- Assist in the execution of clinical research studies and related research activities.
- Support patient recruitment, screening, follow-up, and other study-related activities.
- Assist with the collection, recording, and management of clinical data while ensuring accuracy and adherence to study protocols.
- Coordinate with cross-functional teams to support the smooth execution of research projects.
- Assist in monitoring and tracking study progress and report any issues or deviations to the relevant team members.
- Support study investigators and site staff during research activities and patient interactions.
- Assist in preparing project updates, reports, and research documentation.
- Support the preparation and maintenance of regulatory and study-related documents.
- Follow clinical research protocols, guidelines, and standard operating procedures.
- Maintain accurate records while ensuring the confidentiality and security of patient and research data.
- Participate in field-based research activities as required.
- Bachelor’s/Master’s degree in Optometry or an equivalent Optometry qualification is mandatory.
- Freshers are welcome; candidates with academic projects, internships, or exposure to clinical research will be preferred.
- Basic understanding of optometry and clinical research processes.
- Good communication and interpersonal skills, with the ability to interact confidently with patients and study teams.
- Strong attention to detail and organizational skills.
- Ability to work independently as well as collaboratively in a team environment.
- Willingness to participate in field-based research activities.
- Basic proficiency in MS Office and data management tools.
- Strong interest in clinical research and willingness to learn.
Skills Required
- Freshers or candidates with relevant internship or academic exposure to clinical research
- Basic understanding of clinical research processes and guidelines
- Good communication and interpersonal skills
- Strong attention to detail and organizational skills
- Ability to work independently and in a team environment
- Proficiency in MS Office and basic data management tools
- Passion for clinical research and willingness to learn
What We Do
Remidio is an innovative ISO 13485 certified medical device company that seeks to create Healthcare Access by combining the simplicity of product design with cutting edge technology and sustainable business model innovations. Remidio uses principles of Design Thinking and involves key stakeholders during the product development process – clinicians, patients, and health workers, with a view to designing product solutions that are simple to use, clinically relevant, reliable, and scalable. Remidio’s CE marked and FDA 510k registered retinal imaging devices have helped screen and impact more than 7.5 million patients in 15 countries globally, as a result of increased access provided by the ease of use and affordability of Remidio’s patented optics on the smartphone platform.


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