Hbr Layout Bengaluru Karnataka Clinical research associate Jobs – 73 Open Jobs Today

Associate Regulatory Specialist
Novo Nordisk —Bengaluru, Karnataka
- Doctoral degree
- English
- Master's degree
9h
Senior Medical Writer
Navitas Life Sciences —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Medicine
Senior Medical Safety Advisor
IQVIA —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Front Office and Admin Associate
MS CLINICAL —Bengaluru, Karnataka
- Microsoft Powerpoint
- Microsoft Word
- CRM software
13d
Solutions Design Analyst, Specialty Solutions
Clario —Bengaluru, Karnataka
- Full-time
- Doctoral degree
- B.Sc
- English
Research Associate – International Voice Calling
m360 Research —Bengaluru, Karnataka
- Full-time
- English
- 12th Pass
- Bachelor's degree
Quick apply
1700_Project Statistician
Recruise —Bengaluru, Karnataka
- Full-time
- Doctoral degree
- Master's degree
- Leadership
Quick apply
Manager, Project Delivery - OptymEdge
Emmes Group —Bengaluru, Karnataka
- Full-time
- Microsoft Word
- Management
- Microsoft Office
Business Development Associate
Clini launch Research Institute —Bengaluru, Karnataka
- Up to ₹18,000 a month
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
2d
Recipient Services Trainee - South
Cochlear Ltd —Bengaluru, Karnataka
- Full-time
1700_Associate Director – Statistical Programmer
Recruise —Bengaluru, Karnataka
- Full-time
Quick apply
Business Development Associate (BDA)
Clini launch Research Institute —Bengaluru, Karnataka
- ₹18,000 - ₹20,000 a month
- Full-time
- CRM software
- Microsoft Office
- Master's degree
Quick apply
3d
Technical Lead
Eurofins GSC IT DC —Bengaluru, Karnataka
- Full-time
- Azure
- Computer Science
- Software troubleshooting
Quick apply
Physiologists
Digi Prime Tech Pvt Ltd —Bengaluru Rural District, Karnataka
- ₹80,000 - ₹3,00,000 a month
- Full-time
- B.Sc
- Research
- Master's degree
- Health insurance
- Paid time off
Quick apply
17h
Medical Science Liasion
Novartis —Bengaluru, Karnataka
- Full-time
- Medicine
- Doctoral degree
- English
13h
Data Entry Associate I
Labcorp —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
7h
System Engineer I
Beckman Coulter Diagnostics —Bengaluru, Karnataka
- Full-time
- Computer science
- Engineering
- Analysis skills
- Paid time off
18h

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Pharmacists
Digi Prime Tech Pvt Ltd —Bengaluru Rural District, Karnataka
Candidates should possess strong knowledge of medicines, prescription handling, patient counseling, inventory management, and regulatory compliance.
₹50,000 - ₹1,00,000 a month
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17h
Business Development Associate
Clini launch Research Institute —Bengaluru, Karnataka
Exposure to the clinical research and healthcare education industry. Pay: Up to ₹18,000.00 per month. The ideal candidate will be responsible for generating…
Up to ₹18,000 a month
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2d

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Associate Regulatory Specialist

Novo Nordisk -
Bengaluru, Karnataka

Apply Now

Job details

9 hours ago

Qualifications

Doctoral degree
English
Master's degree
Project management
Bachelor's degree
Research & development
Communication skills

Full job description

Associate Regulatory Specialist

Category: Reg Affairs & Safety Pharmacovigilance

Location: Bangalore, Karnataka, IN

Company: Novo Nordisk Global Business Services (GBS)

Shape regulatory strategies that bring life-changing diabetes therapies to patients in every corner of the world. As an Associate Regulatory Specialist, you'll be the link between science, health authorities and the millions of people who depend on our medicines – with the autonomy to set direction, the expertise to influence outcomes, and the support of a global team behind you.

