Regulatory Intelligence Analyst

Veeva Systems • Toronto, Ontario, Canada • 1d ago

The Role

What You'll Do

Identify regulatory requirements related to the product and implement best practices for monitoring, interpreting, and communicating changes to internal teams
Proactively monitor, investigate, interpret, and communicate changes to regulatory requirements that may impact the current product
Proactively monitor the global regulatory landscape for upcoming health authority initiatives or projects that may impact the product in the future
Work directly with product management to translate regulatory requirements into Veeva's framework for use within our suite of applications
Translate long and complex regulatory guidance into clear, concise, and easy-to-understand information for different internal teams
Work with a team of Regulatory Intelligence Analysts to continually improve the processes and tools used for collecting, documenting, managing, and communicating regulatory intelligence

Requirements

3+ years experience in one or more of the following industries and roles: commercial software (e.g., product management, solutions consulting, customer success), quality assurance, CMC, clinical development (e.g., clinical operations), pharmacovigilance, regulatory affairs, or regulatory operations in the life sciences industry
Working knowledge of regulatory processes and procedures in at least one regulated sector of the life sciences industry (e.g., regulatory, clinical, commercial, quality, pharmacovigilance, CMC)
Excellent research, analysis, and interpretation skills, with a strong ability to discern high-quality source information from low
Excellent verbal and written communication and presentation skills, with the ability to translate complex regulatory requirements into easy-to-understand information for multiple internal teams
Highly organized with exceptional attention to detail
Self-starter, driven, and able to work independently as well as part of a team
Excellent working skills with office software (e.g., MS Office, Google Suite)
Willingness to travel occasionally to Veeva offices
Located on the east coast of the United States or Canada

Nice to Have

Experience working with Veeva's products and processes
Experience working in a dedicated regulatory intelligence role in the life sciences industry
Experience working with or for a health authority (e.g., Health Canada, FDA, EMA)
Additional experience in other regulated product areas (e.g., clinical in addition to regulatory, or quality in addition to CMC)

Perks \& Benefits

Medical, dental, vision, and basic life insurance
PTO and company-paid holidays
Retirement programs
1% charitable giving program

Compensation

Base pay: $80,000 - $120,000 CAD
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.

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