Senior Medical Writer — Remote (Regulatory/Clinical)

MMS Holdings Inc; Boston (MA); Remote; USD 80,000 - 110,000; Full time

Job summary

MMS Holdings Inc in Boston is seeking a Medical Writer to evaluate medical literature and prepare clinical documents, including clinical protocols and study reports. This role requires at least 3-5 years of regulatory writing experience in the pharmaceutical industry.

The ideal candidate will possess a Bachelor’s, Master’s, or Ph.D. and exceptional writing and organizational skills. You'll be responsible for mentoring team members and ensuring high-quality submissions to regulatory authorities.

Qualifications

• At least 3-5 years of industry regulatory writing and clinical medical writing experience.
• Substantial clinical study protocol experience, as lead author, required.
• Exceptional writing skills are a must.

Responsibilities

• Critically evaluate and interpret medical literature for study design.
• Write and edit clinical development documents.
• Take ownership of assignments and mentor other writers.

Skills

Regulatory writing

Clinical medical writing

Exceptional writing skills

Project management

Understanding of clinical data

Education

Bachelor's, Master's, or Ph.D. in scientific, medical, clinical discipline

Tools

MS Word

Excel

PowerPoint

Job description

MMS Holdings Inc in Boston is seeking a Medical Writer to evaluate medical literature and prepare clinical documents, including clinical protocols and study reports. This role requires at least 3-5 years of regulatory writing experience in the pharmaceutical industry.

The ideal candidate will possess a Bachelor’s, Master’s, or Ph.D. and exceptional writing and organizational skills. You'll be responsible for mentoring team members and ensuring high-quality submissions to regulatory authorities.