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Analyst II, Regulatory Medical Writing, Allschwil
Client:
Johnson and Johnson
Location:
Allschwil, Basel-Country, Switzerland
Job Reference:
bf19ca942ecb
Job Views:
3
Posted:
13.04.2025
Expiry Date:
28.05.2025
Job Description:
At 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.
Job Function: Medical Affairs Group
Job Sub Function: Medical Writing
Job Category: Professional
Analyst II, Regulatory Medical Writing
About Innovative Medicine: 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.
This is a hybrid or remote role available in all locations within Europe and North America. We invite candidates from any location to apply. Remote work options may be considered on a case-by-case basis and if approved by the Company.
We are searching for the best talent for Analyst II, Regulatory Medical Writing. As Analyst II, Regulatory Medical Writing, you will support one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, and Specialty Ophthalmology). Within our Regulatory Medical Writing team, you will join a cohort of writers undergoing internal training to author diverse regulatory medical writing documents. The target start date is 1 September 2025.
Responsibilities:
1. Write and coordinate clinical documents such as protocols, clinical study reports, tables of studies, narratives, and investigator’s brochures with oversight.
2. Perform document QC, literature searches, and other tasks.
3. Work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.
4. Partner with experienced colleagues on document planning, timelines, and content development according to internal processes.
5. Participate in or lead cross-functional document planning and review meetings independently or with oversight.
6. May participate in initiatives to improve medical writing processes and standards.
7. Acquire, maintain, and apply knowledge of industry, company, and regulatory guidelines.
8. Regularly meet with manager and mentors and attend departmental meetings.
Qualifications/Requirements:
1. A university/college degree in a scientific discipline is the minimum requirement, with an advanced degree (e.g., Master’s degree, PhD, MD) preferred.
2. At least 2 years of relevant pharmaceutical/scientific experience is required.
3. Strong oral and written communication skills in English.
4. Ability to understand, interpret, and summarize scientific or medical data.
5. Ability to function in a team environment and to build solid and positive relationships with cross‐functional team members.
6. Demonstrated problem-solving skills.
7. Strong attention to detail.
8. Strong time management and project/process management skills.
9. Demonstrated learning agility.
10. Sound knowledge of Microsoft Office programs (e.g., 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, and 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.
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