Regulatory Training Lead – Veeva RIM Specialist

SRG; Greater London; Hybrid; GBP 125,000 - 150,000; Full time

Job summary

A global pharmaceutical company is seeking a Regulatory Affairs Training Manager for an 18-month hybrid position in London. This role involves developing training materials, coordinating training sessions for Super Users and End Users, and managing training resources post implementation of Veeva RIM. Candidates should have a Life Science Degree and strong project management skills. This position offers a competitive rate of £430 per day via an umbrella company.

Qualifications

• Life Science Degree or other University degree with equivalent experience required.
• Strong training delivery capability needed.
• Good understanding of all RA roles is essential.

Responsibilities

• Develop and publish program training materials related to Veeva RIM.
• Coordinate delivery of training sessions for Super Users and End Users.
• Maintain and update training materials post Go-live.

Skills

Strong training and communications skills

Project management skills

Experience with Veeva RIM deployments

Technology-savvy

Strong communication skills

Education

Life Science Degree or equivalent

Tools

Project management tools

Job description

A global pharmaceutical company is seeking a Regulatory Affairs Training Manager for an 18-month hybrid position in London. This role involves developing training materials, coordinating training sessions for Super Users and End Users, and managing training resources post implementation of Veeva RIM. Candidates should have a Life Science Degree and strong project management skills. This position offers a competitive rate of £430 per day via an umbrella company.