Senior Remedy Database Administrator Job at Chickasaw Nation Industries, Inc (CNI) (Fort Belvoir)

Senior Remedy Database Administrator

The Senior Remedy Database Administrator serves as the senior technical expert f...

Location

United States , Fort Belvoir

Salary:

Not provided

Chickasaw Nation Industries, Inc (CNI)

Expiration Date

Until further notice

Requirements

Must possess an active Top Secret (TS) clearance at the time of proposal submission and be able to attain Sensitive Compartmented Information (SCI) access by the issuance of the contract
Must be a U.S. Citizen
Must be willing to undergo and pass a Counterintelligence (CI) Polygraph
Must possess a MCSA: SQL Server Certification
Must possess a Security+ Certification
Must obtain/retain a government background investigation commensurate with position requirements
Possesses communication skills to effectively interface with military officials, managers, and subordinates
Expertise in Remedy/SQL database planning, architecture, design, and maintenance
Sufficient expertise in the Military Decision Making Process (MDMP), Army Intelligence, and Microsoft Office and SharePoint to accomplish assigned tasks
Results-focused mindset with strong critical thinking and analytical approaches to gather and use multiple sources of information

Job Responsibility

Provides administration and management of Remedy services across development, quality control, pre-production, and production environments
Performs database maintenance activities such as backup/recovery, updates to service packs and patches, and performance optimization
Ensures data recoverability by implementing a schedule of system backups and database archive operations
Performs daily, weekly, and monthly backups of the Remedy Database, its data, and hosts
Conducts periodic restoration tests of backed-up data and supports Disaster Recovery and incident response policies and procedures
Ensures the performance, integrity, and security of databases, monitoring user access and document workflow design
Maintains data standards (including adherence to the Data Protection Act) and writes database documentation, including data standards, procedures, and data dictionary definitions
Controls access permissions and privileges while developing and testing backup and recovery plans
Ensures all major database changes follow the agency Configuration Management Board (CMB) process with met milestones
Provides monthly database reports regarding SQL Server usage, uptime, and capacity to the COR/TTM

What we offer

Medical
Dental
Vision
401(K) Immediate Vesting
Company Life Insurance
Short-Term and Long-Term Disability Insurance
Professional Development Assistance
Legal Aid Assistance Program
Family Planning / Fertility Assistance
Personal Time Off

Fulltime

Senior PostgreSQL Database Administrator

At Paymentology, we’re redefining what’s possible in the payments space. As the ...

Location

Salary:

Not provided

Paymentology

Expiration Date

Until further notice

Requirements

Minimum 7 years of experience in database administration with advanced, hands-on expertise in PostgreSQL
Strong expertise in PostgreSQL architecture, internals, and operational management within enterprise environments
Deep experience in PostgreSQL performance tuning, query optimisation, and schema design at scale
Strong understanding of cloud-native PostgreSQL services, particularly AWS RDS, Aurora, and Redshift
Proficiency in automation and scripting for PostgreSQL operations using Python, Bash, or PowerShell
Advanced knowledge of PostgreSQL backup, replication, high availability, and disaster recovery concepts
Hands-on experience with PostgreSQL ecosystem tools such as pgBadger, pgPool, Slony, and pgBouncer
Strong knowledge of database security, access controls, encryption, and compliance frameworks
Excellent communication and leadership skills with the ability to influence and guide technical teams
A strategic, continuous-improvement mindset with strong ownership and accountability

