Director of Regulatory Writing

JR United Kingdom; Hemel Hempstead; On-site; GBP 60,000 - 80,000; Full time

Job summary

JR United Kingdom is seeking experienced Directors of Regulatory Writing to join their team at Complete Regulatory. This key role involves leading regulatory submissions, managing client relationships, and leveraging deep industry knowledge for effective medical documentation. Successful candidates will enjoy flexible working arrangements and extensive professional development opportunities.

Benefits

Flexible Time Off – uncapped paid time off

Retail and gym discounts

Comprehensive training and development

Employee assistance programme

Private healthcare

Mental health programmes

Cycle to work scheme

Season Ticket Loan

Flexible working options

Qualifications

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

Responsibilities

• Lead complex regulatory submissions and guide team members.
• Maintain strong client relationships and consult on projects.
• Apply expertise in regulatory documents for submissions.

Skills

Regulatory writing

Client relationship management

Leadership

Job description

Who are we?

Complete Regulatory is part of IPG Health Medical Communications, 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 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 in regulatory or medical writing within the pharmaceutical industry or a medical communications agency. In this role, you will lead complex submissions, guide team members, and leverage your extensive knowledge of regulatory documents and submission development.

You will work closely with clients as a trusted partner, providing strategic leadership on diverse projects and therapy areas. Maintaining strong client relationships, you will consult with clients and apply your expertise to ensure effective medical writing for regulatory authorities.

What will you get in return?

This role offers an excellent opportunity for those looking to enhance their regulatory writing experience within a supportive and reputable team. You will also benefit from being part of a larger organization offering world-class services and flexible working arrangements.

Additional benefits include:

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

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. If you require any reasonable adjustments during the application process, please let us know to ensure a fair assessment.