2,873 Data Integrity jobs in India

Who are Inchcape?

At Inchcape Shipping Services, our vision is to create a connected world where customers can trade successfully and make informed decisions in every port, everywhere. We achieve this by combining our worldwide infrastructure with local expertise, through our global network of more than 250 proprietary offices and a team of over 3,000 dedicated professionals. Our diverse customer base includes owners and charterers in the oil, cruise, container, and bulk commodity sectors, as well as naval, government, and intergovernmental organizations.

We have an ambitious growth model, and a career here is certainly going to be a rewarding one that will allow you to bring your skills

& experience. We embrace change and are open to new thinking and pushing for positive change in our industry.

Job Purpose
Reporting to Supervisor, the role shall be primarily responsible to input the data into System with 100% accuracy as well as engage with local agents for timely submissions of cargo documents.

• Identify call with missing events updated in system and action accordingly.
• Identify incorrect event updates (illogical sequence of dates, missing dates, incorrect sequential nature of events) in system and action accordingly.
• Chase LPAs for correct and missing events.
• Maintain communication links and coordination with LPAs for any additional information and data.
• Ensure the cargo documents are collected and uploaded in system (especially the SOF).
• Supporting the AMPS & Ops Support manager in delivery of the Medium to long term goals.
• Normal working hours but if business demands then Shift working

The post holder will carry out any other duties as are within the scope and purpose of the job as requested by the Line Manager and ensure full utilization of all ISS systems according to Standard Operating Procedures.

Duties and Responsibilities

Data Audit, Optic Updates as per KPIs

• Ensure correct information in operational files is checked and updated.
• Team member to promptly address within designated KPIs the Service Requests from stakeholders (internal / external)
• Audit event data and ensure sanitary checks are in place to identify errors and mismatch in data.
• Resolve any issues arising from day to day operations, discuss your proposed solutions with Supervisor/Line Manager as required.
• Ensure all queries and requests handled that may arise from the Clients, Masters, Agents, and internal stakeholders.
• To promptly address within designated KPIs the Service Requests from stakeholders (internal / external)
• Deliver and Demonstrate (via reports) that internal KPIs of Validations and event audits are successfully carried out for Optic calls.
• Taking the decision to conduct a response to above yourself when the issue might be sensitive and require extra care.
• Open to work on adhoc requests as per business requirements.
• Share ideas and areas of concerns and findings of the tasks handled in team meetings for future actions plans.
• Ensure necessary steps are taken to chase and rectify missing/incorrect events in system.
• Smooth communication with local agent and Hub Operations for collections of cargo documents.
• Flexible to work in shifts and schedules in order to manage daily/weekly volumes.
• Bring innovative ideas in developing the processes.
• Prepare reports as required by Line Manager The post holder will carry out any other duties as are within the scope and purpose of the job as requested by the Line Manager and ensure full utilization of all ISS systems according to Standard Operating Procedures

Teamwork

• To proactively collaborate with and support colleagues by adopting the spirit of teamwork.
• To inform colleagues promptly of any emails, tasks or issues that require immediate attention to enable them to meet the expectations of internal and external customers.
• To work with all colleagues in a friendly, business focused, proactive and cooperative manner.

QHSSE – Quality, Health, Safety, Security and Environment (mandatory requirements):

• Accountable for ensuring that an appropriate assessment of Health, Safety, Security and Environment (HSSE) risk is included as part of work planning.
• Accountable for implementation and monitoring of actions to mitigate risk and enhance controls within area of responsibility to ensure the HSSE of both the job holder and other persons who may be affected by acts carried out or failed to be carried out by the job holder.
• Ensure full compliance with and implementation of, the ISS HSSE Management System.
• Ensure that appropriate resources are allocated to control HSSE risk.
• Accountable for ensuring that clear, appropriate and timely communication channels are put in place to report and manage HSSE risk.

Knowledge

• Proficient with Microsoft Office (Word, Excel, PowerPoint)
• Basic understanding of Shipping industry and shipping terms (would be added advantage)
• Knowledge on Shipping operations, B/L and Manifest.

