bangalore city bengaluru karnataka medical writer Jobs – 26 Open Jobs Today

Medical Writer
Novo Nordisk —Bengaluru, Karnataka
- Doctoral degree
- Writing skills
- English
11h
2500_ Medical Writer
Recruise —Bengaluru, Karnataka
- Full-time
Quick apply
Medical Writer - Manager
Annalect, Omnicom Media Group India Private Limited. —Bengaluru, Karnataka
- Doctoral degree
- Organizational skills
- Communication skills
- Health insurance
5d
Medical Writer
Dr. Kamini Rao Hospitals (Medline Academics) —Bengaluru, Karnataka
- ₹25,000 - ₹60,000 a month
- Part-time
- Medicine
- Writing skills
- English
Quick apply
Regulatory Medical Writer
Remidio —Bengaluru, Karnataka
- Bachelor's degree
- Communication skills
- Time management
Sr Safety Medical Writer
Novo Nordisk —Bengaluru, Karnataka
- Doctoral degree
- English
- Master's degree
Medical Writer - Senior Executive
Annalect, Omnicom Media Group India Private Limited. —Bengaluru, Karnataka
- Microsoft Word
- Word processing
- Project management
- Health insurance
5d
Lead Medical Writer
Healthminds Consulting —Bengaluru, Karnataka
- Full-time
- Medicine
- Doctoral degree
- Master's degree
4h
1700_SR Medical Writer
Recruise —Bengaluru, Karnataka
- Full-time
- Project management
- Time management
Quick apply
Technical Writer
Philips —Bengaluru, Karnataka
- Full-time
- English
- Bachelor's degree
- Electrical Engineering
5d
Medical Writer/ Senior Medical Writer
MS CLINICAL —Bengaluru, Karnataka
- Full-time
- Medicine
- Doctoral degree
- Research
- Health insurance
Senior Scientific Writer – Contract
Healthminds Consulting —Bengaluru, Karnataka
- Full-time
- Remote
- Research
- In-person
4h
Senior Medical Writer
Healthminds Consulting —Bengaluru, Karnataka
- Full-time
- Medicine
- Doctoral degree
- Writing skills
- Health insurance
Medical Communication Writer
Healthminds Consulting —Bengaluru, Karnataka
- Full-time
- Writing skills
- Research
- Master's degree
Medical Tagging / Writing
Healthminds Consulting —Bengaluru, Karnataka
- Full-time
- Doctoral degree
- Master's degree
- Project management
- Health insurance
Senior Medical Writer
CELEGENCE —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Medical Writer
Navitas Life Sciences —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Medicine
Associate Director, Medical Writing
GlaxoSmithKline —Bengaluru, Karnataka
- Full-time
- Doctoral degree
- Master's degree
- Project management
12d
Lead Expert - Scientific Writer
Merck Group —Bengaluru, Karnataka
- Full-time
- Medicine
- English
- Analysis skills
Regulatory Analyst - Clinical Affairs
Remidio —Bengaluru, Karnataka
- Bachelor's degree
- Communication skills
- Time management

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Medical Writer

Novo Nordisk -
Bengaluru, Karnataka

Apply Now

Job details

11 hours ago

Qualifications

Doctoral degree
Writing skills
English
Master's degree
Analysis skills
Project management
Continuous improvement

Full job description

Medical Writer

Category: Clinical Development

Location: Bangalore, Karnataka, IN

Team: Clinical Reporting

Location : Bangalore, Novo Nordisk Global Business Services (GBS), India

Your New Role

As a Medical Writer, you will perform a wide range of medical writing tasks to support clinical development programs, delivering high-quality content and documents that align with the Clinical Reporting strategy. The tasks for trial and/or non-trial activities within clinical reporting will include but will not be limited to preparation of Protocols, Clinical Trial Reports (CTRs), Investigator Brochure (IB), CTD Module 2 summaries and overview (clinical submission documents) and Regulatory response documents (Q&A).

You will act as a primary contact for stakeholders on Clinical Reporting-driven content, drive discussions to ensure decisions align with strategy, and represent Clinical Reporting in relevant project groups.

Key responsibilities

Efficiently manage and deliver on clinical reporting and medical writing deliverables while maintaining high quality standards.
Implement project strategies into documents and review project/study-specific materials as needed.
Engage stakeholders to identify needs, timing and scope of clinical reporting deliverables and ensure alignment with the Clinical Reporting strategy.
Support execution of the Clinical Reporting vision and contribute to process improvements and efficiency initiatives.
Share knowledge, mentor colleagues, and contribute to training activities to build capability across the team.
Apply a quality mindset and maintain up-to-date knowledge of global regulatory requirements and policies relevant to your work.

Your Skills and Qualifications

To be successful in this role, you should have the following qualifications:
Must have PhD, Medical degree or Master’s degree (MSc, M Pharm, Pharm D or equivalent) combined with relevant experience.
Experience: At least 2 years’ experience in regulatory medical writing
Experience across a broad range of scientific writing tasks; experience in the pharmaceutical industry or equivalent is desirable
Able to work independently on well-defined tasks with appropriate guidance, strong analytical skills, persistence, accountability, and ability to manage variable workloads.
Communication: Fluent in written and spoken English with the ability to translate complex scientific data into clear, concise, and engaging content tailored to diverse audiences.
Collaboration & stakeholder management: Good project management skills; skilled at fostering cross-functional collaboration across multidisciplinary teams and maintaining professional, trustworthy communication with integrity.
Additional attributes: Cultural awareness for global collaboration, willingness to seek feedback and continuously improve, and a quality-focused mindset.

Your New Department

The Clinical Reporting unit in GBS has seen a tremendous growth curve and has become an integral part of the Global Clinical Reporting community, since its inception in 2011. The team is a dynamic mix of enthusiastic and qualified skilled Medical Writer and, Disclosure Medical Writers with Masters/PhD in life sciences, pharmacology, medicine, etc. The team is full of commitment, passion, skills, and talent with broad knowledge on different therapeutic areas and regulatory requirements for submissions. The team has an average experience of 7 to 8 years in writing and reviewing regulatory documents. We use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials. The department partners closely with cross-functional stakeholders across Medical and Science, Clinical Pharmacology, Biostatistics, Trial Execution, and Regulatory Affairs. The department emphasizes knowledge sharing, innovation, and continuous improvement to support multi-regional clinical studies and ensure cohesive, high-quality deliverables.

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination, and a constant curiosity. For over 100 years, this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect, and a willingness to go beyond what we know delivers extraordinary results.

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

More Information

To submit your application, please upload your CV online (click on Apply and follow the instructions).You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. Internal candidates must inform their respective reporting Managers before applying for the role.

Deadline

19th June 2026

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Apply Now

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medical writer jobs in bangalore city bengaluru karnataka

Medical Writer

2500_ Medical Writer

Medical Writer - Manager

Medical Writer

Regulatory Medical Writer

Sr Safety Medical Writer

Medical Writer - Senior Executive

Lead Medical Writer

1700_SR Medical Writer

Technical Writer

Medical Writer/ Senior Medical Writer

Senior Scientific Writer – Contract

Senior Medical Writer

Medical Communication Writer

Medical Tagging / Writing

Senior Medical Writer

Senior Medical Writer

Associate Director, Medical Writing

Lead Expert - Scientific Writer

Regulatory Analyst - Clinical Affairs

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