Clario, a part of Thermo Fisher Scientific, is hiring an Associate Medical Writer for its Medical Imaging team in India. The role focuses on developing clinical trial documentation, supporting study startup activities, maintaining regulatory and quality records, and coordinating with cross-functional teams to support medical imaging clinical trials.
Candidates with a bachelor’s degree in life sciences, pharmacy, healthcare, clinical research, or a related scientific discipline may be suitable for this opportunity. Medical writing experience is preferred, while equivalent clinical research or scientific documentation experience will also be considered.
Job Details
| Particulars | Details |
|---|---|
| Company | Clario |
| Parent Organization | Thermo Fisher Scientific |
| Job Title | Associate Medical Writer |
| Job Requisition ID | R17975 |
| Location | Bangalore, India; India Remote |
| Employment Type | Full-time |
| Experience | 1+ years of medical writing experience preferred |
| Industry Experience | 2+ years in a relevant industry preferred |
| Department | Medical Imaging |
Position: Associate Medical Writer
The Associate Medical Writer will prepare and maintain study-specific documentation, review clinical protocols and imaging requirements, support compliance activities, and assist with study closeout and document archiving.
Key Responsibilities
- Create, organize, update, and finalize study-specific medical writing and medical communications documents.
- Review study protocols and imaging requirements to understand study procedures and operational requirements.
- Develop Site Manuals, supporting forms, labels, and study-specific communication materials.
- Maintain compliance documentation, including Notes to File, protocol amendment impact assessments, corrections, and quality records.
- Create and maintain source documentation and electronic clinical forms.
- Prepare meeting agendas, minutes, and action items for study startup and project activities.
- Maintain medical communications resources, databases, web content, and document repositories.
- Support project closeout and archive study documentation according to company procedures and regulatory requirements.
- Assist with Standard Operating Procedures (SOPs), Work Instructions, templates, and training materials.
- Maintain study tracking tools, document status reports, and medical writing databases.
- Support project teams with documentation processes, templates, and study documentation requirements.
- Contribute to quality, compliance, efficiency, and continuous improvement initiatives.
Eligibility and Qualifications
Candidates should meet the following preferred criteria:
- Bachelor’s degree in Life Sciences, Biological Sciences, Physical Sciences, Pharmacy, Healthcare, Clinical Research, or a related scientific discipline.
- 1+ years of medical writing experience preferred.
- 2+ years of experience in pharmaceutical, biotechnology, clinical research, healthcare, medical imaging, or related industries preferred.
- Understanding of medical, clinical research, regulatory, or scientific writing principles.
- Knowledge of clinical trial terminology, medical imaging concepts, and clinical research processes preferred.
Equivalent clinical research or scientific documentation experience will also be considered for the medical writing experience requirement.
Required Skills
- Medical Writing: Scientific documentation, proofreading, editing, and document quality review.
- Clinical Research: Clinical trial terminology, study documentation, and clinical research processes.
- Regulatory Documentation: Compliance records, SOPs, Work Instructions, and document archiving.
- Technical Skills: Microsoft Word, Excel, PowerPoint, Outlook, and related productivity tools.
- Communication: Strong written and verbal English communication skills.
- Project Management: Ability to manage multiple projects, priorities, and deadlines.
- Organization: Strong documentation, time-management, and attention-to-detail skills.
- Collaboration: Ability to work independently and coordinate effectively with cross-functional and global teams.
Benefits Offered
Clario lists the following benefits and opportunities:
- Competitive pay and incentives.
- Provident fund and medical insurance.
- Employee programs and local events.
- Modern office spaces and remote work flexibility.
- Professional growth and career development opportunities within a global organization.
Application Details
