RIM Implementation Consultant (Remote)

Veeva Consumer Products; Boston (MA); Remote; USD 65,000 - 145,000; Full time

Job summary

An established industry player is seeking a RIM Implementation Consultant to join their remote team. In this role, you will leverage your consulting experience to help life sciences customers optimize their regulatory data and document management processes. You will guide clients in configuring and implementing a unified software solution that streamlines global regulatory processes. This is an exciting opportunity to work in a dynamic environment where your contributions will directly impact the industry. If you are passionate about making a difference and thrive in a collaborative setting, this role is for you.

Benefits

Medical, dental, vision, and life insurance

Flexible PTO and paid holidays

Retirement plans

Charitable giving program

Qualifications

• 3+ years of experience in life sciences or healthcare.
• Technical skills to design and implement RIM solutions.

Responsibilities

• Guide customers in configuring and implementing Veeva’s Regulatory suite.
• Manage programs and projects, leading cross-functional teams.

Skills

Consulting

Regulatory Affairs

Communication

Project Management

Technical Skills

Collaboration

Education

Bachelor's Degree in Life Sciences or IT

Job description

Join to apply for the RIM Implementation Consultant (Remote) role at Veeva Consumer Products

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 a public benefit corporation (PBC), legally bound to balance 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

Veeva Systems seeks individual leaders with consulting and system implementation experience, passionate about helping customers optimize regulatory data and document management processes.

Veeva’s RIM suite is the industry’s only unified software solution providing fully integrated regulatory information management (RIM) capabilities, including data and document management, submission publishing, and archival on a cloud-based platform.

As part of our Professional Services team, you will understand our customers’ global regulatory needs, translate requirements into solution design, and configure our cloud-based solution for enterprise-wide regulatory information management.

This remote role is based in the U.S., preferably in the Eastern or Central Time Zone. Candidates near an airport and able to meet travel requirements are welcome to apply.

What You'll Do

1. Guide life science customers in configuring and implementing Veeva’s Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) to streamline global regulatory processes.
2. Lead configuration requirements workshops, design, document, prototype, and deploy solutions.
3. Manage programs and projects, including resource planning and leading cross-functional teams.
4. Communicate effectively between project teams, customers, and internal stakeholders.

Requirements

• 3+ years of experience in life sciences or healthcare, as a consultant, business, or IT professional.
• Technical skills and willingness to design, configure, and implement RIM solutions.
• Excellent collaboration and communication skills with diverse stakeholders.
• Strong organizational skills and ability to act swiftly in complex environments.
• Willingness to travel as required.

Nice to Have

• Experience with consulting, system integrators, or software vendors.
• Knowledge of drug development, Regulatory Affairs, or Regulatory Operations.
• Experience with compliance and validation in life sciences.

Perks & Benefits

• Medical, dental, vision, and life insurance.
• Flexible PTO and paid holidays.
• Retirement plans.
• Charitable giving program.

Compensation

• Base salary: $65,000 - $145,000, depending on experience and location.
• Additional compensation may include bonuses or stock options.

Veeva’s headquarters is in the San Francisco Bay Area, with offices worldwide. We are an equal opportunity employer. For accommodations, contact [e-mail].

Additional Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Information Technology
• Industry: Software Development