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Analyst II, Medical Writing, Immunology Job at Johnson & Johnson Innovative Medi

Analyst II, Medical Writing, Immunology Job at Johnson & Johnson Innovative Medi

MediabistroSpring House, PA, United States
6 days ago
Job type
  • Full-time
Job description

Overview

Analyst II, Medical Writing, Immunology role at Johnson & Johnson Innovative Medicine. This role is available across multiple locations and may be posted under different requisition numbers to comply with local requirements. Remote work options may be considered on a case-by-case basis and if approved by the Company.

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.

Learn more at https : / / www.jnj.com / innovative-medicine

You Will Be Responsible For

  • Writes and coordinates basic clinical documents such as, but not limited to, Phase 1 protocols, Phase1 / 2 CSRs, table of studies, narratives, and initial IBs.
  • Writes, contributes to, and / or coordinates low to medium complexity clinical and regulatory documents such as, but not limited to, Phase 2 / 3 CSRs and protocols, IB updates, summary documents, and regulatory responses under supervision.
  • Performs document QC, completes lists of abbreviations or references, conducts literature searches, and performs other basic tasks with supervision as needed.
  • Participates in and may lead cross-functional document planning and review meetings. Works in a team environment with some guidance while increasing independence for longer-term activities.
  • Takes an active role on assigned projects with respect to timing, scheduling, and tracking.
  • Interacts with cross-functional colleagues on document content and champions MW processes and best practices. Responsible for establishing document timelines and strategies in accordance with internal processes, with some mentorship from functional management and clinical team, as needed.
  • In accordance with experience level : guides or trains cross-functional team members on processes and best practices; leads early- or late-stage compound writing teams with supervision, as required.
  • Learns and adheres to SOPs, templates, best practices, policies, Medical Writing Style Guide.
  • Regularly meets with manager and mentors and attends departmental meetings; attends cross-functional meetings as appropriate (e.g., project kick-off and review meetings, study team meetings, Global Program Team meetings).
  • Completes all time reporting, training, and metrics database and project tracking updates as required in relevant company systems.
  • Maintains and applies knowledge of industry, company, and regulatory guidelines.

Qualifications / Requirements

  • Education : A university / college degree in a scientific discipline is required. An advanced degree (e.g., Masters, PhD, MD) is preferred.
  • Skills / Experience

  • A minimum of 2 years of relevant pharmaceutical / scientific experience is required.
  • A range of 0 to 4 years of regulatory medical writing experience is required, depending on tasks performed and level of supervision needed.
  • Strong oral and written communication skills.
  • Attention to detail and ability to function in a team environment.
  • Organizes time well and demonstrates learning agility.
  • Builds solid and productive relationships with cross-functional team members.
  • Gains experience in interpreting, summarizing, and presenting statistical and medical information to ensure quality and accuracy of content with supervision.
  • Emerging leadership skills in project and process management as well as time management; resolves basic problems independently and more complex problems with supervision.
  • Develops and applies knowledge of regulatory guidance documents such as ICH requirements.
  • The expected pay range for this position is $89,000 to $143,750. The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. Bonuses are awarded at the Company’s discretion on an individual basis.

    Employees and / or eligible dependents may be eligible to participate in company-sponsored benefit programs such as medical, dental, vision, life insurance, disability, and other programs. Eligible employees may participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

    Time Off Benefits

  • Vacation - up to 120 hours per calendar year
  • Sick time - up to 40 hours per calendar year; for employees in Washington state - up to 56 hours
  • Holiday pay, including Floating Holidays - up to 13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year
  • For additional general information on company benefits, please go to : https : / / www.careers.jnj.com / employee-benefits

    The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.

    This job posting is anticipated to close on September 19, 2025. The Company may extend this time period, in which case the posting will remain available on https : / / www.careers.jnj.com to accept additional applications.

    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, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. If you are an individual with a disability and would like to request an accommodation, please contact us via https : / / www.jnj.com / contact-us / careers.

    Important notices

    Referrals increase your chances of interviewing at Johnson & Johnson Innovative Medicine by 2x. Sign in to set job alerts for “Medical Analyst” roles.

    Location notes : Titusville, NJ; job postings also reference other locations. Salary listed reflects the US location.

    This description contains the core responsibilities and qualifications for the Analyst II, Medical Writing, Immunology role and does not include every duty that may be assigned.

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