Consultant - Clinical Operations (Remote - Europe) at Veeva Systems

Copenhagen, Capital, Denmark

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Life SciencesIndustries

Requirements

Experience working in clinical trials with a demonstrated understanding of compliance considerations and processes
AND / OR experience working on implementation projects as a consultant, business, or IT lead for at least one of the following solutions: eTMF, CTMS, Site Connect, Study Training, Study Startup, and Payments
Some understanding of life sciences content management principles
Some understanding of life sciences compliance and computer systems validation requirements
Some content management expertise and/or clinical trials expertise and/or software implementation expertise
EU/UK-based and in close proximity to an airport to meet travel requirements

Responsibilities

Lead life science customers in the rapid configuration and implementation of eTMF, CTMS, Site Connect, Study Training, Study Startup, and Payments solutions
Participate in workshops to discuss requirements with customers
Guide customers toward best design decisions
Document design decisions
Monitor Veeva Vault configuration to ensure it matches the agreed design
Support customers in validation activities and write validation documentation
Deliver onsite or remote training
Submit product enhancement requests based on project experience
Ensure customer success from beginning to end of the engagement lifecycle
Understand customers’ challenges and clinical needs, translate requirements into solution design, and support customers during application validation
For Senior Consultant: Lead and mentor project team members implementing and configuring the designed solution

Skills

eTMF

CTMS

Site Connect

Study Training

Study Startup

Clinical Trials

Software Implementation

Content Management

Solution Design

Customer Training

Configuration

Project Leadership

Veeva Systems

Quality and regulatory software solutions provider

About Veeva Systems

Veeva Systems offers software solutions for quality, regulatory, and advertising claims management, focusing on consumer products and chemical companies. Their cloud-based platform provides visibility and traceability throughout the product journey, ensuring compliance with regulations and accelerating time-to-market. Unlike competitors, Veeva has specialized expertise in both the Life Sciences and Chemical sectors, allowing them to effectively address industry-specific challenges. The company's goal is to help clients efficiently bring safe and compliant products to market.

Pleasanton, CaliforniaHeadquarters

2007Year Founded

$6.8MTotal Funding

IPOCompany Stage

Enterprise Software, Healthcare, Consumer GoodsIndustries

5,001-10,000Employees

Benefits

Parental leave

PTO

Free food

Health, dental, & vision insurance

Gym membership reimbursement

Risks

Manual processes in medtech content management risk compliance issues and market delays.

GenAI features in Vault CRM may face data privacy and security challenges.

Rapid product expansion could lead to integration challenges and customer dissatisfaction.

Differentiation

Veeva Systems specializes in cloud-based software for the life sciences industry.

The company offers a subscription-based model ensuring continuous updates and improvements.

Veeva's Vault CRM Suite connects sales, marketing, and medical for customer-centric engagement.

Upsides

Veeva Compass Patient platform supports patient journey analysis and market sizing.

GenAI features in Vault CRM enhance field productivity with contextual task automation.

Veeva's digital HACCP solution improves safety and efficiency in compliance processes.

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