Director of Regulatory Writing

JR United Kingdom; Cheltenham; On-site; GBP 65,000 - 100,000; Full time

Job summary

A leading company in medical communications seeks a Director of Regulatory Writing to lead submissions and mentor team members. The role focuses on providing strategic regulatory writing support to clients in the pharmaceutical industry. This position offers a chance to work with a reputable team while receiving flexible time off and professional development opportunities.

Benefits

Flexible Time Off – uncapped paid time off

Retail and gym discounts

Training and development opportunities

Employee assistance programme

Private healthcare

Headspace and MYNDUP mental health programmes

Cycle to work scheme

Season Ticket Loan

Flexible working arrangements

Qualifications

• Experience in regulatory or medical writing within the pharmaceutical industry.
• Ability to lead complex submissions.
• Strong client relationship management skills.

Responsibilities

• Lead complex submissions and guide team members.
• Maintain excellent client relationships and provide high-level leadership.
• Consult with clients across different project types and therapy areas.

Skills

Regulatory Writing

Medical Writing

Strategic Thinking

Job description

Who are we?

Complete Regulatory is part of IPG Health Medical Communications, home to the world’s most celebrated and awarded Med Comms agencies. We are 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, producing a wide range of high-quality clinical documentation, including clinical study reports, protocols, summaries, overviews, regulatory responses, and other supporting documents across various therapy areas.

The role

We are seeking experienced Directors of Regulatory Writing with prior experience in regulatory or medical writing within the pharmaceutical industry or agencies to join our team. You will lead complex submissions and guide other team members, utilizing your thorough knowledge of regulatory documents and submission development.

Our clients highly value our services. In this role, you will work as a trusted partner with various companies, providing high-level leadership and support across different project types and therapy areas. You will maintain excellent client relationships, 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 regulatory writing experience within a supportive and reputable team. You will also be part of a larger organization offering world-class services and flexible organizational structures.

Benefits include:

• Flexible Time Off – uncapped paid time off
• Retail and gym discounts
• Training and development opportunities
• Employee assistance programme
• Private healthcare
• Headspace and MYNDUP mental health programmes
• 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 celebrates diversity and encourages applicants from all backgrounds and abilities. We aim to provide equal opportunities and reasonable adjustments during our assessment process. Please let us know if any accommodations are needed.