Regulatory Intelligence Analyst at Veeva Systems Radnor, PA

Veeva Systems; Radnor (Delaware County); On-site; USD 75,000 - 115,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

Flexible PTO and holidays

Retirement programs

1% charitable giving program

Job summary

Veeva Systems, based on the East Coast with offices nationwide, seeks a Regulatory Intelligence Analyst in Radnor, PA. You will monitor regulatory guidance, translate requirements, and inform Product Management and internal teams to keep products compliant across global health authorities.

The role emphasizes research, interpretation, clear communication, and collaboration within a supportive team. Travel to Veeva offices may be required as needed.

Qualifications

• Experience understanding regulatory processes and requirements across life sciences functions.
• Strong research, analysis, and interpretation skills to identify relevant source information.
• Excellent written and verbal communication with ability to translate complex requirements for diverse teams.
• Highly organized with attention to detail and ability to work independently or in a team.
• Proficient with office software and ability to manage multiple priorities.

Responsibilities

• 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

Skills

Regulatory knowledge

Research & analysis

Communication skills

Detail-oriented

Self-starter

Teamwork

Time management

Tools

MS Office

Google Suite

Job description

Regulatory Intelligence Analyst job at Veeva Systems. Radnor, PA.

Veeva Systems is a mission‑driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest‑growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.

At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.

As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.

Join us in transforming the life sciences industry , committed to making a positive impact on its customers, employees, and communities.

The Role

We are looking for a Regulatory Intelligence Analyst to work alongside other analysts to ensure the product stays current with regulatory guidance, specifications, data standards, and requirements of global health authorities. You will identify, monitor, interpret, and communicate new or changing requirements to ensure the product stays current, and other internal teams are informed and knowledgeable of the latest regulatory intelligence. You will work directly with Product Management on compliance‑related features and with other Regulatory Intelligence Analysts to continually improve our internal processes.

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
• Flexible PTO and company paid holidays
• Retirement programs
• 1% charitable giving program

Compensation

• Base pay: $75,000 - $115,000
• 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.

Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.

Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at [e-mail].