Systems Designer / Analyst II - # 26-17800

US Tech Solutions, Inc.
  • Princeton, NJ
  • $40–$41.50 Per Hour
  • Quick Apply
20 days ago

Job Description

Contract Duration: 1 Year extended for 2 nd year

Purpose:
Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Clinical Data Strategy Organization.

Responsibilities:
  • Actively participates in the development of common data standards and ensures systems designs comply with the standards, as well as with associated protocol requirements. Ensures that the design team utilizes standards
  • Establishes and maintains methodology used by the team to design and develop clinical trial systems, benchmarking against industry standards. Ensures that systems are specified to optimize functionality, end user experience, and data flow. Ensures that the design team meets these expectations
  • Ensures that TA- and program-level consistency is achieved by the design team
  • Accountable for the on-time design and delivery of new clinical systems, integration between systems, as well as any required changes to clinical systems (e.g., EDC, IRT, ePRO). Utilizes project management tools to track study progress and plan work. Anticipates and identifies issues that could affect timelines or quality and develops options and solutions
  • Interacts with and influences CDO and cross-functional team members to achieve program and study objectives. Ensures that assigned work product is synchronized with upstream and downstream dependencies
  • Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, Client Standard Operating Procedures (SOPs), and functional quality standards. Stays abreast of new and/or evolving local regulations, guidelines and policies related to clinical development
  • Responsible for coaching and mentoring members of the team, as well as contributing to their skill development
  • Leads CDO and cross-functional innovation and process improvement initiatives
Qualifications
  • Bachelor’s degree in business, management information systems, computer science, life sciences or equivalent. Masters preferred.
  • Must have 7+ years of hands-on technical Study build in EDC. Experience with technical study build in Medidata RAVE is required. Veeva EDC technical study build experience is a plus.
  • In-depth knowledge of clinical trial processes.
  • In-depth knowledge of CDASH (Required) and SDTM.
  • Demonstrated performance as a key contributor to initiatives and advancement of the organization.
  • Demonstrated ability to influence others without direct authority. Demonstrated ability to successfully coach / mentor in a matrixed environment. Demonstrated effective communication skills and analytical skills.
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.

US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

AI Statement:
By applying, you acknowledge that AI-assisted tools may be used during hiring.

Numbers & Facts

LocationPrinceton, NJ
Salary$40–$41.50 Per Hour

Skills

  • Analysis Skillsunmatched
  • Artificial Intelligence (AI)unmatched
  • Benchmarkingunmatched
  • Biologyunmatched
  • Business Solutionsunmatched
  • Clinical Dataunmatched
  • Clinical Information Systemsunmatched
  • Clinical Trialunmatched
  • Coachingunmatched
  • Communication Skillsunmatched
  • Computer Scienceunmatched
  • Cross-Functionalunmatched
  • Data Scienceunmatched
  • Drug Developmentunmatched
  • Electronic Data Capture (EDC)unmatched
  • Federal Laws and Regulationsunmatched
  • GCP (Good Clinical Practices)unmatched
  • ICH Regulationsunmatched
  • Identify Issuesunmatched
  • Industry Standardsunmatched
  • Maintain Complianceunmatched
  • Management of Information Systems/Technology (MIS)unmatched
  • Mentoringunmatched
  • Process Improvementunmatched
  • Project Management Softwareunmatched
  • Quality Metricsunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Standards Developmentunmatched
  • System Integration (SI)unmatched
  • Systems Analysisunmatched
  • Time Managementunmatched
  • User Interface/Experience (UI/UX)unmatched

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