Eli Lilly Hiring for Regulatory Writer
| Job Role | Regulatory Writer |
|---|---|
| Company | Eli Lilly (ICON) |
| Location | Bengaluru |
| Experience | 1 to 2 Years |
| Salary | 5.10 LPA |
| Education | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences |
| Skills Needed | Regulatory Writing, Project Management, Communication, Time Management |
| Key Responsibilities | Content Strategy, Document Preparation, Stakeholder Management, Knowledge Sharing |
Step into the Role of Regulatory Writer at Eli Lilly
Are you passionate about scientific writing and looking to contribute to life-changing medicines? Eli Lilly is seeking a Regulatory Writer to join our team in Bengaluru. In this role, you’ll collaborate with cross-functional teams, transforming scientific data into documents aimed at regulatory agencies. Your work will be integral to supporting clinical development and product registration efforts. Eli Lilly Hiring for Regulatory Writer
Why Work with Eli Lilly?
Eli Lilly is dedicated to advancing scientific knowledge while improving patients’ lives through innovative medicines. As a Regulatory Writer, you will have the opportunity to work in a stimulating environment, writing documents that impact drug development and the regulatory approval process.
We value work/life balance, time management, and flexibility, ensuring that our team members can thrive both professionally and personally. You’ll gain hands-on experience in various therapeutic areas and have the chance to work alongside industry experts while making a meaningful impact on global healthcare. Eli Lilly Hiring for Regulatory Writer
Your Key Responsibilities
As a Regulatory Writer, your main responsibility is to ensure that the scientific and regulatory documentation you create meets the highest standards. You will manage the entire document development lifecycle, from gathering data to finalizing submissions, ensuring regulatory compliance and scientific accuracy. Eli Lilly Hiring for Regulatory Writer
1. Content Strategy and Execution
- Document Preparation and Management: You’ll collect and evaluate scientific data from various sources to develop a content strategy. Your role includes writing, editing, and reviewing regulatory documents such as clinical trial reports and documents supporting product registration.
- Team Collaboration: Initiate and lead meetings to ensure alignment within multidisciplinary teams, making sure that everyone is on the same page for successful document development.
- Scientific Accuracy: You’ll be responsible for building science-based rationales that support complex documents. Presenting clear, concise, and accurate data is key to ensuring the success of regulatory submissions.
- Document Consistency: Ensure all documents are consistent in terms of format, content, and data presentation. You will also coordinate expert reviews and incorporate their feedback to finalize high-quality documents.
Eli Lilly Hiring for Regulatory Writer
2. Project and Stakeholder Management
- Effective Project Leadership: Lead the document writing process using project management skills. Ensure high-quality deliverables while sticking to agreed timelines. You’ll also anticipate risks and work proactively to mitigate them.
- Communication with Stakeholders: Regularly update team members and stakeholders on the status of your projects. This ensures alignment across the board and highlights any potential roadblocks.
Eli Lilly Hiring for Regulatory Writer
3. Knowledge and Skills Development
- Therapeutic Knowledge: Maintain a strong understanding of the therapeutic areas, including diseases and treatments, to ensure that your writing is both technically accurate and compelling. Stay updated on new regulatory guidelines and best practices in scientific communication.
- Adaptability: You’ll handle different types of documents across various therapeutic areas. This requires flexibility and a willingness to expand your knowledge base constantly.
Eli Lilly Hiring for Regulatory Writer
4. Knowledge Sharing and Mentorship
- Coaching and Mentorship: Share your expertise with peers and colleagues by providing guidance on best practices. Help others grow their knowledge of regulatory writing and document management.
- Contribute to Process Improvements: You’ll have the opportunity to contribute to process improvements by sharing best practices and using your knowledge of document management systems to streamline workflows.
Skills You Need to Succeed
1. Scientific and Regulatory Writing Expertise
Having a strong foundation in technical and regulatory writing is a must for this role. You should have experience drafting and editing scientific documents intended for regulatory submission, ensuring they meet all guidelines and are scientifically sound. Eli Lilly Hiring for Regulatory Writer
2. Project Management and Time Management Skills
As a Regulatory Writer, you’ll be juggling multiple documents and timelines. Your ability to effectively manage time and lead projects from start to finish will be critical to your success. Ensuring that projects are delivered on time and to a high standard is essential.
3. Strong Communication and Interpersonal Skills
This role requires excellent communication skills, both written and verbal. You’ll need to be able to explain complex scientific concepts clearly and work closely with cross-functional teams. Building strong relationships with internal and external stakeholders is key to navigating the regulatory landscape. Eli Lilly Hiring for Regulatory Writer
4. Knowledge of Therapeutic Areas
Staying up-to-date with various therapeutic areas and regulatory guidelines is crucial. Your understanding of disease states, treatments, and the clinical development lifecycle will enhance your ability to write accurate and relevant regulatory documents. Eli Lilly Hiring for Regulatory Writer
5. High-Level Technical Skills
Proficiency in using word processing tools, spreadsheets, and document management systems is essential. You should also have a good grasp of tools used to generate tables, graphs, and scientific illustrations.
Preferred Qualifications
While a Bachelor’s degree is the minimum requirement, we highly value applicants with a Graduate degree in life sciences or those with a formal research background. Experience in clinical development, clinical trial processes, or other regulatory activities is highly preferred. Mastery of verbal and written English, especially in medical or scientific writing, will set you apart from other candidates.
Apply Now to Make an Impact
If you’re ready to take on a new challenge and grow your career in regulatory writing, apply now for the Regulatory Writer position at Eli Lilly. This role offers the opportunity to work with some of the best minds in the industry while contributing to life-changing innovations.
Your journey towards making a meaningful impact in global healthcare starts here. Don’t miss the chance to be part of a team that’s driving forward the future of medicine. Apply online and take your first step toward an exciting career at Eli Lilly!