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Ich Gcp Jobs in Silver Spring, MD (NOW HIRING)

The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP. Responsibilities * Under minimal supervision of the project CRA staff ...

The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP. Responsibilities * CRA, Project Manager, etc., independently schedules and ...

The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP. Responsibilities * Under minimal supervision of the project CRA staff ...

The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP. Responsibilities * Under supervision of the project CRA staff oversight lead ...

The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP. Responsibilities * Under the supervision of the project CRA staff oversight ...

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Ensure adherence to FDA regulations, ICH Good Clinical Practice (GCP), and HIPAA guidelines to maintain compliance throughout all trial phases * Review and verify study documentation for accuracy ...

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Ensure adherence to FDA regulations, ICH Good Clinical Practice (GCP), and HIPAA guidelines to maintain compliance throughout all trial phases * Review and verify study documentation for accuracy ...

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Duties: This position requires an experienced clinical research professional with extensive knowledge of ICH-GCP guidelines, FDA regulations, federal research requirements, and clinical trial ...

Ensure site compliance with ICH-GCP, SOPs, and regulations * Maintain up-to-date documentation in CTMS and eTMF systems * Support and track site staff training and maintain compliance records

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Ich Gcp information

See Silver Spring, MD salary details

$51.2K

$120.2K

$181.9K

How much do ich gcp jobs pay per year?

As of Aug 20, 2026, the average yearly pay for ich gcp in Silver Spring, MD is $120,235.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,900.00 and $148,300.00 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 cities near Silver Spring, MD are hiring for Ich Gcp jobs?

Cities near Silver Spring, MD with the most Ich Gcp job openings:

Infographic showing various Ich Gcp job openings in Silver Spring, MD as of August 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 89% In-person, and 11% Hybrid job distribution, with an average salary of $120,235 per year, or $57.8 per hour.

Clinical Trial & Pharmacovigilance Manager

VENESCO LLC

Falls Church, VA • On-site

Full-time

Re-posted 9 days ago


Job description

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