Senior Medical Writer (Regulatory)

JR United Kingdom; Hounslow; Hybrid; GBP 45,000 - 65,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Senior Medical Writer to join their hybrid UK team. The role involves leading a regulatory writing team, ensuring high-quality documentation, and managing various client projects. Candidates must possess strong technical skills and excellent communication abilities, as well as the capability to mentor junior staff. The company values career development and offers a comprehensive benefits package including generous holiday allowances and enhanced leave policies.

Benefits

25 days holiday + bank holidays

Enhanced sick leave

Bonus day off for community service

Private Medical Insurance

Qualifications

• Strong technical and scientific skills with experience in developing high-quality regulatory documents.
• Excellent communication skills and the ability to coach and mentor junior team members.
• Ability to manage multiple projects and deliver high-quality work within deadlines.

Responsibilities

• Lead regulatory writing team and manage project deliverables.
• Take responsibility for the delivery of multiple projects ensuring quality that meets brief.
• Support development of regulatory writing training program.

Skills

Technical skills

Scientific writing

Communication skills

Project management

Job description

Social network you want to login/join with:

Senior Medical Writer (Regulatory), south west london

col-narrow-left

Client:

Location:

south west london, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

10

Posted:

06.06.2025

Expiry Date:

21.07.2025

col-wide

Job Description:

Role: Senior / Principal Regulatory Writer

Business Unit: Bioscript Regulatory Writing

Location: UK (Hybrid or UK remote)

About Us

Established in 2005, Bioscript Group is formed from multiple, specialist businesses to support our global pharmaceutical clients; we provide multidisciplinary expertise to help our clients navigate critical decisions at key points in the product lifecycle.

Our scientific and strategic expertise help our clients make better decisions. We provide medical communication services, market access consulting and regulatory writing support with deep domain expertise to effectively navigate complex disease areas.

The Opportunity

We are hiring for both Senior Regulatory Writer (SRW) and Principal Regulatory Writer (PRW) positions. This is a fantastic opportunity to join our friendly and supportive team and lead the development of high-quality regulatory documents. You will work closely with our clients and internal teams, providing technical and scientific leadership, and ensuring the delivery of clear, accurate, well-written documents.

Key Responsibilities (SRW and PRW)

• Lead and motivate regulatory writing team members, adhering to company policies and procedures. Coach and mentor more junior team members, providing support and guidance on client and project-related issues
• Be the point of contact for specific project deliverables, managing the technical and scientific aspects of leadership of designated client accounts/teams
• Take responsibility for the delivery of multiple projects across client accounts, ensuring high-quality work that meets the project/client brief, timelines, and budget
• Track and manage project scope in collaboration with the Project Management team, demonstrating a sound understanding of budgets
• Proactively share knowledge and experience to support the transfer of knowledge across the team
• Support development of the regulatory writing training programme, as appropriate
• Line management, if consistent with company needs and personal aspirations

Additional PRW Responsibilities

• Lead strategic and high-complexity programs such as submissions
• Be a key source of account, product, or therapy area expertise to clients and colleagues
• Advise on regulatory writing processes and strategy, document quality process, client procedures, and best practice for projects
• Contribute to group discussions, sharing opinions and professional values
• Support the Project Management team with development or review of budgets against project specifications, if required
• Contribute to ongoing recruitment programmes, assisting with candidate assessment and the interview process, if required

About You

• Strong technical and scientific skills with experience in developing high-quality regulatory documents
• Excellent communication skills and the ability to coach and mentor junior team members, providing support and guidance on client and project-related issues
• Ability to manage multiple projects and deliver high-quality work within deadlines, ensuring the production of clear, accurate, and grammatically correct written work
• A proactive approach to sharing knowledge and supporting team development, contributing to the transfer of knowledge across the team

Our people are at the heart of our business

We are focused on delivering the exceptional, not just for our clients, but for our teams too. We treat everyone as individuals and provide opportunities to develop your skills and career around our disciplines.

Our benefits include:

• Salary which aligns with your experience and skillset
• 25 days holiday + bank holidays + winter shutdown + holiday purchase scheme
• Enhanced sick and compassionate leave
• Enhanced maternity, paternity and adoption leave
• Birthday donation to a charity of your choice
• Bonus day off to be spent giving back to the community
• Life Insurance and Critical Illness cover
• Private Medical Insurance (Vitality for UK based colleagues)
• Health cash plan or wellbeing allowance
• International Employee Assistance Program