Director of Regulatory Writing

JR United Kingdom; Oxford; On-site; GBP 60,000 - 90,000; Full time

Job summary

A leading company in medical communications seeks a Director of Regulatory Writing to lead submissions for regulatory authorities. This role emphasizes client engagement and requires in-depth knowledge of regulatory documents to support diverse projects. Join a supportive team and benefit from flexible working arrangements and comprehensive training.

Benefits

Flexible Time Off – uncapped paid time off

Retail and gym discounts

Comprehensive training and development

Employee assistance program

Private healthcare

Headspace and MYNDUP mental health programs

Cycle to work scheme

Season Ticket Loan

Flexible working arrangements

Qualifications

• Experience as a regulatory writer within the pharmaceutical industry or medical writing agencies.
• Lead submissions and support team members.
• Strong client consulting and strategic planning skills.

Responsibilities

• Guide team members in regulatory submissions.
• Maintain excellent client relationships and provide leadership.
• Consult with clients on medical writing needs for regulatory authorities.

Skills

Regulatory document knowledge

Client relationship management

Leadership

Strategic thinking

Job description

Who are we?

Complete Regulatory is part of IPG Health Medical Communications, which is home to some of the world’s most celebrated and awarded Med Comms agencies. We are a team of 800 experts dedicated to combining science, creativity, and technology to create exceptional medical communications solutions for our clients.

What do we do?

At Complete Regulatory, we provide leading writing support and consultancy services to the pharmaceutical industry. We produce a wide range of high-quality clinical documentation, including clinical study reports, protocols, clinical summaries, clinical overviews, regulatory responses, and other supporting documents across various therapy areas.

The role

We are seeking experienced Directors of Regulatory Writing with prior experience as regulatory writers within the pharmaceutical industry or medical writing agencies. In this role, you will lead complex submissions and guide team members, utilizing your thorough knowledge of regulatory documents and submission development.

You will work as a trusted partner with clients, providing high-level leadership and support across diverse project types and therapy areas. Maintaining excellent client relationships, you will consult with clients and demonstrate strategic thinking to ensure effective medical writing for regulatory authorities.

What will you get in return?

This position offers an excellent opportunity to build on your regulatory writing experience within a highly specialized, supportive, and reputable team. You will also become part of a larger organization offering world-class services and a flexible structure.

Benefits include:

• Flexible Time Off – uncapped paid time off
• Retail and gym discounts
• Comprehensive training and development
• Employee assistance program
• Private healthcare
• Headspace and MYNDUP mental health programs
• Cycle to work scheme
• Season Ticket Loan
• Flexible working arrangements

To Apply or Contact Us

Apply by clicking the link below.

IPG Health Medical Communications is committed to diversity and encourages applicants from all backgrounds and abilities. Please let us know if any reasonable adjustments are needed during the application process.