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Data Integrity Business Analyst (Hybrid , Contract to Hire) at Tech-Nique Partners

Data Integrity Business Analyst (Hybrid , Contract to Hire)

Tech-Nique Partners Queens, NY (Onsite) Full-Time
CB Est Salary: $120K - $120K/Year

Stable Fortune 250 looking to hire immediately.

Data Integrity Business Analyst
W2 Only

Planned to convert within 6 months, must be able to get to Long Island City Office, must be able to convert to full time.

Location: Can be remote but should be EST time - Local to LIC (Queens, NY) required office schedule: Monday/Friday Remote, Tuesday/Wednesday in the office, Thursday is optional to be onsite depending on meeting needs (Remote is ok but they should be local.

Our goal is to transition the consultants to FT employees after 1 yr of service. We do not want their existing location to present an issue w/coming to the office in the future.)

Duration: 6 months - May convert down the line for the right candidate

Max Pay Rate: $74/hr

Must have: Core BA skills

Will be working on Data Integrity projects. Data is GxP data – which typically includes clinical, r&d, manufacturing
Strong preference for GXE experience/Manufacturing experience
Must have some knowledge of experience with GxP data/working on GxP projects
About the project: Data is subject to regulations and must be accurate, This team builds internal policies and procedures around FDA policies.

This person – will continue to make sure we keep technical documentation accurate and updated, will update proper SOPs, etc. Will be updating technical documentation and modifying where needed

• Experience in analyzing business processes for compliance, effectiveness and efficiency.
• Experience in writing technical/compliance process documentation, SOPs and training.
• Strong communication skills for effective stakeholder engagement and consensus building.
• Experience in project management a plus.
• Experience in Electronic Document Management Systems (e.g. OpenText) preferred.
• Knowledge of GxP (Good Manufacturing/Laboratory/Documentation practices).
• Knowledge of FDA Validation and 21 CFR Part 11 a plus but not required.

The primary role of this position is to ensure IT business processes adhere to data integrity principles with effectiveness and efficiency. This position requires analysis of business processes – identifying gaps and remediation options - that will warrant robust processes governed by SOPs/ WKIs. The individual is required to collaborate with Global functions (R&D IT and Global Supply Chain) for an effective Data Integrity (DI) landscape.

The scope includes
• Leading the Process Analysis, Process Documentation and SOP adherence across IT with support to the functions.
• Managing governance of processes, access, SOPs and documentation to ensure compliance.
• Representing IT on the Global Data Integrity Core Team for required regulatory activities.
• Aligning and managing the IT Compliance Training and Awareness program as per compliance initiatives.

The geographic scope is Global supporting all manufacturing & distribution sites - Melville (USA), Lachen/Oevel (Switzerland), Shanghai (China), Toronto (Canada), Seoul (South Korea), Tokyo (Japan), UK (Whitman) and EMEA.

  1. Lead analysis of IT Data Integrity processes to ensure alignment with the overall Enterprise CyberSecurity & Risk corporate objectives
    a. Analyze and document business processes.
    b. Work closely with project managers and key program stakeholders to identify process gaps and remediation options.
    c. Provide guidance on SOP/WKI templates and training to impacted departments to ensure their functional subject matter experts (SMEs) can create the required documentation.
    d. Assist in managing and scheduling ECR’s training and awareness program(s).
    e. Accurate record keeping for all training and training documentation on their respective learning management system (ELC learning center e.g. SumTotal, Sharepoint)
    f. Assist Global DI Lead and R&D Site DI Leads to conduct periodic verification of processes/SOPs/WKIs to ensure they are current and effective.
    2. Collaborating with Corporate functions – Global Supply Chain, Global QA and IT – to ensure SOP and work Instruction standards are aligned cross-functionally.
    3. Provide status updates (monthly/quarterly) at Site level to ensure visibility of process priorities and risks.
    4. Work with Data Integrity IT resources and external vendors to ensure that data integrity controls are being properly maintained in ELC’s central inventory system.

- provided by Dice

Recommended Skills

  • Business Processes
  • Clinical Works
  • Communication
  • Compliance Training
  • Document Management Systems
  • Governance
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