Job description

New Moderna Job in MA
  • Description: The Clinical Development team at Moderna is looking for an agile, self-motivated, and experienced individual to serve as an integral part of the Medical Writing Team to support clinical project teams to meet their clinical document deliverables. The successful candidate will be detailed oriented, self-directed and with the ability to be flexible and manage workload to meet project timelines. Here's What You'll Do:
  • Serve as the medical writing Lead contributing to a variety of clinical documents for clinical and regulatory purposes, including clinical protocols, clinical study reports, investigator brochures, and other regulatory submissions documents. Coordinate the efforts of cross-functional teams to produce high-quality, scientifically accurate documents. Plan and coordinate timelines to ensure timely completion of clinical writing projects.
  • Manage timelines and communicate with team stakeholders to maintain awareness of expectations, milestones, and deliverables.
  • Lead significant work streams that involve work across departments or with external vendors.
  • Provide support for QC of complex clinical documents. Here's What You'll Bring to the Table:
  • Minimum of bachelor's degree or equivalent in scientific or medical discipline; Advanced degree preferred.
  • Minimum of six years medical writing experience with a total years of pharmaceutical or biotech experience required.
  • Excellent written communication skills and attention to detail related to consistency, grammar, syntax, and accuracy.
  • Experience producing high quality clinical and regulatory submission documents.
  • Strong project management and organizational skills.
  • Strong organizational/prioritization skills for the management of multiple concurrent projects.
  • Demonstrated proficiency with word processing, spreadsheet, database, presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint) and experience and skill performing medical literature searches.
  • Will work collaboratively with multifunctional teams and partners and will be relentless in pursuing successful outcomes

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About Katalyst Healthcares & Life Sciences

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Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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Frequently asked questions

Q: What skills or qualities help someone succeed as a Medical Writer?

A: To succeed as a Medical Writer, key technical skills include a strong understanding of medical terminology, pharmacology, and regulatory guidelines such as FDA regulations and ICH guidelines. Soft skills like excellent communication, attention to detail, and the ability to distill complex scientific information into clear, concise language are also crucial. These strengths enable Medical Writers to effectively convey critical information to various audiences, from healthcare professionals to patients, and support their career growth by fostering a reputation for accuracy and clarity.

Q: What is the career path for a Medical Writer?

A: A Medical Writer's typical career progression involves starting as an Entry-Level Medical Writer, where they assist in creating content for pharmaceutical companies, medical device manufacturers, or healthcare organizations. As they gain experience, they can move into Mid-Level roles such as Senior Medical Writer or Medical Communications Specialist, where they lead content development, manage teams, and develop strategic communication plans. Ultimately, Senior Medical Writers can advance to roles like Medical Director or Scientific Communications Lead, overseeing large-scale content initiatives and mentoring junior writers, or transition into related fields like Regulatory Affairs, Clinical Research, or Science Publishing.



Katalyst Healthcares & Life Sciences job posting for a Medical Writer in Norwood, MA with a salary of $40 to $66 Hourly with a map of Norwood location.