Johnson & Johnson

Science and healthcare-focused role with an interest in medical writing and regulatory documentation, working in a hybrid environment combining detailed writing, data interpretation, and cross-functional collaboration.DescriptionAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job Description:About Innovative MedicineOur 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.We are searching for the best talent for Medical Writer I to support one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, and Cardiopulmonary) within the Regulatory Medical Writing unit.As a Medical Writer I, within Regulatory Medical Writing, you will join a cohort of medical writers undertaking internal training to author a range of regulatory medical writing documents. The cohort’s target start date is 1 September 2026, and candidates must be available to commence the role at this time.This is a hybrid position requiring three days per week on site. The role can be based in High Wycombe/ UK (moving to Maidenhead in October 2026), Beerse/ Belgium, or Leiden/ Netherlands. Candidates must be located within commutable distance of one of these offices or be willing to self‑relocate within the same country.Remember, whether you apply to one or both of these requisition numbers, your applications will be considered as a single submission.Purpose:Learn the regulatory medical writing role and pharmaceutical industry and business.Learn to work in a team environment and matrix.Learn internal standards, regulatory, and publishing guidelines.Learn internal systems, tools, and processes.Help to prepare sections of documents and prepare basic documents under supervision.Assist with routine tasks per established procedures.You will be responsible for:Prepare components of clinical and regulatory documents and write basic documents such as tables of studies, narratives, protocol amendments, investigator’s brochure updates and addenda under supervision.May assist with document QC, abbreviations, references, literature searches, and other tasks.Learn how to interpret, summarize, and present statistical and medical information.Learn to work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.Attend cross-functional meetings with other writers as appropriate (eg, project kick-off and review meetings).Learn and adhere to SOPs, templates, best practices, policies, and Medical Writing Style Guide.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.Strong oral and written communication skills in English.Ability to understand and summarize scientific data.Ability to function in a team environment and to build solid and positive relationships with co-workers.Demonstrated problem-solving skills.Attention to detail.Organizational skills and time management skills.Demonstrated learning agility.Ability to learn and apply knowledge of regulatory guidance documents such as ICH requirements.Working knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook).BenefitsWe 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. 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.

Posted 13 days ago

Science and clinical research-focused role with an interest in healthcare and medical innovation, working in a structured, office-based or hybrid environment supporting research coordination and compliance activities.DescriptionAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.DePuy Synthes offer the world’s largest portfolio of orthopaedic products and services designed to advance patient care and deliver clinical and economic value globally. Inspired by the opportunity to help people return to living active and fulfilling lives, we bring surgeons and healthcare providers together to create value by increasing patient satisfaction, improving clinical outcomes and reducing costs.This role in our Clinical Research department will be responsible for providing administrative assistance to the External Research Leaders in the management of the external research portfolio, with a focus on Scientific Investigator Initiated Studies (IIS), ensuring compliance with company policies and legal requirements.OVERALL RESPONSIBILITIES: Responsible for coordination of Scientific Investigator-initiated study (IIS) and Collaborative study (CS) activities. Including, but not limited to: Scheduling Scientific IIS committee meetings and coordinating committee members Meeting agenda preparation Monthly decision log creation and distribution Assisting with proposal review Communications with study managers Ensuring complete study documentation Oversight of study updates and finances Keeps abreast of clinical research methodologies to understand and translate advances in clinical science into the franchise clinical research strategies and protocols. Keeps abreast of regulatory requirements and industry standards on scientific communication and publication development. Performs work under supervision, and seeks guidance where required. No direct reports, but may mentor clinical support staff, summer hires, and clinical interns.• Follow all laws and policies that apply to the role, and maintain the highest levels of professionalism, ethics and compliance at all times.• Diligently participate in our compliance related activities as denoted by the company.• May be involved in other tasks to support External Research activities, as needed.EDUCATION & EXPERIENCE REQUIREMENTS:A bachelors or equivalent degree in Life Sciences or related discipline, or equivalent relevant working experience, is required.Prior experience of clinical research is preferable.Experience with medical devices is desirable.ADDITIONAL SKILLS:Demonstrated competencies in the following areas are required:Leadership in a professional and ethical manner.Presentation skills and influencing of others.Written and oral communication skills.Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Posted 13 days ago