Enable job alerts via email!

Regulatory Systems Consultant

Pop Science

London

On-site

GBP 150,000 - 200,000

Full time

30+ days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An innovative firm is looking for a freelance Regulatory Systems Project Manager/Consultant to lead regulatory systems projects. This role involves overseeing the implementation and optimization of key regulatory systems, particularly the Veeva Vault RIM Suite. You will work closely with clients to devise strategies, enhance RIM capabilities, and ensure seamless integration with other business applications. The ideal candidate will have a strong background in regulatory operations within the pharmaceutical industry and excellent project management skills. Join a dynamic team where your expertise will drive significant improvements in regulatory systems processes.

Qualifications

  • Extensive experience in regulatory operations within the pharmaceutical industry.
  • Proficiency in managing RIM capabilities and driving process improvements.

Responsibilities

  • Oversee implementation and optimization of regulatory systems projects.
  • Collaborate with clients to enhance RIM capabilities and processes.

Skills

Analytical Skills
Problem-Solving
Decision-Making
Client Communication
Project Management

Education

Degree in Life Sciences
Degree in Information Technology
Degree in Regulatory Affairs

Tools

Veeva Vault RIM Suite
eCTD Management Systems
Electronic Document Management Systems (EDMS)

Job description

We are seeking a freelance Regulatory Systems Project Manager/Consultant to join our team. The successful candidate will be responsible for regulatory systems projects for our clients.

The project manager should be capable of overseeing the implementation, maintenance, and optimization of Veeva Vault RIM Suite. They should be able to work with clients to put together appropriate regulatory systems strategies and roadmaps and estimate resource requirements.

They should also be able to identify opportunities to enhance RIM capabilities and improve regulatory systems processes with the client, ensuring efficient data flow and communication between platforms. They will need to collaborate with cross-functional client teams to integrate RIM systems with other business applications and manage the integration of applicable regulatory systems and electronic document management systems (EDMS).

Experience required:
  1. Degree in Life Sciences, Information Technology, Regulatory Affairs, or related field
  2. Extensive experience in regulatory operations within the pharmaceutical industry
  3. Proficiency in Veeva Vault RIM Suite, eCTD management systems, and other regulatory systems
  4. Strong analytical, problem-solving, and decision-making abilities
  5. Understanding of Electronic Document Management Systems (EDMS)
  6. Experience in managing RIM capabilities and driving process improvements
  7. Experience in managing regulatory data and integration
  8. Excellent project management skills
  9. Ability to work in a client-facing environment with excellent written and verbal communication
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.