Looking for pharma jobs in India? ICON plc is hiring a Medical Writer I in Bangalore. Explore this exciting pharmaceutical career opportunity in clinical research and medical writing.
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About the Company
ICON plc is a globally recognized healthcare intelligence and clinical research organization that supports the development of innovative medicines and healthcare solutions worldwide.
With a strong presence across multiple countries, ICON partners with pharmaceutical, biotechnology, and medical device companies to accelerate clinical development and regulatory approvals.
Known for its commitment to scientific excellence, regulatory compliance, and innovation, ICON provides world-class clinical research services that help improve patient outcomes.
The company fosters a diverse and inclusive workplace while offering employees exceptional opportunities for professional growth and global exposure.
Job Details
- Company Name: ICON plc
- Position: Medical Writer I
- Qualification: Bachelor’s Degree in Life Sciences, Pharmacy, Medicine, or related field
- Location: Bangalore (Bengaluru), India
- Work Type: Hybrid / Office-Based
- Job Reference: JR153060
- Department: Medical Writing
- Business Unit: ICON Full Service & Corporate Support
Job Description
ICON is expanding its Medical Writing team and seeking talented professionals interested in clinical research, scientific communication, and regulatory documentation.
This role offers an excellent opportunity to contribute to clinical development programs while working alongside global healthcare experts.
Medical Writer I
- Department: Medical Writing
- Market: Clinical Research & Healthcare Intelligence
- Role: Medical Writer I
- Location: Bangalore, India
- Work Type: Hybrid / Office-Based
- Education/Qualification: Bachelor’s Degree in Life Sciences, Pharmacy, Medicine, or related discipline
Skills & Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related field
- Strong interest in clinical research and drug development
- Excellent written and verbal communication skills
- Ability to simplify complex scientific information
- Strong attention to detail
- Effective organizational and time-management skills
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Familiarity with document management systems
- Knowledge of reference management software
- Understanding of clinical trial documentation
- Ability to work in cross-functional teams
- Adaptability in a fast-paced environment
- Self-motivated with a learning mindset
- Knowledge of regulatory requirements and SOPs
Key Responsibilities
- Prepare clinical study reports and protocols
- Draft investigator brochures and patient narratives
- Support regulatory submission documentation
- Conduct scientific literature reviews
- Analyze and interpret clinical trial data
- Assist manuscript and abstract preparation
- Review clinical data for accuracy
- Ensure compliance with study protocols
- Participate in project meetings and discussions
- Collaborate with cross-functional teams
- Support client interactions and deliverables
- Monitor industry and regulatory updates
Benefits & Perks
- Competitive salary package
- Comprehensive health insurance options
- Retirement and savings benefits
- Flexible employee benefit programs
- Global Employee Assistance Programme
- Life assurance coverage
- Learning and development opportunities
- International project exposure
- Inclusive and collaborative workplace
- Career advancement opportunities
- Strong work-life balance initiatives
- Access to global clinical research expertise
How to Apply
Interested candidates can apply directly through the official ICON Careers Portal.
Career Page:
https://careers.iconplc.com
Job Reference:
JR153060
Applicants are encouraged to submit their applications as early as possible. Even if you do not meet every listed requirement, ICON encourages qualified professionals to apply.
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Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Icon career page.
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Apply today and take the next step in your clinical research and medical writing career with ICON plc.
Why You Should Join ICON plc
ICON offers a unique opportunity to work with one of the world’s leading clinical research organizations. Employees benefit from a culture focused on innovation, collaboration, diversity, and professional growth.
Working at ICON means contributing to groundbreaking healthcare solutions while developing valuable expertise in regulatory writing, clinical research, and scientific communication.
The organization invests heavily in employee development and recognizes talent through meaningful career progression opportunities.
FAQs
Who is eligible to apply for the Medical Writer I position?
Candidates with a Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or a related discipline are eligible to apply.
Is prior medical writing experience mandatory?
The role welcomes candidates with relevant medical writing knowledge and a strong interest in clinical research and scientific communication.
Is this a remote position?
The role is hybrid and office-based in Bangalore, offering a combination of workplace and flexible working arrangements.
What career growth opportunities are available?
Employees gain exposure to global clinical research projects, professional development programs, and long-term advancement opportunities within ICON’s international network.
