What You'll Do
- Guide life science customers in the configuration and implementation of Veeva’s Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) to streamline global regulatory processes
- 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 experience working with or for organizations in life sciences or healthcare either as a consultant, business, or IT representative
- 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 act with speed in a complex 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
Perks & Benefits
- Medical, dental, vision, and basic life insurance
- Flexible PTO and company paid holidays
- Retirement programs
- 1% charitable giving program
Compensation
- Base pay: $65,000 - $145,000
- The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.