Skills

• Good communication skills: Verbal & Written.
• Good motivational skills
• Honest, transparent, and trustworthy
• Proactive, dynamic, Flexible and innovative
• Culturally aware and diplomatic

Experience

• Exposure to shipping will be added advantage.
• Diploma in Shipping Operations.
• Working knowledge of Port and cargo operations

Core:

• Customer Focus
• Ethics and Integrity
• Organizational Commitment
• Health & Safety Compliance

Key:

• Teamwork
• Planning and Delivery
• Business Administration
• Adaptability and Change
• Managing Work Processes
• Initiative
• Quality Focus
• Data Analysis

Management:

• Business Acumen
• Managing Performance
• Leadership
• Shares the Vision
• Decision Making

This role involves overseeing the conduct of thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies in collaboration with functional team leads and project managers.

The successful candidate will be responsible for performing centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks, ensuring data accuracy and compliance.

Supporting monthly quality management meetings by reviewing study data, documenting findings, action plans, and coordinating data cleaning activities to support study deliverables is also a key aspect of this position.

In addition, the ideal candidate will ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.

• Conduct thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies in collaboration with functional team leads and project managers.
• Perform centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks, ensuring data accuracy and compliance.
• Support monthly quality management meetings by reviewing study data, documenting findings, action plans, and coordinating data cleaning activities to support study deliverables.
• Ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.

• Bachelor's Degree in a relevant field (life sciences, statistics, data management, clinical operations) or equivalent combination of education, training, and experience.
• Minimum 2 years experience in clinical monitoring, clinical trial management or equivalent.
• Working knowledge of ICH GCP guidelines and the clinical development process.

Job Title: Central Monitor II

Job Summary:

The Central Monitor II will ensure the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.

This position involves leading the development of Risk-Based Quality Management (RBQM) plans, conducting study risk assessments, identifying study Key Risk Indicators (KRIs), performing ongoing centralized statistical monitoring, remote centralized data review, and facilitating monthly RBQM meetings.

The Central Monitor II works independently and manages report review and issue escalation for complex studies and portfolios of work.

Responsibilities:

• Study Risk Assessment: Conduct thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies in consultation with functional team leads and Project Managers.
• Centralized Statistical Monitoring: Perform centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks, ensuring data accuracy and compliance.
• RBQM Meetings: Support monthly RBQM meetings by reviewing study data, documenting findings, action plans, and coordinating data cleaning activities to support study deliverables.
• Data Quality Assurance: Ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.
• Collaboration: Work closely with clinical operations, data management, biostatistics, and other departments to support proactive oversight and management and data cleaning for studies.
• Reporting: Prepare detailed reports and presentations on monitoring activities, findings, and recommendations for sponsors and study teams.
• Operational Insights: Oversee operational study metrics, including data entry trends, SDV backlog, site health trending, and proactively communicate issues to study team members to drive towards resolution and proactive remediation.

Requirements:

• Strong knowledge of clinical trial data management principles and practices.
• Experience with Risk-Based Quality Management (RBQM) concepts and methodologies.
• Excellent analytical, problem-solving, and communication skills.
• Ability to work independently and manage multiple priorities.

What We Offer:

• A dynamic and collaborative work environment.
• Opportunities for professional growth and development.
• A competitive compensation package.

Central Monitoring Specialist Role Overview

We are seeking a highly skilled and experienced Central Monitoring Specialist to play a key role in ensuring the quality and integrity of clinical trial data.

1. Risk Assessment and Mitigation : Conduct thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies in collaboration with functional team leads and project managers.
2. Data Quality and Compliance : Perform centralized statistical monitoring and data analysis on study data to detect anomalies, trends, and potential risks, ensuring data accuracy and compliance.
3. RBQM Support : Support monthly Risk-Based Quality Management (RBQM) meetings by reviewing study data, documenting findings, action plans, and coordinating data cleaning activities to support study deliverables.
4. Proactive Monitoring : Ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.
5. Collaboration and Communication : Work closely with clinical operations, data management, biostatistics, and other departments to support proactive oversight and management and data cleaning for studies.
6. Reporting and Presentations : Prepare detailed reports and presentations on monitoring activities, findings, and recommendations for sponsors and study teams.
7. Operational Metrics Oversight : Oversee operational study metrics, including data entry trends, SDV backlog, site health trending, and proactively communicate issues to study team members to drive towards resolution and proactive remediation.

