Senior Associate, Medical Writing

ClinChoice; Pasig; On-site; PHP 600,000 - 1,000,000; Full time

Job summary

ClinChoice is seeking a skilled Medical Writer to author and edit manuscripts based on pre-clinical studies of medical devices. You will transform complex biomechanical and biomedical data into publication-ready documents, including journal papers and conference abstracts.

The role requires an advanced degree and at least two years in medical writing, with strong English writing skills and familiarity with GDP and publication standards.

Qualifications

• Advanced degree in biomedical sciences, life sciences, biomedical engineering, or health sciences.
• At least 2 years of medical writing or publication experience.
• Experience publishing studies in peer or non-peer reviewed journals.
• Medical device experience preferred.
• Proficient in Microsoft Office (Word, Excel, PowerPoint).
• Strong understanding of pre-clinical research methods.
• Proficient in oral and written English.

Responsibilities

• Author and edit scientific manuscripts describing pre-clinical medical devices studies.
• Develop publication deliverables including journal manuscripts, abstracts, posters and presentations.
• Review protocols, reports, statistics, and data summaries for accuracy.
• Synthesize evidence into clear, publication-ready narratives.
• Coordinate manuscript development with cross-functional teams.

Skills

English language proficiency

Scientific writing

Communication skills

Education

MS/PhD in biomedical sciences or related

Tools

Microsoft Word

Excel

PowerPoint

Job description

This role is responsible for authoring, editing, and coordinating scientific manuscript and related publications based on pre-clinical research involving medical devices. This role transforms complex scientific, engineering, and biological data into scientific manuscripts which may include peer-reviewed publications, conference abstracts, or technical communications that accurately represent study findings and comply with applicable scientific, ethical, and publication standards.

Primary Responsibilities

• Author and edit scientific manuscripts describing pre-clinical medical devices studies including in vitro studies, bench testing studies, biocompatibility studies, animal studies, human factors and usability studies, performance and proof-of-concept evaluations
• Develop publication deliverables including peer-reviewed journal manuscripts, conference abstracts, and posters and presentations.
• Review study study protocols, reports, statistical outpus, and raw data summaries.
• Synthesize scientific evidence into clear, logical, and publication-ready narrative.
• Collaborate with subject matter expert/s to interpret findings and validate scientific conclusions.
• Conduct targeted literature searches to support manuscript development.
• Evaluate scientific publications and relevant standards applicable to medical devices.
• Prepare background section, literature reviews, and discussion content.
• Coordinate manuscript development with cross-functional teams.
• Ensure compliance with GDP, journal-specific author guidelines, ethical publication standards, and company quality procedures.

Minimum Qualifications

• Advanced degree (e,g., MS, PhD, PharmD, MD, or equivalent) in biomedical sciences, life sciences, biomedical engineering, or health sciences.
• At least 2 years of medical writing, scientific writing, or publication experience.
• Experience in publishing studies in peer or non-peer reviewed journals required.
• Medical device experience preferred.
• Proficient in Microsoft Office suites (e,g,, Word, Excel, PPT)
• Strong understanding of pre-clinical research methods.
• Proficient in oral and written English language.
• Good analytical and comprehension skills.