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- Tasks: Join our team to write and coordinate essential clinical documents in a dynamic environment.
- Company: Be part of Johnson & Johnson, a leader in healthcare innovation dedicated to improving lives.
- Benefits: Enjoy a competitive salary, flexible working options, and career development opportunities.
- Why this job: Make a real impact on health while collaborating with passionate professionals in a supportive culture.
- Qualifications: A degree in a scientific field is required; advanced degrees and relevant experience are preferred.
- Other info: This role offers hybrid work options and is available across multiple countries.
The predicted salary is between 28800 - 48000 £ per year.
Analyst II, Regulatory Medical Writing X-TA
Join to apply for the Analyst II, Regulatory Medical Writing X-TA role at Johnson & Johnson Innovative Medicine
Analyst II, Regulatory Medical Writing X-TA
Join to apply for the Analyst II, Regulatory Medical Writing X-TA role at Johnson & Johnson Innovative Medicine
Get AI-powered advice on this job and more exclusive features.
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at https://www.jnj.com
Job Function
Medical Affairs Group
Job Sub Function
Medical Writing
Job Category
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description
Analyst II, Regulatory Medical Writing X-TA
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 are searching for the best talent for Analyst II, Regulatory Medical Writing, X-TA located UK, EU or Canada (Hybrid) (2 available positions).
As Analyst II, Regulatory Medical Writing X-TA, you will support across one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, Specialty Ophthalmology) within our Regulatory Medical Writing team, to author diverse regulatory medical writing documents. Hybrid (3 days onsite per week) is preferred. Remote work options may be considered on a case-by-case basis and if approved by the Company.
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):
United Kingdom – Requisition Number: R-021736
EU (Belgium, France, Germany, Netherlands) – Requisition Number: R-023564
Canada – Requisition Number: R-023566
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Purpose
- 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 / Requirements
- 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 is required.
- Strong oral and written communication skills in English.
- Ability to understand, interpret, and summarize scientific or medical data.
- Ability to function in a team environment and to build solid and positive relationships with cross‐functional team members.
- Demonstrated problem-solving skills.
- Strong attention to detail.
- Strong time management and project/process management skills.
- Demonstrated learning agility.
- Sound knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook).
Benefits
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
All qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform important job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodations.
Seniority level
-
Seniority level
Not Applicable
Employment type
-
Employment type
Full-time
Job function
-
Job function
Finance and Sales
-
Industries
Pharmaceutical Manufacturing
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Analyst II, Regulatory Medical Writing X-TA employer: Johnson & Johnson Innovative Medicine
Contact Detail:
Johnson & Johnson Innovative Medicine Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Analyst II, Regulatory Medical Writing X-TA
✨Tip Number 1
Familiarise yourself with the specific therapeutic areas mentioned in the job description, such as Oncology and Immunology. This knowledge will not only help you understand the role better but also allow you to engage in meaningful conversations during interviews.
✨Tip Number 2
Network with professionals already working in regulatory medical writing or related fields. Use platforms like LinkedIn to connect with current employees at Johnson & Johnson, as they can provide valuable insights and potentially refer you for the position.
✨Tip Number 3
Brush up on your knowledge of regulatory guidelines and standards relevant to medical writing. Being well-versed in these areas will demonstrate your commitment and readiness for the role, making you a more attractive candidate.
✨Tip Number 4
Prepare to discuss your experience with document coordination and quality control during the interview. Highlight specific examples where you've successfully managed timelines and collaborated with cross-functional teams, as these skills are crucial for the Analyst II role.
We think you need these skills to ace Analyst II, Regulatory Medical Writing X-TA
Some tips for your application 🫡
Understand the Role: Before applying, make sure you thoroughly understand the responsibilities and qualifications for the Analyst II, Regulatory Medical Writing X-TA position. Tailor your application to highlight relevant experiences that align with the job description.
Craft a Strong CV: Your CV should clearly outline your educational background, relevant work experience, and skills that match the requirements of the role. Emphasise your scientific discipline degree and any specific medical writing experience you have.
Write a Compelling Cover Letter: In your cover letter, express your passion for medical writing and how your skills can contribute to Johnson & Johnson's mission. Be sure to mention your understanding of regulatory guidelines and your ability to work in a team environment.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role in regulatory medical writing.
How to prepare for a job interview at Johnson & Johnson Innovative Medicine
✨Understand the Role
Before your interview, make sure you thoroughly understand the responsibilities of the Analyst II, Regulatory Medical Writing position. Familiarise yourself with the types of documents you'll be writing and the therapeutic areas involved, such as Oncology and Immunology.
✨Showcase Your Communication Skills
As this role requires strong oral and written communication skills, prepare to demonstrate these during the interview. Be ready to discuss how you've effectively communicated complex scientific data in previous roles.
✨Prepare for Teamwork Questions
Since the job involves working in a matrix environment, expect questions about teamwork and collaboration. Think of examples where you've successfully worked with cross-functional teams and how you built positive relationships.
✨Highlight Your Attention to Detail
Attention to detail is crucial in regulatory writing. Prepare to discuss specific instances where your attention to detail made a significant impact on a project or document. This will show your potential employer that you take quality seriously.
