Remote Senior Medical Writer - Regulatory Submissions Lead

mmsholdingsinc; Ciudad de México; A distancia; MXN 600.000 - 900.000; Jornada completa

Descripción de la vacante

MMS Holdings Inc. is seeking an experienced Medical Writer to join our remote team in Mexico. The role focuses on critical literature evaluation and the creation of comprehensive regulatory writing documents for clinical development.

Ideal candidates will have 3+ years in pharma, strong writing skills, and experience leading project teams under tight timelines. Remote-based work within Mexico is offered with opportunities to collaborate globally.

Formación

• 3+ years of pharmaceutical industry experience.
• Expertise in regulatory writing and clinical medical writing.
• Experience leading and managing teams with tight timelines.
• Strong scientific writing and communication skills.

Responsabilidades

• Critically evaluate literature to select primary resources for study design and regulatory reporting.
• Write/edit clinical development documents (protocols, investigator brochures, study reports, consent forms).
• Prepare safety/efficacy summaries and regulatory modules.
• Meet timelines and manage writing workflows.
• Mentor writers and project team members.
• Coordinate with clients to manage projects and deliverables.

Conocimientos

Regulatory writing

Team leadership

Clinical writing

Medical writing

Educación

Bachelor's/Master's/PhD in scientific/medical/clinical discipline

Herramientas

MS Word

MS Excel

PowerPoint

Descripción del empleo

MMS Holdings Inc. is seeking an experienced Medical Writer to join our remote team in Mexico. The role focuses on critical literature evaluation and the creation of comprehensive regulatory writing documents for clinical development.

Ideal candidates will have 3+ years in pharma, strong writing skills, and experience leading project teams under tight timelines. Remote-based work within Mexico is offered with opportunities to collaborate globally.