Your new role

As an Associate Regulatory Specialist in RA Diabetes, you will take ownership of regulatory submissions and interactions across major markets, acting as a subject matter expert within one or several regulatory processes. You'll work independently on most situations while shaping better practice for the team, mentoring junior colleagues and driving the regulatory strategy that supports our diabetes portfolio.

Day-to-day, your responsibilities will span:

Global regulatory submissions: Develop and execute Regulatory Affairs Submission Plans in Vault RIM, prepare and publish regulatory files, and manage MAA/NDA/BLA, CTA/IND, PIP/PSP submissions, renewals, post-approval changes, pharmacovigilance documents (DSUR, PSUR, RMP), and meeting packages worldwide
Health Authority interactions: Plan and conduct engagements with FDA, EMA, PMDA and other authorities – including preparing meeting requests, leading rehearsals and capturing minutes of formal meetings
Core labelling: Establish and maintain the target CCDS/CCDS and European labelling for products in development, link the Target Product Profile to commercial and market access requirements, and support US labelling and Life Cycle Management
RA Process expertise: Identify and develop better practice, driving improvements in regulatory documentation, methods and strategies
RA Due Diligence: Lead regulatory due diligence assessments to inform business decisions
RA Clinical expertise: Chair or contribute to Clinical Project / Clinical cross-functional groups, applying your submission experience across China, Japan, US and EU

Your new department

In Research & Development, you'll be part of a unit that explores bold scientific ideas and advances them into clinical testing. We combine curiosity, AI tools, and human data to develop transformative therapies. Through collaboration and operational excellence, we shape and deliver an innovative pipeline to meet future patient needs.

You will join RA Diabetes in Global Regulatory Affairs Bangalore, reporting to the Associate Director, RA Diabetes. The department works globally with Clinical Operations, Medical & Science, Global Safety, Global Medical Affairs, Global Marketing/Patient Access, Legal, Quality, RA affiliates and health authorities to support product development, approvals and lifecycle management. Together, we focus on high-quality regulatory submissions, continuous process improvement and collaborative cross-functional engagement to bring safe and effective therapies to patients worldwide.

Your skills & qualifications

We're looking for a confident regulatory professional who combines deep technical knowledge with a strategic mindset and the boldness to make risk-based decisions. To succeed in this role, you'll bring:

A PhD, Master's or Bachelor's degree in life sciences, with 7–9+ years of relevant Regulatory Affairs experience – or equivalent knowledge gained through practical experience
Strong expertise across several regulatory affairs disciplines such as regulatory science & requirements (EU, US, China, Japan), Life Cycle Management, label development, Health Authority interactions, device development, regulatory intelligence and therapeutic area knowledge
Submission experience across major markets (China, Japan, US, EU) and a track record of identifying and implementing process improvements
Broader understanding of project management, the R&D value chain, pharmacovigilance, clinical pharmacology, real world evidence, digital health and patient access
Excellent written and spoken English, with strong cross-functional communication skills and the ability to operate effectively in a multicultural environment
An open, accountable and inclusive mindset – goal-oriented, organised, persistent, and able to handle ambiguity, variable workloads and complex information with empathy and a collaborative spirit

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health – one where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job; you're stepping into a defining moment in our history, where your regulatory expertise directly shapes how millions of people living with diabetes access the therapies they need.

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.

Deadline

18 June 2026. Applications are reviewed on an ongoing basis, so please apply as soon as possible.

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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clinical research associate jobs in hbr layout bengaluru karnataka

Associate Regulatory Specialist

Senior Medical Writer

Senior Medical Safety Advisor

Front Office and Admin Associate

Solutions Design Analyst, Specialty Solutions

Research Associate – International Voice Calling

1700_Project Statistician

Manager, Project Delivery - OptymEdge

Business Development Associate

Recipient Services Trainee - South

1700_Associate Director – Statistical Programmer

Business Development Associate (BDA)

Technical Lead

Physiologists

Medical Science Liasion

Data Entry Associate I

System Engineer I

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