6 часов назад
Medical or Life Sciences Data Curator
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Medical or Life Sciences Data Curator (Medical and Scientific Data): Reviewing and summarizing clinical, scientific, pharmaceutical, biotech, and regulatory information for structured weekly monitoring reports with an accent on source verification, evidence-based inclusion decisions, and accurate extraction of study and development details. Focus on identifying meaningful updates, resolving ambiguous or conflicting information, and maintaining consistent records through standardized templates and quality checks.
Location: Fully remote from the Philippines (WFH), night shift
Company
is a tech-enabled workforce augmentation platform connecting businesses with offshore talent and technology.
What you will do
- Review clinical trial registry updates, scientific publications, conference abstracts, pharmaceutical and biotech press releases, regulatory announcements, patent updates, pipeline developments, and drug safety communications.
- Evaluate updates against defined inclusion and exclusion criteria for weekly monitoring reports.
- Extract sponsors, investigational products, indications, study phases, mechanisms of action, regulatory milestones, and other development details.
- Prepare concise, objective summaries supported by the original source.
- Verify facts, flag ambiguous or conflicting information, and perform quality checks on structured records.
Requirements
- Bachelor’s degree in Pharmacy, Nursing, Medical Technology, Biology, Biotechnology, Public Health, Life Sciences, or a related healthcare or scientific field.
- Ability to read and interpret medical or scientific literature and summarize complex information clearly in written English.
- Strong attention to detail, analytical reasoning, fact-checking, and source verification skills.
- Ability to follow detailed guidelines and make evidence-based decisions.
- Experience with structured templates, spreadsheets, or databases.
- Fiber internet with a recommended speed of 100/50 Mbps, backup internet of at least 20 Mbps, and a quiet home workspace are required.
Nice to have
- Experience in clinical research, pharmacovigilance, regulatory affairs, medical writing, clinical data management, or health informatics.
- Familiarity with ClinicalTrials.gov, PubMed, pharmaceutical or biotechnology pipelines, data annotation, or quality review.
- Experience with AI-assisted research and independently verifying outputs against primary sources.
- Wired Ethernet connection and power backup such as a UPS.
Culture & Benefits
- Part-time remote work from home with a supportive, collaborative team.
- Structured onboarding and training.
- Client-specific training for assigned workflows.
- Optional wired Ethernet connection and power backup are preferred for reliable work.
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