Senior Medical Writer: Clinical Content & Regulatory Compliance

Syneos Health, Inc.; Buenos Aires; Presencial; ARS 91.385.000 - 137.078.000; Jornada completa

Descripción de la vacante

Syneos Health, Inc. is seeking a Medical Writer to translate clinical and scientific data into clear, evidence-based content.

You will collaborate with internal teams to ensure strategic alignment, scientific rigor, and quality across publications and educational materials. Responsibilities include researching literature with PubMed, developing and coordinating medical writing deliverables, supporting clinical study protocols and amendments, and ensuring compliance with regulatory standards.

Formación

• BS + 8 yr experience; MSc/M. Pharm/PharmD + 4 yr experience; PhD + 1 yr experience
• 3-4 years of clinical research experience
• Working knowledge of Microsoft Office software (Word, Excel, and PowerPoint)
• Working knowledge of medical literature databases (e.g., Ovid, Medline, PubMed, etc.)

Responsabilidades

• Research and Analysis – Gather and evaluate scientific literature; validate references.
• Content Development – write and edit medical writing deliverables; ensure clarity.
• Clinical Study Protocol – Support protocols, reports, NDA/eCTD submissions; abstracts and presentations.
• Quality Assurance – Ensure scientific accuracy and QA; support MLR processes and peer review.

Conocimientos

Scientific and clinical writing

Literature searching

Quality control

Stakeholder management

MS Office & databases

Compliance knowledge

Advanced English communication

Educación

BS + 8 yrs exp; MSc/M.Pharm/PharmD + 4 yrs exp; PhD + 1 yr exp

3-4 yrs clinical research experience

Herramientas

Microsoft Office

Medical literature databases

Descripción del empleo

Syneos Health, Inc. is seeking a Medical Writer to translate clinical and scientific data into clear, evidence-based content.

You will collaborate with internal teams to ensure strategic alignment, scientific rigor, and quality across publications and educational materials. Responsibilities include researching literature with PubMed, developing and coordinating medical writing deliverables, supporting clinical study protocols and amendments, and ensuring compliance with regulatory standards.