3+ years of experience in commercial software, quality assurance, clinical development, or regulatory affairs in the life sciences industry., Working knowledge of regulatory processes in at least one regulated sector of the life sciences industry., Excellent research, analysis, and communication skills, with the ability to simplify complex regulatory information., Highly organized, detail-oriented, and proficient in office software like MS Office and Google Suite..
Key responsabilities:
Identify and monitor regulatory requirements related to the product and communicate changes to internal teams.
Proactively investigate and interpret changes to regulatory requirements that may impact the product.
Collaborate with product management to translate regulatory requirements into Veeva’s application framework.
Work with a team to improve processes for collecting and managing regulatory intelligence.
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Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 875 customers, ranging from the world's largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices in Canada, Europe, Asia, and Latin America. Veeva is growing to 10,000 employees by 2025, so visit the Jobs section for open positions and remember that correspondence to new applicants and existing candidates will only come from an official @veeva.com email address.
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.
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.
#LI-Remote
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 talent_accommodations@veeva.com.
Required profile
Experience
Industry :
Computer Software / SaaS
Spoken language(s):
English
Check out the description to know which languages are mandatory.