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Full-time
postgraduate degree
Posted 19d ago
~40 hrs/week
Responsibilities
Responsible for authoring and editing scientific manuscripts and publications based on pre-clinical medical device research. This includes transforming complex biological and engineering data into peer-reviewed journals, conference abstracts, and technical communications.
Requirements
Requires an advanced degree in biomedical, life, or health sciences with at least 2 years of medical or scientific writing experience. Candidates must have a proven track record of publishing in journals and a strong understanding of pre-clinical research methods.
Full 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.
ClinChoice is a leading global full & functional service CRO, renowned for its exceptional product development and lifecycle management capabilities across the pharmaceutical, biotechnology, medical device, and consumer health sectors. With three decades of proven expertise and outstanding results, we excel in delivering top-tier services.
Our deep regulatory expertise, clinical trial execution, and robust pharmacovigilance and biometrics capabilities position us as a trusted partner in global markets. ClinChoice proudly maintains a strong presence across the Americas, Europe, and Asia-Pacific, ensuring comprehensive support for our clients worldwide.
Offices: 300 Welsh Road, Building 5, Suite 201, Horsham, Pennsylvania 19044, US
Full-Service CROClinical DevelopmentPost-Marketing & Real-World EvidenceQuality and ComplianceTechnologyConsultingFSP Solution Full-Service SolutionsPharma and BiotechMedical Device and Diagnostics
ClinChoice is a leading global full & functional service CRO, renowned for its exceptional product development and lifecycle management capabilities across the pharmaceutical, biotechnology, medical device, and consumer health sectors. With three decades of proven expertise and outstanding results, we excel in delivering top-tier services.
Our deep regulatory expertise, clinical trial execution, and robust pharmacovigilance and biometrics capabilities position us as a trusted partner in global markets. ClinChoice proudly maintains a strong presence across the Americas, Europe, and Asia-Pacific, ensuring comprehensive support for our clients worldwide.
Offices: 300 Welsh Road, Building 5, Suite 201, Horsham, Pennsylvania 19044, US
Full-Service CROClinical DevelopmentPost-Marketing & Real-World EvidenceQuality and ComplianceTechnologyConsultingFSP Solution Full-Service SolutionsPharma and BiotechMedical Device and Diagnostics