... ICH-GCP and regulatory requirements • Coordinate DSMB activities and safety reviews • Develop and maintain clinical study documentation • Collaborate with regulatory teams on submissions ...
... ICH-GCP and regulatory requirements • Coordinate DSMB activities and safety reviews • Develop and maintain clinical study documentation • Collaborate with regulatory teams on submissions ...
Site Manager (2752)
Albuquerque, NM · On-site
$100K - $120K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Site Manager (2752)
Albuquerque, NM · On-site
$100K - $120K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Site Manager (3768)
Philadelphia, PA · On-site
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Site Manager (3768)
Philadelphia, PA · On-site
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Site Manager (3768)
Philadelphia, PA · On-site
$100K - $120K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Site Manager (3768)
Philadelphia, PA · On-site
$100K - $120K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
OH · Hybrid
Formal ICH GCP training and a working knowledge of ICH GCP Guidelines and other applicable regulatory requirements. * Clear understanding of the requirement to adhere strictly to client ...
Quick apply
OH · Hybrid
Formal ICH GCP training and a working knowledge of ICH GCP Guidelines and other applicable regulatory requirements. * Clear understanding of the requirement to adhere strictly to client ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Study Manager I (3769)
Philadelphia, PA · On-site
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Study Manager I (3769)
Philadelphia, PA · On-site
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Site Manager (3510)
Brookline, MA · On-site
$100K - $120K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Site Manager (3510)
Brookline, MA · On-site
$100K - $120K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Study Manager I (3767)
Houston, TX · On-site
$80K - $96K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Study Manager I (3767)
Houston, TX · On-site
$80K - $96K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Study Manager I (3612)
Melrose Park, IL · On-site
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Study Manager I (3612)
Melrose Park, IL · On-site
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Study Manager I (3612)
Melrose Park, IL · On-site
$80K - $96K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Study Manager I (3612)
Melrose Park, IL · On-site
$80K - $96K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Study Manager I (3767)
Houston, TX · On-site
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Study Manager I (3767)
Houston, TX · On-site
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Confirms site staff have completed required training, including ICH-GCP training, prior to and throughout the study duration. Ensures sites remain inspection ready at all times. * Actively ...
Confirms site staff have completed required training, including ICH-GCP training, prior to and throughout the study duration. Ensures sites remain inspection ready at all times. * Actively ...
Site Manager (3580)
Albuquerque, NM · On-site
$100K - $120K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Site Manager (3580)
Albuquerque, NM · On-site
$100K - $120K/yr
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Responsible for immediate ...
Clinical Research Coordinator III
Chicago, IL · On-site
$25 - $33.25/hr
Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis. * Completing all the relevant training prior to study-start and ...
Clinical Research Coordinator III
Chicago, IL · On-site
$25 - $33.25/hr
Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis. * Completing all the relevant training prior to study-start and ...
Clinical Research Chart QA/Auditor
The Woodlands, TX · On-site
$60 - $100/hr
Conduct internal and external audits of clinical trials, vendors, and systems to ensure compliance with FDA regulations, ICH-GCP, and company SOPs. * Prepare, execute, and document audit plans ...
Quick apply
Clinical Research Chart QA/Auditor
The Woodlands, TX · On-site
$60 - $100/hr
Conduct internal and external audits of clinical trials, vendors, and systems to ensure compliance with FDA regulations, ICH-GCP, and company SOPs. * Prepare, execute, and document audit plans ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s). * Adherence and compliance to ...
Ich Gcp information
See salary details
$49.5K - $61K
3% of jobs
$61K - $72.5K
6% of jobs
$72.5K - $84K
15% of jobs
$84.9K is the 25th percentile. Wages below this are outliers.
$84K - $95.5K
11% of jobs
$95.5K - $107K
11% of jobs
The median wage is $113.5K / yr.
$107K - $118.5K
8% of jobs
$118.5K - $130K
12% of jobs
$139.7K is the 75th percentile. Wages above this are outliers.
$130K - $141.5K
12% of jobs
$141.5K - $153K
12% of jobs
$153K - $164.5K
5% of jobs
$164.5K - $176K
6% of jobs
$49.5K
$116.3K
$176K
How much do ich gcp jobs pay per year?
As of Jun 26, 2026, the average yearly pay for ich gcp in the United States is $116,307.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $143,500.00 per year, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as an ICH GCP (Good Clinical Practice) professional, and why are they important?
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 (Good Clinical Practice) 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?
| Aspect | Ich Gcp | Cloud Engineer |
|---|---|---|
| Certifications | Google Cloud certifications (e.g., Associate Cloud Engineer, Professional Cloud Architect) | Various cloud certifications (AWS, Azure, Google Cloud) |
| Work Environment | Primarily in Google Cloud environments, focusing on GCP tools and services | In diverse cloud platforms, including AWS, Azure, and GCP, depending on employer |
| Industry Usage | Used in companies leveraging Google Cloud Platform for their infrastructure | Common across multiple industries adopting cloud solutions |
| Job Focus | Implementing, managing, and optimizing GCP services | Designing, 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.
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What states have the most Ich Gcp jobs? States with the most job openings for Ich Gcp jobs include:
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Full-time
Posted 14 days ago
Job description
Clinical Trial & Pharmacovigilance Manager
Location: Hybrid
Job Type: Full-Time
Position Overview:
Venesco is seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical trial operations and ensure robust safety surveillance practices.
Requirements
Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and regulatory requirements • Coordinate DSMB activities and safety reviews • Develop and maintain clinical study documentation • Collaborate with regulatory teams on submissions
Minimum Qualifications: • Advanced degree in clinical research, life sciences, or related healthcare field • 8+ years of clinical operations and safety experience • Strong knowledge of ICH-GCP and FDA regulations
Preferred Qualifications: • Experience with Argus or ArisG safety databases • Clinical trial management certification MUST BE A US CITIZEN and US Board certified MD
Location: Hybrid
Job Type: Full-Time
Position Overview:
Venesco is seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical trial operations and ensure robust safety surveillance practices.
Requirements
Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and regulatory requirements • Coordinate DSMB activities and safety reviews • Develop and maintain clinical study documentation • Collaborate with regulatory teams on submissions
Minimum Qualifications: • Advanced degree in clinical research, life sciences, or related healthcare field • 8+ years of clinical operations and safety experience • Strong knowledge of ICH-GCP and FDA regulations
Preferred Qualifications: • Experience with Argus or ArisG safety databases • Clinical trial management certification MUST BE A US CITIZEN and US Board certified MD
About Venesco
Sourced by ZipRecruiter
Company size
51 - 200 Employees
Headquarters location
Chantilly, VA, US
Year founded
2004