidelines. After training, some certifications require passing an exam to demonstrate understanding of GCP principles, which are essential for roles in clinical research and trial management.

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 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 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.

Clinical Study Coord

City of Hope

Irvine, CA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

City Of Hope rating

8.4

Company rating: 8.4 out of 10

Based on 89 frontline employees who took The Breakroom Quiz

24th of 887 rated healthcare providers

Job description

Clinical Study Coordinator 
Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. 
Orange County Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials. Under the supervision of the Director, Clinical Research, this patient-facing role involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations, strong organizational skills, and the ability to collaborate with investigators and clinical staff in a fast-paced environment.
As a successful candidate, you will: 
  • Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies.
  • Follow and execute clinical trial protocols and procedures.
  • Coordinate participant recruitment, informed consent, and care.
  • Communicate with participants, investigators, and sponsors to ensure clear understanding and compliance.
  • Monitor and document participant eligibility, safety, and protocol adherence, and report adverse events promptly.
  • Pursue continuous education and training opportunities, staying updated with the latest clinical research information, and maintain necessary certifications and licensure.
 
Qualifications - External
 
Qualifications - External
 
Qualifications - External

Your qualifications should include: 

  • Bachelor's degree in Science, Health or related field from an accredited university; 3 additional years of experience plus the minimum experience requirement may substitute for minimum education.
  • Minimum of 2 years research or relevant clinical experience
  • ACRP or SOCRA certification within 1 year of employment
  • International Air Transport Association (IATA) within 1 month of employment
  • Good Clinical Practice (GCP) within 1 month of employment
  • Human Subjects Protection (HSP) within 1 month of employment
  • Basic Life Support (BLS) within 1 month of employment

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.  To learn more about our commitment to diversity, equity, and inclusion, please click here.

To learn more about our Comprehensive Benefits, please CLICK HERE.

What City Of Hope employees say

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About City of Hope

Sourced by ZipRecruiter

City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases. Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hopes translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hopes specialized cancer expertise. City of Hope is ranked among the nations Best Hospitals in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.

Industry

Hospitals

Company size

1,001 - 5,000 Employees

Headquarters location

Duarte, CA, US

Year founded

1913

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