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Eli Lilly and Company

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3.9

based on 393 Reviews

63 Eli Lilly and Company Jobs

LCCI Editor - Medical Affairs

Eli Lilly and Company

3.9

based on 393 Reviews

2-4 years

Bangalore / Bengaluru

1 vacancy

LCCI Editor - Medical Affairs

Eli Lilly and Company

posted 2mon ago

Job Role Insights

Flexible timing

Key skills for the job

Project Management Analytical Chemistry Publishing New Product Development Medical Affairs Oncology

+ 2 more

Job Description

Organization Background

Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals (HCPs), payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly.

As HCPs are deluged with data and are making choices in an increasingly complex and stressed health system, Lilly Medical Affairs (MA) can provide clear, credible answers that will set Lilly apart from its competitors. MA mission is to make Lilly the preferred pharmaceutical partner in the healthcare community globally by leveraging its medical expertise to drive patient-centric answers and solutions. MA brings deep medical expertise to HCPs and payers and focuses on answering HCP questions with customized clinical and real-world evidence that can make the difference on if and how they use Lilly products. Additionally, MA brings clinical insights from customers back to Lilly to inform new product development and lifecycle planning. MA also supports patients with educational tools to help them manage their illness and with assistance to access our medicines for those facing tough financial situations.

Position Description

The purpose of the Copyeditor s role in Medical Affair Quality is to review and copyedit U.S. medical (non-promotional) and promotional materials across different therapeutic areas and brands to ensure they adhere to Customer Information Quality (CIQ) and/or Medical Content Approval (MCA) requirements and corresponding process requirements.

The Copyeditor will leverage different content, project, and quality management tools to increase speed and efficiency in the review and approval of promotional and medical (non-promotional) materials.

Primary Responsibilities:

This job description intends to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.

Copyedit of promotional and medical (non-promotional) materials

Thorough understanding of Lilly s quality requirements and processes (ie, CIQ and MCA requirements) and applying these guidelines during the review process
Collaborate with cross-functional teams such as Marketing, Medical teams, etc. during the review, approval, and management of content, including attending review meetings as and when required
Validate content is aligned to CIQ and MCA requirements, ensuring consistency across related materials
Review materials following provided style guides, templates, and against a checklist
General knowledge of scientific literature search and retrieval
Proofread or copyedit assigned deliverables to meet quality standards, independently
Review/proofread the usage of language, grammar, style, spelling, grammar, and consistency to ensure readability of the document
Identify and fix flaws in logic and flow
Review the reference list for compliance to AMA Manual of Style/brand style
Expertise in tools and platforms such as Veeva Vault, project planning software (e.g., Wrike, MS Project), etc.

Ensure quality, speed, value, and compliance throughout the review process

Support and adhere to organizational project management best practices
Responsible and accountable for completing the assigned tasks by:
- Uphold Lilly procedures and processes
- Review and approve materials in a timely manner
- Determine corrective actions to eliminate recurring issues
- Liaising with CIQ/MCA Lead and Operations teams in tracking and managing deviations
Partner effectively with cross-functional colleagues and facilitate shared-learning forums to establish best practices and identify challenges across teams
Adhere to best practices based on Lilly internal standards
Identify ways to continuously improve processes

Minimum Qualification Requirements:

2-4 years of experience as an editor, copyeditor, or proofreader of promotional and medical (non-promotional) content for publishing, marketing, communications, or advertising agencies, or pharmaceutical industry.
Familiarity with various style guides including AMA Manual of Style/Chicago Manual of Style
Must have good understanding of scientific/medical terminologies
Demonstrated initiative and ability to influence, collaborate, and work on cross-functional teams and ability to make decisions within scope of responsibility
Demonstrated ability to prioritize and handle multiple concurrent tasks with strong attention to detail, critical thinking, and analytical ability
Excellent written and verbal communication skills
Ability to work well independently or as part of a team, within and across culturally and geographically diverse environments

Additional Preferences:

In-depth familiarity with the US CIQ/MCA framework, procedures, processes, and tools like Veeva Vault, project planning software (e.g., Wrike, MS Project), etc.
Experience reviewing/writing Medical Affairs communications deliverables (slide decks, patient, or HCP materials, etc.)
Knowledge and experience specific to clinical pharmacology, therapeutic areas such as neuroscience, oncology, cardiovascular, immunology or endocrinology, or other medical and scientific fields

Educational Requirements: