Medical writer

1886570561

COP $6 a $8 millones

Colombia Bogotá / Otras

Publicado 16 Sep 2025

Investigación / Otras

Vence 19 Oct 2025

IGC PHARMA SAS
Industria de la empresa:
Otros

Descripción general

We are seeking a highly skilled medical writer with expertise in neurology or neuroscience to join our team in developing regulatory documents for submission to the regulatory agencies. The ideal candidate will play a key role in protocol design, literature review, and the preparation of documents supporting proposals for the treatment of neurological and neurodegenerative disorders, with a strong emphasis on Alzheimer’s disease. This role requires the ability to translate complex scientific concepts into clear, compliant documents, ensure thorough integration of current literature, and maintain alignment with global regulatory and industry standards. Key Responsibilities: -Develop innovative and effective protocol designs that meet regulatory requirements and scientific standards. -Conduct comprehensive literature reviews to support protocol development, regulatory submissions, and scientific publications. -Draft, review, and finalize regulatory documents, including INDs, briefing packages, drug designation requests, and submissions to the FDA and international agencies. -Ensure all documents are scientifically accurate, clearly written, and compliant with global regulatory standards. -Serve as the primary point of contact for protocol and study design issues, coordinating with internal teams to resolve them in a timely manner. -Provide regular updates and reports to senior management on study design progress, challenges, and opportunities. -Stay current with scientific and regulatory developments in neurology and neurodegenerative diseases, particularly Alzheimer’s disease, and integrate best practices into study design.

Requisitos para postularse

-Advanced degree (MS, PhD, MD, or PharmD) in basic sciences neurology, neuroscience, pharmacology, psychology or a related life science field. -At least 3-5 years of experience writing and editing scientific publications. -Strong scientific background in neurology and neurodegenerative diseases, especially Alzheimer’s disease. -Excellent scientific writing and communication skills, with the ability to translate complex science into clear, structured documents. -Strong knowledge of regulatory requirements related to study design in clinical research. -Proficiency in MS Word and strong computer skills. -Exceptional attention to detail, strong organizational skills, and ability to manage multiple projects under tight timelines. -Ability to adapt to a fast-paced and dynamic work environment. -Excellent command of written and spoken English.

Datos complementarios

1886570561

Profesional

(Otro) / Otras

Laboratorios farmacéuticos y otros

3 años de experiencia

Contrato Indefinido

1886570561

1 Vacante


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