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Senior Business Analyst, Data Integration

Fortrea

A distancia

MXN 1,432,000 - 1,791,000

Jornada completa

Ayer
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Descripción de la vacante

A leading CRO is seeking a Senior Business Analyst for Data Integration in Xico, Mexico. This role involves ensuring seamless data flow across systems for Clinical Pharmacology and Global Clinical studies. Responsibilities include data mapping for clinical trials, managing study integrations, and collaborating with various teams to implement solutions. Candidates should have a Bachelor's degree and over 5 years of experience in the life sciences domain, with strong skills in SQL and familiarity with EDC systems such as Rave and Veeva. This is a remote position.

Formación

  • At least 5+ years of experience in the life sciences domain.
  • Extensive knowledge of clinical studies and protocol review for ECRF design.
  • Experience with annotated eCRF and listings mapping.

Responsabilidades

  • Collaborate with study teams to support data mappings.
  • Ensure study solutions maintain a validated state.
  • Manage data issues and provide support for issue resolution.

Conocimientos

SQL development skills
Client-facing experience
Expertise in Rave Webservices and ODM calls
Proficiency in Oracle APEX
Expertise in Excel Power Query

Educación

Bachelor's degree
University / college degree

Herramientas

Rave
Veeva CDMS
Oracle Siebel
ETL workflows
Descripción del empleo
Job Overview

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.

Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

The Senior Business Analyst, Data Integration is pivotal in ensuring the seamless flow of data across critical systems for Clinical Pharmacology and Global Clinical studies.

This role involves designing, programming, and validating mapping data for both streaming and flat files, managing around 250 studies annually.

Each clinical study engages with the analyst to define specific data mappings to ensure that data from study EDC systems flows downstream, enabling critical business processes such as deviation tracking, site payments, study actions, and monitoring reports.

The Senior Business Analyst is responsible for tasks such as mapping, negotiating visit templates, managing repulls, and ensuring direct feeds from EDC systems or flat-file processing into systems like Siebel CTMS, Veeva UCV, and Fortrea proprietary systems.

When issues arise, the role proactively collaborates with system teams to resolve working closely with study project managers and system owners.

Summary of Responsibilities
  • Collaborate with study team to build and support data mappings throughout each study.
  • Map study data for ingestion to downstream systems like CTMS, oversight, monitoring, and grant management tools.
  • Ensure all study solutions maintain a validated state.
Validate integrations connecting EDC to downstream systems
  • Participate in grant payment kick-off and troubleshooting meetings.
  • Lead IT ticket reconciliation for missing data.
  • Lead data issue troubleshooting and re-pulls of data for IT ticket management for missing data.
  • Provide technical support and guidance for issue resolution.
  • Serve as the Subject Matter Expert (SME) for data flow across key Fortrea systems.
  • Collaborate across the organization to implement projects including members from clinical PM, the iGPS Team, DMs, and Xcellerate Teams to ensure correct mappings and ongoing operational support and troubleshooting.
  • Manage the evolution of proprietary processes and technology frameworks for data integrations.
  • Support audits concerning data integrations.
Qualifications (Minimum Required)
  • Bachelor's degree.
  • Extensive knowledge of clinical studies and protocol review for ECRF design.
  • Comprehensive knowledge of EDC front-end and back-end (Rave, Inform, Veeva CDMS, Medrio, etc.).
  • SQL development skills.
  • Veeva Admin certification.
  • Experienced Oracle Siebel Developer.
  • Experience with ETL workflows.
  • Understanding of grant payments workflows and functionality, including grant payment budgets and support.
  • Client-facing experience (internal and external clients).
  • Expertise in Rave Webservices and ODM calls.
  • Experience with annotated eCRF and listings mapping.
  • Proficiency in Oracle APEX for flat file mapping.
  • Expertise in Excel Power Query (Quick Base) customization.
Experience (Minimum Required)
  • University / college degree.
  • At least 5+ years of experience in the life sciences domain.
  • Expertise in metadata mapping.
  • Administration experience with Veeva UCM and Siebel CTMS.
Preferred Qualifications Include
  • Computer programming skills.
  • Demonstrated ability to think creatively and strategically when solving problems and making decisions.

LI-REMOTE

LI-GS1

Fortrea is proud to be an Equal Opportunity Employer

As an EOE / AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions / needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

We encourage all to apply.

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