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Company Description ISM Data Technology is dedicated to empowering rural women by delivering world-class data entry, data management, and back-office support solutions to clients worldwide. The organization focuses on bridging the digital divide through sustainable employment opportunities for women in rural communities, while maintaining high standards of accuracy and data security. Its vision is to be a trusted global partner in data management services, combining operational excellence with social impact. Services include data entry and processing, data cleaning and formatting, virtual assistance, and specialized offerings such as invoice processing, e-commerce product listing, and data mining and research. Team members collaborate to provide cost-effective, scalable, and reliable services that foster long-term client relationships built on quality and trust.
Role Description The Clinical Researcher is a full-time, remote role responsible for designing, conducting, and analyzing clinical and healthcare-related studies aligned with the organization’s data-focused services. This role involves developing research protocols, reviewing medical and statistical literature, and ensuring ethical and regulatory compliance in all research activities. The Clinical Researcher will collect, organize, and interpret clinical data, prepare reports, and contribute to publications and presentations that inform evidence-based decision-making. Day-to-day tasks include collaborating with cross-functional teams, communicating research findings to internal and external stakeholders, and supporting data quality initiatives in clinical and healthcare projects. The role also requires maintaining detailed documentation, adhering to timelines, and continuously improving research methodologies and processes.
Qualifications
- Strong analytical skills and experience interpreting complex clinical or health-related data.
- Proficiency in statistics, including study design, data analysis, and use of statistical software tools.
- Solid foundation in medicine or health sciences to understand clinical protocols, outcomes, and terminology.
- Demonstrated research skills, including literature review, protocol development, data collection, and reporting.
- Effective communication skills for presenting findings, writing reports, and collaborating with diverse teams.
- Bachelor’s or Master’s degree in a relevant field (e.g., Medicine, Nursing, Public Health, Biostatistics, Life Sciences, or related discipline).
- Experience with clinical trials, observational studies, or healthcare data projects is an advantage.
- Familiarity with research ethics, regulatory guidelines, and data privacy standards.
- Ability to work independently in a remote setup, manage multiple projects, and meet deadlines.
- Attention to detail, critical thinking, and a commitment to high-quality, accurate work.
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