Kannada Bhavan Karnataka Part time content writer Jobs – 24 Open Jobs Today

Associate Medical Writer
Clario —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
3d
Content Writer Intern
AppsForBharat —Bengaluru, Karnataka
- ₹20,000 - ₹25,000 a month
- English
- In-person
- Internship
Technical Content Writer
Apeiron Global Pvt. Ltd —Bengaluru, Karnataka
- Part-time
- Remote
- Writing skills
- English
- Research
Associate Technical Writer : 19887
Whatfix —Bengaluru, Karnataka
- Bachelor's degree
- APIs
- Leadership
- Commuter assistance
- Health insurance
Quick apply
13d
Copy/Content Writer
Lollypop —Bengaluru, Karnataka
- Full-time
- AI
- Internship
- Communication skills
Content Writer
Mediacle Technologies LLP —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Writing skills
- English
Assistant Manager - Editorial
Emeritus Institute of Management —Bengaluru, Karnataka
- Writing skills
- English
- Master's degree
(Intern) Content writer
BrandStory —Bengaluru, Karnataka
- Full-time
- English
- Research
Technical Writer
Siemens Gamesa —Bengaluru, Karnataka
- Full-time
- Bachelor's degree
- Manufacturing
- Editing
copywriter
CRED —Bengaluru, Karnataka
- Full-time
- Health insurance
- Paid sick time
Assistant Manager - Content
Emeritus Institute of Management —Bengaluru, Karnataka
- Writing skills
- English
- Master's degree
Medical Writer II
CELEGENCE —Bengaluru, Karnataka
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Staff Technical Writer
Okta —Bengaluru, Karnataka
- Writing skills
- Master's degree
- Bachelor's degree
Content Writer ( CW )
GA Software Technologies —Bengaluru, Karnataka
- Email
- Communication skills
Senior Technical Writer
Okta —Bengaluru, Karnataka
- Writing skills
- Engineering
- Bachelor's degree
Senior Content Copywriter - Astro
AppsForBharat —Bengaluru, Karnataka
- English
- Research
Marketing - Content & Growth Associate
PromptCloud Technologies Pvt Ltd —Bengaluru, Karnataka
- Online application
- Remote
- AI
- Communication skills
- Flexible schedule
Quick apply
13d
Senior Content Manager
Indiahikes —Bengaluru, Karnataka
- Full-time
Senior Medical Writer
CELEGENCE —Bengaluru, Karnataka
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Medical Writer
Navitas Life Sciences —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Medicine

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Associate Medical Writer

Clario -
Bengaluru, Karnataka

Apply Now

Job details

Full-time
3 days ago

Benefits

Provident Fund
Health insurance

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Outlook
Clinical research
English
Microsoft Office
Bachelor's degree
Clinical trials
Proofreading
Medical imaging
Communication skills
Editing
Time management

Full job description

Join Clario, a part of Thermo Fisher Scientific and help advance medical imaging clinical trials through the delivery of high-quality scientific and operational documentation. As an Associate Medical Writer within our Medical Imaging team, you will play an important role in supporting study startup activities, developing clinical trial documentation, maintaining quality and compliance standards, and partnering with cross-functional teams to ensure successful study execution. This position offers an excellent opportunity to build expertise in medical writing, clinical research operations, and imaging sciences while contributing to studies that support life-changing therapies worldwide.

What We Offer

Competitive pay and incentives.
Provident fund and medical insurance.
Engaging employee programs and local events.
Modern office spaces and remote work flexibility.
Opportunities for professional growth and career development within a global organization.

What You'll Be Doing

Support study startup activities by creating, organizing, and maintaining study-specific Medical Writing and Medical Communications documentation.
Review study protocols and imaging requirements to ensure accurate interpretation of study procedures, schedules, and operational requirements.
Create, update, and finalize study documentation, including Site Manuals, supporting forms, labels, and study-specific communication materials.
Develop, review, and maintain compliance-related documentation, including Notes to File, protocol amendment impact assessments, corrections, and other quality records as required.
Create and maintain source documentation and electronic clinical forms to support study execution and operational requirements.
Prepare meeting agendas, meeting minutes, and action item documentation for study startup, project, and Medical Communications activities.
Attend internal and external meetings related to study startup documentation, compliance activities, and operational deliverables.
Support the maintenance and enhancement of Medical Communications resources, databases, web content, and document repositories.
Assist with project closeout activities and ensure study documentation is archived in accordance with company procedures and regulatory requirements.
Support the development, review, and maintenance of Standard Operating Procedures (SOPs), Work Instructions, templates, and training materials.
Assist with the review and update of reader training materials, study training content, and educational resources.
Maintain study tracking tools, document status reports, and Medical Writing databases to ensure accurate reporting and document control.
Provide guidance and support to project teams regarding document development processes, templates, and study documentation requirements.
Contribute to continuous improvement initiatives focused on quality, compliance, efficiency, and operational excellence.

What We Look For

Bachelor's degree in Life Sciences, Biological Sciences, Physical Sciences, Pharmacy, Healthcare, Clinical Research, or a related scientific discipline preferred.
1+ years of medical writing experience preferred, although equivalent clinical research or scientific documentation experience will be considered.
2+ years of experience within 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.
Strong proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, Outlook, and related productivity tools.
Excellent written and verbal communication skills with the ability to communicate effectively in English.
Strong attention to detail with exceptional proofreading, editing, and document quality review skills.
Demonstrated ability to manage multiple projects, priorities, and deadlines simultaneously.
Strong organizational, documentation, and time management skills.
Ability to work independently while collaborating effectively within cross-functional and global teams.
Adaptability and flexibility in managing changing priorities within a fast-paced environment.
Professional, proactive, and customer-focused approach with a commitment to quality and continuous improvement.

At Clario, a part of Thermo Fisher Scientific, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Apply Now

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part time content writer jobs in kannada bhavan karnataka

Associate Medical Writer

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Staff Technical Writer

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