Senior Medical Writer — Remote (Regulatory/Clinical)

MMS Holdings Inc

Chicago (IL)

Remote

USD 70.000 - 90.000

Vollzeit

14 Tage+

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Zusammenfassung

MMS Holdings Inc is seeking a skilled Medical Writer in Chicago. The successful candidate will have a strong background in regulatory writing, including clinical protocols and study reports. They will ensure quality documentation while mentoring fellow team members and managing project timelines.

Applicants should possess exceptional writing skills and a solid understanding of the pharmaceutical industry. The ideal background includes a degree in a relevant scientific field and experience in leading teams. This role is vital in supporting clinical research and regulatory submissions.

Qualifikationen

  • At least 3-5 years of regulatory writing and clinical medical writing experience.
  • Substantial protocol experience as lead author required.
  • Strong understanding of federal regulations and Good Clinical Practices.

Aufgaben

  • Critically evaluate and analyze medical literature for study design.
  • Write and edit clinical development documents and publications.
  • Interact independently with clients to coordinate projects.

Kenntnisse

Regulatory writing
Clinical study protocol
Exceptional writing skills
Organizational skills
MS Word and Excel expertise
Team leadership

Ausbildung

Bachelors, Masters, or Ph.D. in scientific, medical, or clinical discipline

Tools

MS Word
Excel
PowerPoint

Jobbeschreibung

MMS Holdings Inc is seeking a skilled Medical Writer in Chicago. The successful candidate will have a strong background in regulatory writing, including clinical protocols and study reports. They will ensure quality documentation while mentoring fellow team members and managing project timelines.

Applicants should possess exceptional writing skills and a solid understanding of the pharmaceutical industry. The ideal background includes a degree in a relevant scientific field and experience in leading teams. This role is vital in supporting clinical research and regulatory submissions.

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