WayUp
Johnson & Johnson, Analyst II, Medical Writing, Immunology - Application via Way
WayUp, Titusville, New Jersey, us, 08560
Johnson & Johnson, Analyst II, Medical Writing, Immunology
2 days ago – Be among the first 25 applicants. This role is with Johnson & Johnson. WayUp is partnering with Johnson & Johnson to hire top talent.
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. Learn more at
https://www.jnj.com .
Job Details
Job Function: Medical Affairs Group
Job Sub Function: Medical Writing
Job Category: Professional
Locations: High Wycombe, Buckinghamshire, United Kingdom; Leiden, South Holland, Netherlands; Raritan, New Jersey, United States; Spring House, Pennsylvania, United States; and other locations worldwide. Remote work may be considered on a case‑by‑case basis.
Requisition Numbers:
United States – R‑032561
Belgium & Netherlands – R‑033141
United Kingdom – R‑033139
Switzerland – R‑033138
Purpose The Analyst II, Medical Writing, Immunology develops, writes, and coordinates clinical and regulatory documents across therapeutic areas, supporting drug development from early discovery through commercialization.
Responsibilities
Write and coordinate Phase 1‑3 clinical documents such as protocols, CSRs, study tables, narratives, and investigator brochures.
Prepare and review low‑ to medium‑complexity medical writing deliverables under supervision.
Conduct document quality control, literature searches, and abbreviation lists.
Participate in cross‑functional writing and planning meetings.
Establish document timelines and strategies, maintaining compliance with SOPs and internal standards.
Mentor junior writers and guide cross‑functional team members on best practices.
Track project milestones, report status, and update project management systems.
Qualifications
University or college degree in a scientific discipline; an advanced degree (Masters, PhD, MD) preferred.
Minimum 2 years of relevant pharmaceutical or scientific experience.
Experience writing medical documents (Phase 1‑3 CSRs, protocols, investigator brochures). 0‑4 years of regulatory writing experience is acceptable based on supervision level.
Strong oral and written communication skills with a high attention to detail.
Ability to work in a team environment, organize time effectively, and demonstrate learning agility.
Knowledge of ICH regulatory guidance and the Medical Writing Style Guide.
Emerging leadership skills in project, process, and time management.
Compensation & Benefits Salary range: $89,000 – $143,750 per year. Expectations include an annual performance bonus and participation in the company’s benefit programs (health, dental, vision, 401(k), paid time off, holiday pay, and other standard benefits). Detailed compensation is tailored by location.
EEO Statement Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, or protected veteran status. We actively seek qualified candidates who are protected veterans and individuals with disabilities.
#J-18808-Ljbffr
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. Learn more at
https://www.jnj.com .
Job Details
Job Function: Medical Affairs Group
Job Sub Function: Medical Writing
Job Category: Professional
Locations: High Wycombe, Buckinghamshire, United Kingdom; Leiden, South Holland, Netherlands; Raritan, New Jersey, United States; Spring House, Pennsylvania, United States; and other locations worldwide. Remote work may be considered on a case‑by‑case basis.
Requisition Numbers:
United States – R‑032561
Belgium & Netherlands – R‑033141
United Kingdom – R‑033139
Switzerland – R‑033138
Purpose The Analyst II, Medical Writing, Immunology develops, writes, and coordinates clinical and regulatory documents across therapeutic areas, supporting drug development from early discovery through commercialization.
Responsibilities
Write and coordinate Phase 1‑3 clinical documents such as protocols, CSRs, study tables, narratives, and investigator brochures.
Prepare and review low‑ to medium‑complexity medical writing deliverables under supervision.
Conduct document quality control, literature searches, and abbreviation lists.
Participate in cross‑functional writing and planning meetings.
Establish document timelines and strategies, maintaining compliance with SOPs and internal standards.
Mentor junior writers and guide cross‑functional team members on best practices.
Track project milestones, report status, and update project management systems.
Qualifications
University or college degree in a scientific discipline; an advanced degree (Masters, PhD, MD) preferred.
Minimum 2 years of relevant pharmaceutical or scientific experience.
Experience writing medical documents (Phase 1‑3 CSRs, protocols, investigator brochures). 0‑4 years of regulatory writing experience is acceptable based on supervision level.
Strong oral and written communication skills with a high attention to detail.
Ability to work in a team environment, organize time effectively, and demonstrate learning agility.
Knowledge of ICH regulatory guidance and the Medical Writing Style Guide.
Emerging leadership skills in project, process, and time management.
Compensation & Benefits Salary range: $89,000 – $143,750 per year. Expectations include an annual performance bonus and participation in the company’s benefit programs (health, dental, vision, 401(k), paid time off, holiday pay, and other standard benefits). Detailed compensation is tailored by location.
EEO Statement Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, or protected veteran status. We actively seek qualified candidates who are protected veterans and individuals with disabilities.
#J-18808-Ljbffr