Medical Writer (Regulatory) in Hull
Medical Writer (Regulatory)

Medical Writer (Regulatory) in Hull

Hull Full-Time 36000 - 60000 £ / year (est.) Home office possible
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Bioscript Group

At a Glance

  • Tasks: Lead and develop high-quality regulatory documents while mentoring junior team members.
  • Company: Bioscript Group, a supportive and innovative company in the pharmaceutical sector.
  • Benefits: Competitive salary, generous holiday, enhanced leave, and private medical insurance.
  • Why this job: Make a real impact in the pharmaceutical industry while growing your career.
  • Qualifications: Strong technical skills in regulatory writing and excellent communication abilities.
  • Other info: Join a diverse team focused on exceptional delivery and personal development.

The predicted salary is between 36000 - 60000 £ per year.

Business Unit: Bioscript Regulatory Writing

Location: UK or Europe (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.

We are committed to creating an inclusive and diverse workplace. We encourage applications from all individuals who meet the minimum requirements of the role. If you require any reasonable adjustments during the application or interview process, please contact us via or by calling 01625 908246.

Medical Writer (Regulatory) in Hull employer: Bioscript Group

Bioscript Group is an exceptional employer that prioritises the well-being and development of its employees, offering a supportive and inclusive work culture. With opportunities for career growth, comprehensive benefits including generous holiday allowances, enhanced leave policies, and a commitment to community engagement, Bioscript Group empowers its team members to thrive both professionally and personally while working remotely from the UK or Europe.
Bioscript Group

Contact Detail:

Bioscript Group Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Medical Writer (Regulatory) in Hull

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory writing field on LinkedIn or at industry events. A friendly chat can open doors that a CV just can't.

✨Tip Number 2

Prepare for interviews by researching the company and its projects. Show us you’re genuinely interested in Bioscript Group and how your skills can contribute to our mission.

✨Tip Number 3

Practice your communication skills! As a Medical Writer, you'll need to convey complex information clearly. Mock interviews with friends can help you nail this.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take that extra step.

We think you need these skills to ace Medical Writer (Regulatory) in Hull

Regulatory Writing
Technical Writing
Scientific Leadership
Project Management
Coaching and Mentoring
Communication Skills
Document Quality Assurance
Knowledge Transfer
Budget Management
Client Relationship Management
Attention to Detail
Ability to Manage Multiple Projects
Proactive Knowledge Sharing
Team Development

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the role of a Medical Writer. Highlight your experience in regulatory writing and any relevant projects you've worked on. We want to see how your skills align with what we're looking for!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about regulatory writing and how you can contribute to our team. Keep it concise but impactful – we love a good story!

Showcase Your Communication Skills: As a Medical Writer, clear communication is key. In your application, demonstrate your ability to convey complex information simply and effectively. We’re looking for clarity and precision in your writing!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you’ll find all the details you need about the role there!

How to prepare for a job interview at Bioscript Group

✨Know Your Regulatory Stuff

Make sure you brush up on the latest regulatory guidelines and standards relevant to the pharmaceutical industry. Being able to discuss these confidently will show that you're not just familiar with the basics, but that you’re also committed to staying updated in this ever-evolving field.

✨Showcase Your Writing Skills

Prepare a portfolio of your previous regulatory documents or writing samples. During the interview, be ready to discuss your writing process, how you ensure clarity and accuracy, and any challenges you've faced in past projects. This will demonstrate your expertise and attention to detail.

✨Be a Team Player

Since the role involves coaching and mentoring junior team members, think of examples where you've successfully led a team or supported colleagues. Highlight your communication skills and how you foster collaboration, as this is key to thriving in their supportive environment.

✨Ask Insightful Questions

Prepare thoughtful questions about the company’s approach to regulatory writing and team dynamics. This shows your genuine interest in the role and helps you gauge if the company culture aligns with your values. Plus, it gives you a chance to engage with the interviewers on a deeper level.

Medical Writer (Regulatory) in Hull
Bioscript Group
Location: Hull
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