Responsibilities

Implement software and design solutions with Veeva Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Submissions Publishing) at life sciences customers
Lead configuration requirements workshops, design, and document, as well as prototype and deploy solutions
Program and project management, including resource planning, leading and motivating a cross-functional team
Communicate between the project team, customer, and internal stakeholders

Requirements

3+ years in technology implementation services, in life sciences or healthcare
Technical abilities and willingness to 'roll up your sleeves' to design, configure and implement a RIM solution
Ability to collaborate and communicate excellently with diverse stakeholders
Team player with strong organization skills and an ability to work hard in a fast-paced environment
Ability to travel as required by the business

Nice to Have

Consulting experience, working with a major system integrator or software vendor
Knowledge of drug development, Regulatory Affairs, or Regulatory Operations
Experience in life sciences compliance and computer systems validation requirements
Fluency in one or more of the following languages: English, German, French, Spanish, Italian

Compensation

Total compensation: 50,000 - 110,000 EUR. The total compensation range listed here has been provided to comply with local regulations and represents a potential total compensation range for this role. Actual total compensation may vary within the range above or below, depending on experience and location. Total compensation may be composed of variable bonus and/or stock bonus.

Work Arrangement

Remote (Worldwide) — EU, UK

Additional Information

Remote position within EU/UK
Candidate must be in close proximity to an airport
Ability to travel as required by the business
Personality assessment required as part of application process
Work Anywhere company – supports flexibility to work from home or in the office