Minimum 3 years of experience in life sciences or healthcare industries, either as a consultant or in a related role., Technical skills in designing, configuring, and implementing Regulatory Information Management (RIM) solutions., Strong communication and collaboration skills to work with diverse stakeholders., Ability to travel as required and work remotely, with a preference for candidates in the Eastern or Central Time Zone..
Key responsibilities:
Guide clients in configuring and implementing Veeva's Regulatory suite to optimize regulatory processes.
Lead requirements workshops, design solutions, and oversee deployment of the software.
Manage projects and resources, ensuring effective communication among team members and clients.
Collaborate with cross-functional teams to ensure successful system implementation.
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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 missiondriven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastestgrowing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.