Eli Lilly and Company Hiring Freshers | Regulatory GSC Scientific Communications Associate – Bangalore
- Eli Lilly and Company Hiring Freshers | Regulatory GSC Scientific Communications Associate
- About Eli Lilly and Company
- Job Overview
- Job Details
- Job Title:
- Location:
- Employment Type:
- Job Category:
- Qualifications:
- Experience Required:
- Key Responsibilities:
- How to Apply?
Eli Lilly and Company Hiring Freshers | Regulatory GSC Scientific Communications Associate
About Eli Lilly and Company
Eli Lilly and Company is a leading global healthcare organization headquartered in Indianapolis, Indiana. With a commitment to innovation and improving lives, Lilly focuses on discovering life-changing medicines and delivering quality healthcare solutions worldwide. The company fosters an inclusive work environment that values diversity, innovation, and integrity.
Job Overview
Eli Lilly and Company is currently hiring freshers for the Regulatory GSC Scientific Communications Associate role in Bangalore, Karnataka, India. This is an excellent opportunity for individuals with a background in science, healthcare, or communications who are passionate about scientific writing and regulatory documentation.
Job Details
Job Title:
Regulatory GSC Scientific Communications Associate
Location:
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📱 Get More DetailsBangalore, Karnataka, India
Employment Type:
Full-time | Regular
Job Category:
Research & Development
Qualifications:
- Bachelor’s degree in a scientific, health, communications, or technology-related field.
- Strong communication and interpersonal skills.
- Demonstrated experience in technical or regulatory scientific writing.
- Successful completion of a writing exercise (mandatory as part of the candidate evaluation process).
Experience Required:
- Freshers and experienced candidates with up to 2 years of experience in regulatory writing are encouraged to apply.
Key Responsibilities:
1. Scientific Communications & Document Development
- Develop and manage regulatory documents such as protocols, amendments, informed consent forms, and clinical study reports.
- Collect, evaluate, and synthesize scientific data to create clear and compelling regulatory documents.
- Ensure accuracy, consistency, and compliance with industry standards and regulatory guidelines.
- Coordinate internal and external expert reviews and manage document updates based on feedback.
2. Project & Stakeholder Management
- Lead the writing process, ensuring timely delivery of high-quality documents.
- Establish and communicate project timelines to stakeholders.
- Identify potential risks and develop mitigation strategies.
3. Knowledge Development & Sharing
- Maintain up-to-date knowledge of therapeutic areas, regulatory guidelines, and publication standards.
- Participate in scientific and clinical planning discussions.
- Provide coaching and mentorship to team members, sharing best practices.
How to Apply?
Interested candidates can apply through the official Eli Lilly careers portal:
👉 Apply Here
To apply for this job please visit careers.lilly.com.