السعودية
GCP Subject Matter Expert
DXC Technology
- Industry Type
- Oil, Gas, Petroleum
- Functional Area
- IT Information Technology Industry Oil, Gas, Petroleum
- Nationality
- Any
- Keywords
- Google Cloud Platform GCP Solutions Design Cloud Migration Strategies Infrastructure as Code IaC Development Terraform or Deployment Manager Profi
Job Description
DXC Technology is seeking a GCP Subject Matter Expert in Riyadh, Saudi Arabia, to design and implement secure and scalable Google Cloud Platform solutions. The role includes leading cloud migration strategies and developing Infrastructure as Code using Terraform or Deployment Manager.
- Position
- GCP Subject Matter Expert
- Company
- DXC Technology
- Location
- Riyadh, Saudi Arabia
- Industry
- Oil, Gas, Petroleum
- Experience
- 1 to 20 years
Responsibilities
- Design and implement secure, scalable, and cost-effective Google Cloud Platform solutions for enterprise and retail IT environments.
- Lead cloud migration strategies, including planning and executing workload transitions to GCP.
- Develop and maintain Infrastructure as Code using Terraform or Deployment Manager.
- Integrate Google Cloud services to enhance system functionality.
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About the role: GCP Subject Matter Expert
General information about this type of role, not from the employer. The employer's actual requirements may differ, so always check the job details above.
A GCP (Good Clinical Practice) Subject Matter Expert ensures that clinical trials and research projects comply with established ethical and scientific quality standards. They typically work in the pharmaceutical, oil, gas, or petroleum industries where clinical or safety studies are conducted, often collaborating with research teams and regulatory bodies.
What this role usually involves
- Provide expert guidance on Good Clinical Practice standards and regulations.
- Review and develop clinical trial protocols and related documentation.
- Ensure compliance with ethical guidelines and regulatory requirements during studies.
- Train and support staff on GCP principles and procedures.
- Monitor ongoing clinical studies for adherence to quality standards.
- Advise on risk management and quality assurance in clinical research.
Skills employers usually look for
- Strong knowledge of Good Clinical Practice guidelines and regulatory frameworks.
- Attention to detail and analytical skills for reviewing study documents.
- Effective communication and training abilities.
- Problem-solving skills related to compliance issues.
- Ability to work collaboratively with multidisciplinary teams.
- Organizational skills to manage multiple projects and deadlines.
Usual qualifications
- A degree in life sciences, pharmacy, medicine, or a related field.
- Specialized training or certification in Good Clinical Practice.
- Experience in clinical research or quality assurance roles.
- Familiarity with regulatory requirements in clinical trials.
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