MedTech Regulatory RIM Lead — Remote

Veeva Systems; Minneapolis (MN); On-site; USD 80,000 - 200,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

Flexible PTO

Retirement programs

Charitable giving program

Job summary

Veeva Systems, a pioneer in industry cloud, is seeking an experienced consultant to lead MedTech Regulatory Information Management implementations. The role involves guiding regulatory processes and ensuring successful adoption of Veeva’s solutions. Ideal candidates should have over 8 years of systems implementation experience, particularly within medical devices. The position offers the flexibility to work remotely, a strong emphasis on customer and employee success, and substantial compensation ranging from $80,000 to $200,000 depending on experience.

Qualifications

• 8+ years of experience in Systems Implementation or Software Consulting.
• 4+ years working in Regulatory Affairs in Medical Devices.
• Strong understanding of global regulatory requirements.

Responsibilities

• Lead RIM implementation workstreams for customer solutions.
• Review customer business processes to identify key requirements.
• Function as a primary customer liaison for implementation teams.

Skills

Systems Implementation

Regulatory Operations

Communication Skills

Tools

Veeva RIM

RegDesk

IQVIA

Job description

Veeva Systems, a pioneer in industry cloud, is seeking an experienced consultant to lead MedTech Regulatory Information Management implementations. The role involves guiding regulatory processes and ensuring successful adoption of Veeva’s solutions. Ideal candidates should have over 8 years of systems implementation experience, particularly within medical devices. The position offers the flexibility to work remotely, a strong emphasis on customer and employee success, and substantial compensation ranging from $80,000 to $200,000 depending on experience.