Global MedTech RIM Implementation Lead

Veeva; Chicago (IL); On-site; USD 80,000 - 200,000; Full time

Benefits offered by this job

Medical, dental, vision, and life insurance

Flexible PTO and company paid holidays

Retirement programs

1% charitable giving program

Job summary

Veeva Systems, based in Chicago, is seeking an experienced consultant to lead MedTech Regulatory Information Management (RIM) implementations. This role involves guiding customers through Regulatory Affairs and Operations processes with industry-leading technology.

Applicants should have over 8 years of experience in Systems Implementation and strong knowledge of global regulatory requirements. The position offers a hybrid work environment and a range of benefits including flexible PTO and retirement programs.

Qualifications

• 8+ years of experience in Systems Implementation, GxP Systems ownership, or Software Consulting.
• 4+ years of experience in Regulatory Operations or Regulatory Affairs within the Medical Device or Diagnostics industry.
• Direct experience with software implementation for Veeva RIM or similar solutions.

Responsibilities

• Lead RIM implementation workstreams for MedTech Regulatory solutions.
• Review and analyze existing customer business processes.
• Function as a primary customer liaison managing complex communication.

Skills

Systems Implementation

Regulatory Operations

Consulting

Change Management

Communication

Tools

Veeva RIM

RegDesk

RIMSYS

IQVIA

Kalypso

Essenvia

Job description

Veeva Systems, based in Chicago, is seeking an experienced consultant to lead MedTech Regulatory Information Management (RIM) implementations. This role involves guiding customers through Regulatory Affairs and Operations processes with industry-leading technology.

Applicants should have over 8 years of experience in Systems Implementation and strong knowledge of global regulatory requirements. The position offers a hybrid work environment and a range of benefits including flexible PTO and retirement programs.