Job Responsibility

Lead the design and implementation of secure, scalable PostgreSQL database architectures across hybrid and cloud environments including AWS RDS, Aurora, and Redshift
Translate operational and business requirements into optimised PostgreSQL schemas, storage strategies, and replication topologies
Evaluate and integrate emerging PostgreSQL technologies and features to support platform growth, resilience, and long-term sustainability
Oversee the administration of PostgreSQL databases including configuration, upgrades, patching, and lifecycle management
Lead complex PostgreSQL performance tuning initiatives through deep query analysis, execution plan optimisation, and resource allocation
Provide technical guidance to engineers and junior DBAs on PostgreSQL schema design, indexing strategies, and query optimisation best practices
Lead end-to-end PostgreSQL migration projects from on-premise to cloud-native platforms, including lift-and-shift and re-platforming initiatives
Ensure seamless integration of PostgreSQL with cloud infrastructure while maintaining data integrity, availability, and performance
Design and implement solutions supporting elasticity, auto-scaling, and disaster recovery in cloud environments
Design and manage robust PostgreSQL backup, recovery, and disaster recovery strategies to ensure rapid restoration and data protection

Fulltime

Patient Safety Associate II/Patient Safety Specialist - Japanese

Patient Safety Associate II/Patient Safety Specialist - Japanese role at Parexel...

Location

India

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Sound knowledge of drug safety and the drug development process
Knowledge of and ability to interpret and apply global safety regulations
Experience in data analysis and evaluation of safety data
Good presentation skills
Analytical and problem-solving skills
Clear understanding of the regulatory submission process
Proficient in database/literature searches
Excellent interpersonal skills
Excellent verbal / written communication skills
Excellent organizational and prioritization skills

Job Responsibility

Maintaining a good working knowledge of the adverse event safety profile of the assigned drugs, labeling documents, client’s guidelines, and SOPs, and Global drug safety regulations
Maintaining an awareness of global regulatory reporting obligations and organizing work to ensure compliance with internal and regulatory timelines for the adverse event reporting
Assist in development of project specific safety procedures, workflows and templates
Attend/Conduct internal, drug safety and project specific training sessions Completes trainings assigned on internal and client Learning Management System (LMS) as applicable
Preparation for, participation in, and follow up on audits and inspections Maintaining an awareness of the performance metrices measured by the client and striving to remain within established limits
Delegate work as appropriate to Drug Safety Assistants
Liaising and collaborating with the relevant function at the client’s end to facilitate the delivery of high-quality work
Identifies areas of concern and raising the issues with senior management Assist with additional Drug Safety Specialist and/or senior management in project related activities as required
Mentoring new recruits in the team, if required
Archiving the source documents and relevant emails as required

Senior Systems Security Engineer

AnaVation is looking for a Sr. Systems Security Engineer to assist the customer ...

Location

United States , Washington

Salary:

Not provided

AnaVation

Expiration Date

Until further notice

Requirements

5-10 years of experience in information system engineering and configuration management
5 years of experience in control implementation and secure system engineering or design
Excellent communication skills
Hands on experience with: Security monitoring and evaluation, including audits, assessments, and risk management
SIEM tools (e.g., Splunk)
Vulnerability Scanning tools (e.g., Tenable, Nessus)
EDR tools (e.g., Crowdstrike)
Web App Scanning tools (e.g., Burpsuite, Acunetix)
Active Directory
SANs

Job Responsibility

Performing hands-on engineering, administration, and securing of multiple operating systems (e.g., Windows, RHEL, Unix variants), and applying DISA STIGs across diverse vendor technologies, including virtualization platforms (VMWare, Hyper-V), cloud environments (AWS, Azure, Google Cloud), and enterprise applications
Perform system administration tasks to include audit and log management, availability monitoring and remediation, account management and access reviews, and configuration update scheduling and performance
Contribute to the design and development of secure system architectures, ensuring security is integrated through system and network lifecycles
Evaluate, implement, and document security architecture solutions, aligning with compliance requirements and organizational mission needs
Ensure technical compliance with applicable security frameworks, standards, and regulations (e.g., DISA SITGs, NIST 800-53, RMF)
Conducting, configuring, and managing vulnerability scans
Conducting vulnerability remediations, patching, and system hardening
Collaborate with ISSOs, Assessors, System Owners, and other stakeholders to implement security controls
Support security assessments, audits, and accreditation/authorization (ATO) activities
Document security configurations, engineering solutions, and compliance evidence

