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Manager, Medical Editor, Medical Writing Operations

Employer
Moderna, Inc.
Location
Cambridge, MA
Start date
Jan 26, 2023

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Job Details

The Role:

The Medical Writing Operations team at Moderna is looking for an agile, self-motivated individual to serve as a Manager, Medical Editing, Medical Writing Operations. This individual will be responsible to edit, format, and perform full content QC checks of medical writing deliverables and provide support to the Medical Writing Operations team. The Manager takes a lead role in planning and resourcing work within the Medical Editing group, provides guidance and supervision to the Medical Editors, and helps improve the QC review process. The successful candidate will be detailed oriented, self-directed, and with the ability to be flexible and manage workload to meet project timelines.

Heres What Youll Do:

  • Supervise day-to-day performance of the Medical Editing function within Medical Writing Operations.

  • Support the head of Medical Writing Operations in planning, resourcing, and scheduling documents for QC review.

  • Collaborate with the Medical Writing Operations group to continually improve and refine the QC review process.

  • Perform QC review of clinical and regulatory documents for submission to regulatory agencies in accordance with company-specific SOPs, templates, style guide, and QC processes, within established timelines.

  • Provide editorial and formatting support, with a focus on clarity, accuracy, and consistency, and ensure that format and content comply with applicable regulations.

  • Ensure that the format and content of clinical and regulatory documents comply with applicable submission formatting regulations.

  • Assist in the review, development, implementation, and maintenance of documents related to QC (eg, templates, work instructions, standard operating procedures, job aids, QC checklists, as needed).

  • Identify and appropriately communicate risks associated with document QC and propose mitigation plans.

  • Collaborate with members of the Medical Writing team to ensure that QC findings are addressed appropriately.

  • Attend project-related meetings.

  • Complete project-specific and company training, as assigned.

Heres What Youll Bring to the Table:

  • Bachelors degree required. Life science or related allied health field preferred.

  • Minimum of 5 years of document QC experience in the biopharmaceutical industry, with at least 1 year of supervisory experience.

  • Working knowledge of GCP, FDA regulations, ICH guidelines (in particular ICH E3, E6, and E9)., and the drug development process.

  • Familiarity with clinical study and submission documents such as protocols, Investigator Brochures, and CSRs.

  • Able to accurately interpret data and express findings in a clear and concise written manner.

  • Project/time management and organizational skills, as well as the ability to work independently.

  • Flexibility in meeting challenging deadlines and changing requirements while working on multiple projects.

  • Comprehensive Microsoft Office, especially Word but also PowerPoint and Excel skills. Experience working in a Veeva environment preferred.

  • Ability to communicate with professionals from a variety of backgrounds.

  • Attention to detailstyle, consistency, grammar, syntax, scientific accuracy

Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:

  • Highly competitive and inclusive medical, dental and vision coverage options
  • Flexible Spending Accounts for medical expenses and dependent care expenses
  • Lifestyle Spending Account funds to help you engage in personal enrichment and self-care activities
  • Family care benefits, including subsidized back-up care options and on-demand tutoring
  • Free premium access to fitness, nutrition, and mindfulness classes
  • Exclusive preferred pricing on Peloton fitness equipment
  • Adoption and family-planning benefits
  • Dedicated care coordination support for our LGBTQ+ community
  • Generous paid time off, including:
    Vacation, sick time and holidays
    Volunteer time to participate within your community
    Discretionary year-end shutdown
    Paid sabbatical after 5 years; every 3 years thereafter
  • Generous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents
  • 401k match and Financial Planning tools
  • Moderna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit options
  • Complimentary concierge service including home services research, travel booking, and entertainment requests
  • Free parking or subsidized commuter passes
  • Location-specific perks and extras!

Candidates should be aware that Moderna currently maintains a policy requiring all US-based employees to be fully vaccinated against COVID-19 and receive a booster shot once eligible. Newly hired employees must be vaccinated and boosted prior to their employment start date. Moderna is an equal opportunity employer and will provide a reasonable accommodation to those unable to be vaccinated or receive a booster where it is not an undue hardship to the company to do so as provided under federal, state, and local law.

About Moderna

In over 10 years since its inception, Moderna has transformed from a research-stage company advancing programs in the field of messenger RNA (mRNA), to an enterprise with a diverse clinical portfolio of vaccines and therapeutics across seven modalities, a broad intellectual property portfolio in areas including mRNA and lipid nanoparticle formulation, and an integrated manufacturing plant that allows for rapid clinical and commercial production at scale. Moderna maintains alliances with a broad range of domestic and overseas government and commercial collaborators, which has allowed for the pursuit of both groundbreaking science and rapid scaling of manufacturing. Most recently, Moderna's capabilities have come together to allow the authorized use and approval of one of the earliest and most effective vaccines against the COVID-19 pandemic.

Moderna's mRNA platform builds on continuous advances in basic and applied mRNA science, delivery technology and manufacturing, and has allowed the development of therapeutics and vaccines for infectious diseases, immuno-oncology, rare diseases, cardiovascular diseases and autoimmune diseases. Moderna has been named a top biopharmaceutical employer by Science for the past seven years. To learn more, visit www.modernatx.com.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Moderna will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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Company

Moderna is advancing messenger RNA (mRNA) science to create a new class of transformative medicines for patients. Moderna’s platform builds on continuous advances in basic and applied mRNA science, delivery technology and manufacturing, providing the Company the capability to pursue in parallel a robust pipeline of new development candidates. Moderna is developing therapeutics and vaccines for infectious diseases, immuno-oncology, rare diseases and cardiovascular diseases, independently and with strategic collaborators.

mRNA is now a turning point in the history of science, medicine, technology, even humankind itself. With this breakthrough discovery, many of the world’s biggest and most challenging medical problems are no longer a question of “how?” but merely a question of “when?”

Come with us as we pursue the uncharted reaches of possibility and make your mark on the future of medicine.

 

Stock Symbol:

MRNA  

Stock Exchange:

USNASDAQ GS

 

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Company info
Website
Phone
617-714-6500
Location
200 Technology Square
Cambridge, MA
United States

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