Veeva jobs in King of Prussia, PA

Remote

•

Today

an experienced Veeva CRM Lead to provide technical leadership for Veeva CRM and Salesforce-based implementations. experience with Veeva CRM solutions, technical architecture, and application development. Strong expertise in Salesforce Apex, Salesforce Configuration, Veeva Vault SDK, and Veeva Vault Platform. Hands-on experience with Veeva Approved Email, Network, OpenData, Align, Engage, or Events Management. Experience managing large-scale Salesforce/Veeva implementations across the full SDLC.

Contract

Depends on Experience

Veeva CRM developer Remote Location

Remote

•

Today

Job Title : Veeva CRM Lead Must Have TechnicalFunctional Skills 1. Min 5-8 years of Experience in providing solutions and technical architecture for Veeva CRM Suite Applications 2. Experience in full System Development Life Cycle (Proposal, Process Engineering, Design, Development, Testing, Deployment, and Support) Knowledge in Application Design and Development using Salesforce Apex, Salesforce Configurations, Veeva Vault SDK and Veeva Vault Platform configuration. 3. Experience in Veeva Appro

Contract, Third Party

$70 - $70

Veeva RIMS Support SME

Remote

•

13d ago

Veeva RIMS Support SME

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Full-time

Up to $65

Veeva QMS

Remote

•

3d ago

Job title: Veeva QMS Location: Remote Duration: 6 months plus with possible extension Role Descriptions: 1. Veeva QMS 2. Good understanding of Quality processes, including Deviations, CAPA, Lab Investigations, Change Control, Audits, Complaints, and Training. 3. Application Support (Incident, Problem, Change Management) 4. Excellent stakeholder management and communication skills with the ability to interact effectively with business and technical teams. Good-to-Have 1. Work Experience in Pharma

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Contract

Veeva Vault Product Manager

Remote

•

6d ago

Veeva Vault Product Manager Clinical SME | Remote | FTE Location: Remote Employment: FTE Experience: 1022 Years We are hiring an experienced Veeva Vault Product Manager / Clinical Systems SME with strong expertise in Veeva Vault Clinical (CTMS & eTMF) and clinical trial operations. Key Requirements: 812+ years of experience delivering/leading regulated enterprise or clinical systems initiatives Deep hands-on experience with Veeva Vault Clinical CTMS & eTMF Strong understanding of clinical tria

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Full-time

Depends on Experience

Veeva CRM BA

Remote

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10d ago

Veeva CRM BA Remote 12 months contractJD- The Lead Consultant for the Veeva CRM and Vault CRM Platform plays a critical role in developing and delivering tailored solutions that meet client requirements. This position emphasizes the importance of quality and timely execution of consulting projects, fostering strong relationships with clients, and utilizing in-depth technical expertise in the Veeva CRM / Vault CRM Platform to drive successful outcomes. Configuration & Customization:Configure Vaul

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Contract

Depends on Experience

Product Manager - Veeva Vault

Remote

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10d ago

Role: Veeva Vault Product Manager Location: Remote Job Type: FTE/ Full- Time Experience Range: 10- max 22 years Primary Skills: 1. Experience with system integrations (e.g., CTMS eTMF/EDC/Data Lakes & repositories) 2. Experience working with Siebel (CTMS) 3. Experience working with Veeva Managed Services or vendor escalations 4. Familiarity with Agile or DevOps methodologies 5. Knowledge of clinical metrics and reporting tools Required Bachelors degree in Life Sciences, Information Systems, o

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Full-time

Depends on Experience

Clinical Project Manager with RBQM, Veeva, CTMS, eTMF, EDC

Remote

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11d ago

Title: Clinical Project Manager with RBQM & Veeva Foster City, CA or Remote for people who can travel for meetings Experience Range: 10- max 22 years Writeup Skills PM with BA background and experience 6+ years of proven expertise in theclinical domain and operations, including hands-on experience with systems likeCTMS, eTMF, RBQM, and EDC. 8+ years of experience analyzing requirements, documenting findings, and ensuring effective communication and clarification with stakeholders. 6+ years of

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Full-time

Depends on Experience

Veeva Vault Adoption Specialist

Remote

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3d ago

Job Description - Title: Veeva Vault Adoption Specialist Duration: 12+ months Contract Location: Remote MOI: Video Need LinkedIn with profile pic and recent manager references with official email and LinkedIn Must have Veeva, CTMS, ETMF and training experience OBJECTIVES/PURPOSE Work with GDO, R&D and cross-functional stakeholders to collect develop and deploy effective support materials for systems in DSDS ownershipWork with the Business System Owner (BSO) for the system portfolio to identify

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Contract

$40 - $60

Veeva Vault Product Manager

Remote or Hybrid in Foster City, California

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7d ago

HIRING: Veeva Vault Product Manager | Clinical Systems | Full - Time Role Location: Foster City, CA Onsite / Remote Experience: 10+22 Years We are looking for a Veeva Vault Product Manager / Clinical Systems Leader with strong hands-on experience across Veeva Vault Clinical, CTMS, and eTMF in a GxP-regulated pharmaceutical environment. Key Skills Required: Deep experience with Veeva Vault Clinical (CTMS & eTMF) Siebel CTMS experience Experience with CTMS eTMF / EDC / Data Lakes / reposito