What we offer

Generous cost sharing for medical insurance for the employee and dependents
100% company paid dental insurance for employees and dependents
100% company paid long-term and short term disability insurance
100% company paid vision insurance for employees and dependents
401k plan with generous match and 100% immediate vesting
Competitive Pay
Generous paid leave and holiday package
Tuition and training reimbursement
Life and AD&D Insurance

Fulltime

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Canada , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Must be fluent in English and in the native language(s) of the country they will work in
Ability to travel 60-80%
Valid driver’s license and passport required
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent

Job Responsibility

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock
Serve as the primary point of contact for assigned investigator sites during study conduct
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel
Provide protocol training to, and address protocol related questions from the investigator site staff
Attend investigator meeting when required (virtual or F2F)
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
Monitor site level adverse events (AEs) and serious adverse events (SAEs)
Submit all required reports, documentation, updates and tracking within required timeframes

What we offer

Patient-focused in everything we do
Supportive and inclusive environment
Career growth and development
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Must be fluent in English and in the native language(s) of the country they will work in
Ability to travel 60-80%
Valid driver’s license and passport required
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent

Job Responsibility

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock
Serve as the primary point of contact for assigned investigator sites during study conduct
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel
Provide protocol training to, and address protocol related questions from the investigator site staff
Attend investigator meeting when required (virtual or F2F)
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
Monitor site level adverse events (AEs) and serious adverse events (SAEs)
Submit all required reports, documentation, updates and tracking within required timeframes

What we offer

Patient-focused in everything we do
Supportive and inclusive environment
Career growth and development
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Turkey

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in English and in the native language(s) of the country they will work in
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Compute Linux Virtualization Engineer

This role has been designed as ‘Hybrid’ with an expectation that you will work o...

Location

India , Bangalore

Salary:

Not provided

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

Deep expertise in HPE Compute platforms (C7000, Synergy, Virtual Connect, ProLiant)
Advanced Linux administration (RHEL, SUSE) including kernel tuning, system hardening, and troubleshooting
Strong virtualization experience in VMware (vSphere, SRM, Horizon), KVM, and Hyper-V
Proficient in VMware infrastructure management: VM lifecycle operations, cluster management, performance monitoring, capacity planning, patching, backup/restore, and snapshot handling
Skilled in analyzing logs (VM-support, HPSreport, SOSreport) and performing root cause analysis
Solid understanding of storage technologies (SAN/NAS/DAS) and protocols (FC, iSCSI, FCoE)
Experience with Red Hat Satellite, SUSE Manager, and patch lifecycle management
Expertise in HA/DR solutions using Serviceguard, Pacemaker, and Linux clustering
Familiarity with networking fundamentals (VLANs, MTU, flow control) and troubleshooting
Strong scripting and automation skills using Bash, Python, and Ansible

Job Responsibility

Acts as a senior technical expert in Compute infrastructure, VMware virtualization, and Linux-based operating systems, providing advanced support and strategic guidance
Leads complex troubleshooting, root cause analysis, and performance tuning across enterprise environments
Provides architectural input and contributes to the design and implementation of infrastructure solutions
Supports transition and transformation initiatives, including migrations, upgrades, and automation efforts
Ensures compliance with ITIL processes and industry best practices
Acts as a technical liaison between internal teams, customers, and third-party vendors
Mentors junior engineers and contributes to knowledge sharing and process improvement
Resolve customer’s issues via the telephone, email or remote sessions
Reproduce issues in-house and responding back in a timely manner
Regular follow ups with customers with recommendations, updates and action plans

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Senior Remedy Database Administrator

Chickasaw Nation Industries, Inc (CNI)

Location:
United States , Fort Belvoir

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 04, 2026

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Senior Remedy Database Administrator

Chickasaw Nation Industries, Inc (CNI)

Location:United States , Fort Belvoir

Category:IT - Administration

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 04, 2026

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United States , Fort Belvoir

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Job Posted:
February 04, 2026