This role requires a Bachelor's Degree in a relevant field or relevant/equivalent combination of education, training, and experience. A minimum of 2 years' experience in clinical monitoring, clinical trial management, or equivalent is also required.

We're seeking a seasoned expert to oversee data integrity within our manufacturing control systems.

• Validate and authenticate data sets from SCADA, PLC systems to ensure they're reliable and trustworthy.
• Identify gaps, missing values, and inconsistencies in structured and semi-structured data.

The successful candidate will work closely with manufacturing system owners and business stakeholders to resolve data-related issues.

• 6–10 years' experience as a Data Analyst/Engineer in manufacturing or industrial data environments.
• Strong understanding of SCADA, PLC, and manufacturing control systems data.
• Experience with data lakes and relational database systems.

We are seeking a detail-oriented and technically skilled professional to support and enhance our enterprise systems. This role will focus on ensuring data integrity across ERP platforms, collaborating with cross-functional teams to support business operations.

• This position requires a strong understanding of ERP Item Master concepts, including attributes and categories.
• Familiarity with Product Data Hub (PDH), PLM, or MDM systems is beneficial.

The ideal candidate will have experience in ERP Item Master Data and excellent problem-solving, communication, and documentation skills.

• Collaborate with business users, supply chain, manufacturing, and IT teams to gather requirements and translate them into technical solutions.
• Analyze and troubleshoot item-related issues across ERP systems and integrated platforms.
• Support data migration, cleansing, and enrichment activities during ERP upgrades or implementations.
• Participate in UAT, system testing, and production deployments related to item data changes.
• Work closely with integration teams to ensure seamless data flow between authoring systems and transactional systems.

Benefits:

This role offers a competitive compensation package, commensurate with experience and qualifications.

This is a challenging role that requires a highly skilled and experienced professional to play a key part in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.

• Leading the development of Risk-Based Quality Management (RBQM) plans
• Conducting study risk assessments, identifying potential issues and developing mitigation strategies
• Performing ongoing centralized statistical monitoring and remote centralized data review
• Facilitating monthly RBQM meetings
• Ensuring the highest standards of data quality and integrity through proactive monitoring and timely interventions

• Bachelor's Degree in a relevant field or relevant/equivalent combination of education, training, and experience
• Minimum 2 years experience in clinical monitoring, clinical trial management, or equivalent
• Working knowledge of ICH GCP guidelines and the clinical development process

• Statistical analysis and data monitoring
• Risk assessment and mitigation
• Report writing and presentation
• Collaboration and teamwork

• CRO experience as a Central Monitor

The Central Monitor II plays a vital role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.

This position involves leading the development of Quality Management Plans , conducting study risk assessments, identifying key risk indicators, performing ongoing centralized statistical monitoring, remote data review, and facilitating regular Risk-Based Quality Meetings .

Key responsibilities include study risk assessment, centralized statistical monitoring, quality meetings, data assurance, collaboration with teams, reporting, and operational insights.

Essential qualifications include a Bachelor's Degree in a relevant field, minimum 2 years experience in clinical monitoring, working knowledge of ICH GCP guidelines , excellent communication skills, organizational skills, and proficiency in statistical analysis and data monitoring tools.

• Collaborate with business users, supply chain, manufacturing, and IT teams to gather requirements and translate them into technical solutions.
• Analyze and troubleshoot item-related issues across ERP systems and integrated platforms (e.g., Product Data Hub, PLM).
• Support data migration, cleansing, and enrichment activities during ERP upgrades or implementations.
• Participate in UAT, system testing, and production deployments related to item data changes.
• Work closely with integration teams to ensure seamless data flow between authoring systems and transactional systems.

• Bachelor's degree in Computer Science, Information Systems, Engineering, or related field.
• 5+ years of experience as a Technical Analyst or similar role, with hands-on ERP experience.
• Strong understanding of ERP Item Master concepts, including attributes and categories.
• Experience with Oracle R12, SAP, or other ERP platforms.
• Familiarity with Product Data Hub (PDH), PLM, or MDM systems is a plus.

This role requires excellent problem-solving, communication, and documentation skills. If you have a strong technical background and can thrive in a collaborative environment, we encourage you to apply.