What are the responsibilities and job description for the Medical Writer (Remote) position at Mabaya group?
Role Description:
Mabaya Group is looking for a detail-oriented and knowledgeable Medical Writer to produce high-quality medical and scientific content. The ideal candidate will have a strong background in medical writing, the ability to translate complex scientific data into clear and engaging materials, and experience working on regulatory documents, clinical studies, or healthcare communications.
This is a part-time contract role, fully remote, but candidates must be based in Chicago, Illinois, and authorized to work in the U.S.
Responsibilities:
- Write, edit, and proofread medical and scientific content, including regulatory documents, clinical study reports, journal articles, and white papers.
- Ensure all materials are scientifically accurate, evidence-based, and compliant with industry guidelines.
- Conduct in-depth research to support content development and validate information from credible sources.
- Work closely with healthcare professionals, researchers, and regulatory teams to develop high-quality materials.
- Maintain compliance with medical writing standards, such as AMA, ICMJE, and GPP guidelines.
- Manage multiple projects while meeting tight deadlines and ensuring content clarity.
Qualifications:
Minimum Requirements:
- 3 years of experience as a medical writer, scientific writer, or in a similar role.
- Bachelor’s or advanced degree in life sciences, medicine, pharmacy, or a related field (MD, PhD, PharmD, MS preferred).
- Strong understanding of clinical research, medical terminology, and scientific publications.
- Ability to simplify complex medical topics for diverse audiences, including healthcare professionals and the public.
- Excellent grammar, editing, and research skills.
- Candidates must be based in Chicago, Illinois, and authorized to work remotely in the U.S.
Preferred Skills:
- Experience with regulatory writing, medical communications, or clinical trial documentation.
- Familiarity with FDA, EMA, and ICH guidelines.
- Proficiency in medical writing software and reference management tools.
- Strong collaboration skills to work with multidisciplinary teams.
Compensation & Job Type:
- Part-Time, Contract (Paid) – Compensation is project-based or hourly, depending on experience.
- Estimated Salary Range: $30– $50 per hour, based on expertise and project complexity.
- Remote – Candidates must be based in Chicago, Illinois, and authorized to work within U.S. time zones.
- Travel Requirements: None.
Salary : $30 - $50
