Analyst II, Regulatory Medical Writing Immunology

Johnson & Johnson; England; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading global healthcare company is seeking an Analyst II in Regulatory Medical Writing to support the Immunology team. Responsibilities include authoring clinical documents, performing quality checks, and ensuring compliance with regulatory standards. The position offers hybrid work options from the UK, with a focus on career development and a balanced work-life environment. Join a team dedicated to transforming patient insights into advancements in medicine.

Benefits

Competitive salary

Extensive benefits package

Career development opportunities

Flexible working environment

Work-life balance

Qualifications

• At least 2 years of relevant pharmaceutical/scientific experience.
• 1 year of regulatory medical writing experience preferred.
• Ability to summarize and present statistical and medical information.

Responsibilities

• Write and coordinate clinical documents with oversight.
• Perform document QC, literature searches, and other tasks.
• Participate in cross-functional document planning and review meetings.

Skills

Attention to detail

Strong oral and written communication skills

Problem Solving

Medical Writing

Data Gathering Analysis

Clinical Research and Regulations

Education

University/college degree in a scientific discipline

Advanced degree (Master's, PhD, MD)

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Outlook

Job description

Purpose

We are searching for the best talent for Analyst II, Regulatory Medical Writing, Immunology within our Integrated Data Analytics & Reporting (IDAR) business. The position may be located High Wycombe, UK; Leiden, Netherlands or Beerse, Belgium. The position is hybrid (3 days onsite weekly). Remote work options may be considered on a case‑by‑case basis and if approved by the company. As Analyst II, Regulatory Medical Writing, you will support across the Immunology therapeutic area within our Regulatory Medical Writing team, to author diverse regulatory medical writing documents. Are you ready to join our team? Then please read further!

• Develop within the medical writing role within the pharmaceutical industry.
• Work in a team environment and matrix.
• Gain knowledge and apply internal standards, regulatory, and publishing guidelines.
• Learn and use internal systems, tools, and processes.
• Write and coordinate basic documents and help to prepare more complex documents.
• Perform routine tasks per established procedures.

You Will Be Responsible For

• Write and coordinate clinical documents such as protocols, clinical study reports, tables of studies, narratives, and investigator's brochures with oversight.
• Perform document QC, literature searches, and other tasks.
• Work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.
• Partner with experienced colleagues on document planning, timelines, and content development according to internal processes.
• Participate in or lead cross‑functional document planning and review meetings independently or with oversight.
• May participate in initiatives to improve medical writing processes and standards.
• Acquire, maintain, and apply knowledge of industry, company, and regulatory guidelines.
• Regularly meet with manager and mentors and attend departmental meetings.

Qualifications

• A university/college degree in a scientific discipline is the minimum requirement, with an advanced degree (eg, Master's degree, PhD, MD) preferred.
• At least 2 years of relevant pharmaceutical/scientific experience; at least 1 year of regulatory medical writing experience is preferred.
• Ability to learn and recognize how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content in document types under supervision.
• Attention to detail.
• Strong oral and written communication skills.
• Emerging leadership skills, both in time management as well as in project/process management.
• Able to resolve basic problems independently and complex problems under supervision.
• Demonstrate learning agility.
• Able to build solid and positive relationships with cross‑functional team members.
• Sound knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook).

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s).

Preferred Skills

• Medical Writing
• Regulatory Writing
• Business Behavior
• Business Writing
• Clinical Research and Regulations
• Clinical Trials Operations
• Coaching
• Collaborating
• Copy Editing
• Data Gathering Analysis
• Data Savvy
• Document Management
• Industry Analysis
• Medical Affairs
• Medical Communications
• Problem Solving
• Process Oriented
• Proofreading
• Quality Standards
• Research Ethics

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science‑based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine

We offer a competitive salary and extensive benefits package. The health and well‑being of our employees is a priority, we have a flexible working environment as we value work‑life balance. We offer career development opportunities for those who want to grow and be part of our organisation. For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefits