6497 - Business Analyst, Veeva Migration / Business Analyst

Verista, Inc.; United States; Remote; USD 69,000 - 104,000; Full time

Benefits offered by this job

Competitive pay

401(k) plan

Health, Dental, Vision insurance

Paid Time Off

Job summary

Verista is seeking a Business Analyst for Veeva migration within Clinical Operations. You will gather requirements, map data, and support validation and go-live for eTMF migrations to Veeva Vault, collaborating with QA, IT, and vendors.

The role requires 5+ years in regulated life sciences, hands-on Veeva Vault Ops experience, and strong analytical and stakeholder skills. US-based role with competitive compensation.

Qualifications

• 5+ years of experience as a Business Analyst, Functional Analyst, Technical Analyst, or Techno-Functional Analyst in clinical, regulatory or GxP apps.
• Hands-on experience with Veeva Vault Clinical Operations, preferably Veeva eTMF, CTMS, Study Startup, or Site Connect.
• Proven experience supporting eTMF migration projects including document migration, metadata mapping, reconciliation, and validation testing.
• Strong understanding of TMF processes, TMF Reference Model, document completeness, inspection readiness, audit trails, and lifecycle management.
• Experience in regulated life sciences with knowledge of GxP, 21 CFR Part 11, Annex 11, validation, change control, and data integrity.
• Document functional requirements, business processes, data mapping, test cases, traceability.
• Experience supporting UAT, defect management, production readiness, go-live planning, and hypercare.
• Strong analytical, problem-solving, communication, and stakeholder management skills.

Responsibilities

• Partner with Clinical Operations, TMF, Quality, IT, and vendor teams to gather and document requirements for Veeva eTMF migration.
• Support migration planning including scope, mapping, metadata review, classification, audit trails, and readiness activities.
• Translate requirements into specifications, user stories, process flows, test scenarios, and traceability docs.
• Collaborate with technical teams on data extraction, transformation, loading, reconciliation, and verification of eTMF data and metadata.
• Assist with IQ/OQ/UAT planning, test scripts, execution support, defect tracking, and evidence review for GxP systems.
• Support configuration discussions on document types, lifecycles, workflows, roles, permissions, metadata, and TMF alignment.
• Conduct data quality checks and resolve issues like duplicates, missing metadata, mapping mismatches, and document-level discrepancies.
• Coordinate migration dry runs, UAT sampling, production migration verification, and business sign-off.
• Prepare and maintain deliverables: requirements, migration specs, test evidence, defect logs, support plans, and readiness materials.
• Support go-live, hypercare, transition to support, and post-migration issue triage.

Skills

Analytical thinking

Problem-solving

Communication

Stakeholder management

Education

Bachelor's degree in Life Sciences, Computer Science, Information Systems or related field

Tools

Veeva Vault Clinical Operations

Veeva eTMF

Job description

Description

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

The Business Analyst, Veeva Migration will support the planning, execution, validation, and post-go-live stabilization of Veeva Vault eTMF migration initiatives. This role requires a strong understanding of clinical operations, Trial Master File processes, document metadata, data migration activities, and GxP-compliant system delivery. The analyst will work closely with business stakeholders, IT teams, validation partners, migration vendors, and Veeva platform specialists to ensure accurate, compliant, and business-ready migration of eTMF data and documents into Veeva Vault Clinical Operations.

Business Analyst, Veeva Migration Responsibilities:

• Partner with Clinical Operations, TMF, Quality, IT, and vendor teams to gather, analyze, and document business and functional requirements for Veeva eTMF migration activities.
• Support migration planning, including scope definition, source-to-target mapping, metadata review, document classification, audit trail handling, and migration readiness activities.
• Translate business requirements into functional specifications, user stories, process flows, test scenarios, and traceability documentation.
• Collaborate with technical teams to support data extraction, transformation, loading, reconciliation, and verification of eTMF documents and related metadata.
• Assist with validation activities, including IQ/OQ/UAT planning, test script development, execution support, defect tracking, and evidence review for GxP systems.
• Support Veeva Vault configuration discussions related to document types, lifecycles, workflows, roles, permissions, metadata, Expected Document Lists, and TMF Reference Model alignment.
• Conduct data quality checks and support issue resolution related to duplicate records, missing metadata, field mapping inconsistencies, picklist mismatches, and document-level discrepancies.
• Coordinate with business SMEs to support migration dry runs, UAT sampling, production migration verification, and business sign-off.
• Prepare and maintain project deliverables such as requirements documentation, migration specifications, test evidence, defect logs, support plans, and operational readiness materials.
• Support go-live, hypercare, transition to support, and post-migration issue triage to ensure business continuity and user adoption.

Requirements:

• 5+ years of experience as a Business Analyst, Functional Analyst, Technical Analyst, or Techno-Functional Analyst supporting clinical, regulatory, or GxP applications.
• Hands‑on experience with Veeva Vault Clinical Operations, preferably Veeva eTMF, CTMS, Study Startup, or Site Connect.
• Proven experience supporting eTMF migration projects, including document migration, metadata mapping, source-to-target reconciliation, and validation testing.
• Strong understanding of Trial Master File processes, TMF Reference Model, document completeness, inspection readiness, audit trails, and clinical document lifecycle management.
• Experience working in regulated life sciences environments with knowledge of GxP, 21 CFR Part 11, Annex 11, validation, change control, and data integrity expectations.
• Ability to document functional requirements, business process flows, data mapping rules, test cases, traceability matrices, and migration‑related deliverables.
• Experience supporting UAT, defect management, production readiness, go‑live planning, and hypercare support.
• Strong analytical, problem‑solving, communication, and stakeholder management skills.

Preferred:

• Experience migrating content from legacy eTMF systems such as IQVIA eTMF or other clinical document repositories into Veeva Vault.
• Familiarity with Veeva Vault Loader, migration‑center tools, bulk loading processes, and document migration utilities.
• Experience with ALM, Jira, ServiceNow, or similar tools for requirements, testing, change management, and defect tracking.
• Knowledge of clinical trial operations, study‑level data, site documents, monitoring documents, CRO user models, and inspection readiness expectations.
• Bachelor’s degree in Life Sciences, Computer Science, Information Systems, or a related field; equivalent experience may be considered.

_ For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job‑related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future. _

*Verista is an equal opportunity employer.

National (US) Range

$69,300—$104,439 USD

Benefits

Why Choose Verista?

• High growth potential and fast‑paced organization with a people‑focused culture
• Competitive pay plus performance‑based incentive programs
• Company‑paid Life, Short‑Term, and Long‑Term Disability Insurance.
• Medical, Dental & Vision insurances
• FSA, DCARE, Commuter Benefits
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 401(k) Retirement Plan (Employer Matching benefit)
• Paid Time Off (Rollover Option) and Holidays
• As Needed Sick Time
• Tuition Reimbursement
• Team Social Activities (We have fun!)
• Employee Recognition
• Employee Referral Program
• Paid Parental Leave and Bereavement

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For more information about our company, please visit us at Verista.com