Full-Time

Technical Curriculum Developer

Pharmacovigilance Software

Confirmed live in the last 24 hours

Veeva Systems

Veeva Systems

5,001-10,000 employees

Quality and regulatory software solutions provider

Enterprise Software
Healthcare
Consumer Goods

Compensation Overview

$65k - $140kAnnually

+ Variable Bonus + Stock Bonus

Mid, Senior

No H1B Sponsorship

Remote in USA

Category
Full-Stack Engineering
Software QA & Testing
Software Engineering
Requirements
  • 3+ years of curriculum development experience, including:
  • Writing administrator or technical learning content for software products with hands-on interactivity
  • Expertise using a variety of tools to create and publish interactive courseware (such as Articulate 360, TechSmith Camtasia, WellSaid, and learning management systems)
  • Excellent written, visual design, and verbal communication skills.
  • Life sciences industry experience, with a strong understanding of Safety (pharmacovigilance, drug safety, regulatory compliance).
  • Consistent track record of accountability in delivering quality projects on time.
  • Ability to both collaborate and work independently in a high-performing, adaptive team.
  • Strong interpersonal skills with the initiative to build collaborative, productive relationships across all lines of business.
  • Demonstrated ability to flexibly take on new challenges and pivot direction if needed
  • Bachelor's degree or years of relevant experience.
Responsibilities
  • Conduct instructional research and task analysis on learner and role context that incorporates a real-world point of view.
  • Apply adult learning theory to the design of engaging training experiences and the development of associated learning assets.
  • Use modern authoring tools to build, deploy, and update courses and supporting materials in the appropriate interactive formats (instructor-led, video, e-learning, hands-on labs, and assessments).
  • Translate complex technical subjects into clear and concise instruction for both functional and technical users.
  • Manage the end-to-end curriculum development process, from initial analysis to design, development, implementation, and evaluation.
  • Work cross-functionally with SMEs and stakeholders to validate learning objectives and technical accuracy and incorporate feedback.
  • Develop a working knowledge of various capabilities of Veeva products and underlying technologies with the aim of becoming an expert in one or more areas.
  • Develop instructionally sound knowledge, skill, and job performance-based assessments.
  • Lead instruction of pilot materials in an internal/external first-teach and in Train-the-Trainer classes.
  • Assist with the creation, configuration, and maintenance of course lab environments and associated data sets required for case studies and lab exercises.
  • Partner with the Project Manager to drive projects with accuracy, transparency, and a commitment to meeting deadlines.
  • Stay current with industry trends, best practices, and new technologies to enhance training delivery methods.
  • Provide solutions and bring innovation to training and enablement strategy and processes.
Desired Qualifications
  • Master's degree in Instructional Design or related field.
  • Certifications in instructional design or curriculum development (e.g., ATD, CPTD).
  • Knowledge of safety data management systems and regulatory frameworks like GxP and ICH guidelines, is a plus.
  • Experience with Veeva products or similar life sciences SaaS platforms is a plus.
  • Shareable work portfolio of previously developed course materials.

Veeva Systems provides specialized software solutions for quality, regulatory, and advertising claims management, primarily targeting consumer products and chemical companies. Their cloud-based software helps clients manage the entire product journey, ensuring that products are high-quality, safe, sustainable, and compliant with regulations. Veeva's solutions offer visibility and traceability from supply chain management to consumer delivery, making it easier for companies to navigate complex regulatory environments. Unlike many competitors, Veeva has a strong focus on the specific needs of the chemical and consumer goods markets, building on its initial success in the Life Sciences sector. The company's goal is to help clients bring products to market more efficiently while maintaining compliance with stringent regulations.

Company Stage

IPO

Total Funding

$6.8M

Headquarters

Pleasanton, California

Founded

2007

Growth & Insights
Headcount

6 month growth

1%

1 year growth

3%

2 year growth

1%
Simplify Jobs

Simplify's Take

What believers are saying

  • Increased adoption of AI-driven analytics enhances Veeva's cloud solutions.
  • The rise of personalized medicine boosts demand for Veeva's patient data solutions.
  • Digital transformation in pharma aligns with Veeva's cloud-based business model.

What critics are saying

  • Emerging cloud-based software providers may erode Veeva's market share.
  • Rapid technological advancements could increase Veeva's R&D costs.
  • Data privacy concerns may impact Veeva's operations and reputation.

What makes Veeva Systems unique

  • Veeva Systems specializes in cloud-based software for the life sciences industry.
  • The company offers end-to-end visibility and traceability in product journeys.
  • Veeva's subscription model ensures continuous updates and improvements for clients.

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Benefits

Parental leave

PTO

Free food

Health, dental, & vision insurance

Gym membership reimbursement