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Full-time

Depends on Experience

Veeva RIMS Support SME

Remote

•

13d ago

Veeva RIMS Support SME Location: Remote Duration: 9-12 Month JD Veeva RIMS Support SME

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Contract

Depends on Experience

Head of Commerical Insights

Conshohocken, Pennsylvania

•

Today

Head of Commercial Insights A growing company is seeking a Head of Commercial Insights to lead their analytics department. Experience is the biopharma industry is required. This is a full time direct hire role that will work onsite monthly in the Conshohocken area. Candidates in neighboring states in the mid-atlantic region will be considered. Qualified candidates will have most of the following experience: 12+ years of commercial analytics experience within the pharmaceutical, biotechnology, or

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Full-time

Computer System validation Engineer

Wilmington, Delaware

•

Today

Hi, Title:Computer System validation Engineer Compute System Validation(CSV) with R&D Knowledge Qualification: Bachelor of Science OR Bachelor of Technology OR Bachelor's in Pharmacy Experience: Over 8+ years of overall experience with at least 5 years of experience in Computer System validation for GxP system Knowledge, Experience and Skills: { CORE CSV 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, ITIL, EU Anness 22, ISO 9001, ITIL, Audit/inspection readiness, periodic r

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Full-time, Part-time, Contract, Third Party

Computer System Validation Engineer

Wilmington, Delaware

•

Today

Roles & Responsibilities : 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, ITIL, EU Anness 22, ISO 9001, ITIL, Audit/inspection readiness, periodic reviews, access roster and audit trail reviews, Deviation/CAPA management, SOP/policy compliance processes uthoring of URS/FS, protocols, final reports, validation plan/report High-level understanding of Veeva Vault suits Risk-based testing aligned to CSA fundamentals High-level understanding of Biostatistics, Clinical, Discovery, Med

Full-time

Senior Platform Engineer - CRM Applications

Wilmington, Delaware

•

Today

EMPLOYER: AstraZeneca Pharmaceuticals LP TITLE: Senior Platform Engineer - CRM Applications LOCATION: Wilmington, DE (A hybrid work schedule may be permitted within a commutable distance from the worksite, in accordance with company policies.) HOURS: Full-Time; Mon-Fri (40 hours/week) DUTIES: Plan, analyze, design, configure, test, release, and implement Customer Relationship Management ("CRM") Platforms. Work with third-party suppliers and provide recommendations on enhancements, monitor pe

Full-time

Regulatory Operations Project Manager, Global Submissions Planning/ Management

Remote or Almont, Colorado

•

Today

Description: Remote Our client seeks a Regulatory Operations Project Manager to lead global eCTD submissions planning and management for high profile molecules and lifecycle management. The role focuses on operational submission content planning for Modules 1-5, coordination of global submissions and urgent authority requests, and partnership across geographies to ensure compliance with evolving eCTD requirements. The position reports to the Head of Regulatory Operations Clinical and Publishin

Contract

Senior Data Manager, CRO Oversight, Early Phase Studies

Remote or Almont, Colorado

•

Today

Description: Remote Our client is seeking a Senior Data Manager to provide operational support across multiple early-stage clinical studies in a wide variety of therapeutic areas. This individual will partner with cross-functional study teams and external CROs to ensure the timely delivery of high-quality clinical data that supports informed decision-making throughout Phase 1 first-in-human and Phase 1b/2 patient studies. This is a highly operational role requiring the ability to manage multip

Contract

Business Analyst, AI & Enterprise Data Products with Pharma domain exp + Google Cloud Platform environment exp

Remote

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9d ago

Business Analyst, AI & Enterprise Data Products with Pharma domain exp + Google Cloud Platform environment exp Duration: 12+ Months Location: Remote Work Authorization: USC Position Summary We are seeking a Business Analyst to define requirements for an AI-driven application serving internal business functions across Quality / Manufacturing / Clinical / Regulatory / Commercial. The application sits on top of a substantial data layer, drawing from multiple enterprise source systems, and uses m

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Contract

60 - 65

Clinical Data Ingestion Senior Manager

Remote

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30+d ago

Job Title: Clinical Data Ingestion Senior Manager Location: Poland/Hungary/Mexico Job Type: Full-Time Job Overview: Objective / Purpose: The Clinical Data Ingestion Senior Manager is responsible for ingesting, validating, and operationalizing clinical data feeds into clinical data review platforms (e.g., Veeva CDB, Elluminate, JReview) to enable efficient, high-quality clinical data review. This role focuses on strong ingestion principles, building and scaling reusable ingestion frameworks, and

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Full-time, Third Party

Depends on Experience

Regulatory Affairs Specialist Small Molecule

Remote

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7d ago

Job Title: Clinical Regulatory Affairs Specialist Small Molecule Location: Remote We are seeking a Clinical Regulatory Affairs Specialist with 9+ years of experience supporting small molecule clinical development programs.Key Requirements:Strong experience in Clinical Regulatory AffairsHands-on experience with Veeva Vault TMF or similar.Experience with IND, CTA, and NDA submissionsKnowledge of ICH-Google Cloud Platform, FDA, EMA, and global regulatory requirementsExperience supporting clinical

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Contract, Third Party

Depends on Experience

Veeva jobs in King of Prussia, PA, USA