Clario has announced an opportunity for candidates interested in medical writing, clinical research and medical imaging. The full-time position is listed for Bangalore, India and India Remote and provides an opportunity to work on scientific and operational documentation supporting medical imaging clinical trials.
The Clario Associate Medical Writer job involves developing and maintaining clinical study documentation, reviewing protocols and imaging requirements, supporting study startup, preparing compliance documentation and collaborating with global cross-functional teams.
Candidates with bachelor’s degrees in Life Sciences, Biological Sciences, Physical Sciences, Pharmacy, Healthcare, Clinical Research or related scientific disciplines are preferred. Candidates with medical writing experience or equivalent clinical research/scientific documentation experience may be considered.
About Clario
Clario provides endpoint data solutions to the clinical trials industry and supports life sciences companies in generating clinical evidence.
Its capabilities cover medical imaging, electronic Clinical Outcome Assessments (eCOA), precision motion, cardiac solutions and respiratory endpoints.
According to the employer’s job description, Clario’s technologies and scientific expertise have supported thousands of clinical trials across more than 100 countries.
This Associate Medical Writer position at Clario specifically supports the Medical Imaging team and combines medical writing with clinical research operations, study documentation and imaging sciences.
Key Responsibilities
As an Associate Medical Writer at Clario, the selected candidate will support clinical study documentation throughout study startup and execution.
Responsibilities include:
- Create, organize and maintain study-specific Medical Writing and Medical Communications documentation.
- Support clinical study startup documentation activities.
- Review study protocols and imaging requirements to accurately interpret study procedures, schedules and operational requirements.
- Create, update and finalize Site Manuals, supporting forms, labels and study-specific communication materials.
- Prepare and maintain compliance-related documentation.
- Develop Notes to File, protocol amendment impact assessments, corrections and other quality records.
- Create and maintain source documentation and electronic clinical forms.
- Prepare meeting agendas, meeting minutes and action-item documentation.
- Participate in internal and external meetings covering study startup, documentation and compliance activities.
- Maintain Medical Communications resources, databases, web content and document repositories.
- Support project closeout and appropriate archiving of study documentation.
- Assist with developing and maintaining Standard Operating Procedures (SOPs) and Work Instructions.
- Review and update templates, training materials and educational resources.
- Support reader training materials and study-specific training content.
- Maintain study tracking tools, document status reports and Medical Writing databases.
- Guide project teams on documentation processes, templates and requirements.
- Contribute to continuous improvement initiatives related to quality, compliance and operational efficiency.
Qualification & Eligibility
Clario lists a bachelor’s degree in a relevant scientific or healthcare discipline as preferred.
Suitable educational backgrounds specified by the employer include:
Bachelor’s Degree in Life Sciences / Biological Sciences / Physical Sciences / Pharmacy / Healthcare / Clinical Research or a related scientific discipline.
For Indian candidates, this may correspond to relevant degrees such as:
B.Pharm, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Clinical Research and other relevant biological, physical science or healthcare degrees, subject to Clario’s screening criteria.
Candidates with relevant higher qualifications such as M.Pharm or M.Sc in a related life-science/scientific discipline may also be academically aligned with the role, although the job posting specifically states a bachelor’s degree as the preferred educational requirement.
Experience Required
Clario lists experience requirements as preferred rather than explicitly mandatory.
The employer specifies:
- 1+ year of medical writing experience preferred.
- Equivalent clinical research or scientific documentation experience will be considered.
- 2+ years of experience in pharmaceutical, biotechnology, clinical research, healthcare, medical imaging or a related industry preferred.
Therefore, this position should not be advertised as a pure fresher role.
Candidates with at least one year of medical writing experience or relevant scientific/clinical documentation exposure would be more closely aligned with the stated profile.
Key Skills Required
Candidates should have knowledge or proficiency in:
- Medical Writing
- Scientific Writing
- Clinical Research
- Clinical Trial Documentation
- Medical Imaging Documentation
- Study Startup
- Protocol Review
- Site Manuals
- Scientific Documentation
- Regulatory Documentation
- SOPs & Work Instructions
- Document Control
- Proofreading & Editing
- Quality Review
- Source Documentation
- Clinical Forms
- Meeting Minutes
- Study Tracking
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Microsoft Outlook
Strong English written and verbal communication skills are important for this role.
Candidates should also demonstrate excellent attention to detail, proofreading ability, organizational skills, time management and the ability to handle multiple projects and deadlines.
Who Should Apply?
This Clario Associate Medical Writer job may be particularly suitable for candidates who have:
- A relevant life science, pharmacy, healthcare or clinical research degree.
- Previous medical or scientific writing experience.
- Clinical research documentation experience.
- Experience preparing or reviewing study-related documents.
- Understanding of clinical trial terminology.
- Exposure to medical imaging concepts.
- Strong proofreading and editing capabilities.
- Experience working according to SOPs and quality standards.
- Strong Microsoft Office skills.
Candidates with clinical research or scientific documentation experience but without the exact “Medical Writer” designation may also consider applying because the employer explicitly states that equivalent experience will be considered.
Benefits at Clario
According to the official job posting, Clario offers:
- Competitive pay and incentives.
- Provident fund.
- Medical insurance.
- Employee engagement programs and local events.
- Modern office facilities.
- Remote-work flexibility.
- Professional growth opportunities.
- Career development within a global organization.
The position also provides exposure to international clinical research and medical imaging projects.
Why Consider This Medical Writing Role?
The Associate Medical Writer role at Clario differs from a purely publication-focused medical writing position.
The responsibilities are closely connected to clinical trial operations and medical imaging, including protocol review, Site Manuals, study forms, compliance documentation, SOPs, training content and study tracking.
This can make the opportunity particularly relevant for professionals seeking to build careers at the intersection of medical writing, clinical research operations and medical imaging.
Estimated Salary
Clario has not disclosed compensation for this vacancy.
For editorial purposes, a realistic estimated market range for an Associate Medical Writer with relevant experience in India may be approximately:
₹4,50,000 – ₹8,00,000 per year
This is an editorial market estimate and not an official salary disclosed by Clario. Actual compensation may vary based on medical writing experience, clinical research exposure, skills, current compensation and the employer’s internal salary structure.
How to Apply
