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Ich Gcp Jobs (NOW HIRING)

DM Clinical

Study Manager I (4011)

Sugar Land, 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 ...

DM Clinical

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 ...

DM Clinical

Study Manager I (4078)

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 ...

DM Clinical

Study Manager I (4083)

Phoenix, AZ · 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 ...

DM Clinical

Study Manager I (4012)

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 ...

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Ich Gcp information

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How much do ich gcp jobs pay per year?

As of Aug 12, 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.

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.
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Ich Gcp jobs near you
Infographic showing various Ich Gcp job openings in the United States 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 $116,307 per year, or $55.9 per hour.

Clinical Research Site Director

DM Clinical Research

Tomball, TX

Full-time

Re-posted 5 days ago

Job description

Site Director
The Site Director will ensure study enrollment to meet or exceed Sponsors' expectations, and company goals are achieved on a timely basis. The site director will also ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations and ICH/GCP guidelines and to provide the best quality data to the sponsor.
DUTIES amp; RESPONSIBILITIES
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • 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 supervision and performance of the assigned site staff.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include, but is not limited to, sponsor provided and IRB approved Protocol Training, all relevant Protocol Amendments Training, any study specific Manuals Training as applicable, sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
It is the responsibility of the Site Director to make sure all the relevant training is completed prior to performing any applicable tasks on the assigned study.
  • Working knowledge of the recruitment and relevant cross functional departmental processes for their assigned protocol(s) at their respective site(s).
  • Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate as well as timely follow up on the action items, at their respective sites.
  • Making sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study related documents are utilized and implemented at all times for the assigned protocol(s) at their respective site(s).
  • Working with the Regulatory Team to ensure maintenance of Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
  • Working with the cross functional team(s) and site team(s) to ensure study start readiness on all the aspects and adequate training completed by all the relevant site staff prior to FPFV.
  • Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs and guidance documents.
  • Responsible for providing guidance to the site team on planning and monitoring the conduct of the clinical trials.
  • Accomplishing site objectives by managing staff; facilitating staff training as applicable; communicating job expectations
  • Coaching, counseling and disciplining the employees as applicable.
  • Collaborating with both internal and external cross-functional stakeholders for the successful conduct and management of assigned protocol(s) at their respective sites.
  • To develop, coordinate, and enforce site specific systems, policies, procedures, and productivity standards.
  • Communicating and effective implementation of strategic goals from senior management
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Striving to ensure weekly, monthly and quarterly assigned goals are met for their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Any other matters as assigned by management.

KNOWLEDGE amp; EXPERIENCE
Education:
  • Bachelor’s Degree in a field of Medicine, Science, Behavioral Science, Nursing, or related field required
  • Masters degree preferred
Experience:
  • 5-7 years experience in a managing high growth clinical research sites required
  • 3+ years in multi study management required
  • 3+ years in team management required
Credentials:
  • ACRP- PM, ACRP-CP or equivalent preferred
  • Knowledge and Skills:
  • Excellent communication, organizational and problem-solving skills
  • Strong skills with MS Office and/or Google Suite
  • Expertise in Trial management and ICH-GCP guidelines and FDA Clinical Trial Guidelines
  • Strong attention to detail
  • Strong skills in multi-tasking and delegating tasks
  • Strong People Management skills

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