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1700 sr Medical Writer
1 month ago
**Position Description**:
The Senior Medical Writer Commercial Learning Services (CLS) is responsible for
the development of medical content including but not limited to creating/updating wireframes,
building reference packages, creating/updating learning content for product trainings for
assigned areas at both Global and affiliate level. The Medical Writer will anticipate and adjust for
problems and roadblocks, interface with partners at Indianapolis and
LCCI and integrate new business processes where necessary. Using strong adult learning
principles, Medical Writer ensures quality design, development, and delivery of training
development projects. This role will interact with a wide variety of people both in LCCI and the
US, at varying levels of the business. The role will report to Manager-CLS at LCCI.
**Key Objectives/Deliverables**:
Medical Writing (Content Development)
- Partners with learning consultants and business partners to effectively gather and
evaluate source content from multiple sources.
- Plans (including organizing/preparing outlines), write (including first-draft authoring),
edit, review, and coordinate the creation of medical learning content (storyboard)
- Ensures that key content, scientific concepts, elements from internal guidance and
resource documents are included appropriately in all learning content, and that all
documents are well written, usable/executable, and compliant with policies and
procedures.
- Ensures proper documentation of needed references and attribution of source material.
- Ensures and coordinates quality checks for accuracy, collate reviewer’s comments,
adjust content of training as required based on internal/external input, and prepare final
version.
- Drives quality standards through review of project documents, design, deliverables, final
learning content and evaluation data.
Project and Stakeholder management
completion of high-quality regulatory documents.
- Effectively manage multiple projects and exhibit flexibility in moving across therapeutic
areas, and products, depending on project assignment.
- Builds, communicates, and manages credible project timelines.
- Influences or negotiates changes of timelines and content with other team members.
- Anticipates and mitigates risks to delivery.
- Anticipates and resolves project/program issues, escalating as appropriate.
Knowledge Sharing and Development
- Maintains and enhances therapeutic area knowledge including disease state and
compound(s) for assigned project(s).
- Maintains and enhances the medial writing skills to align with the audience needs and
with the changes in technology and platforms.
- Provides coaching to others by sharing technical information, giving guidance, answering
questions.
- Networks with others (including other functions and regions) to identify and share best
practices.
- Contributes to process improvements, suggesting opportunities where appropriate.
**Basic Requirements**:
- Demonstrated experience in technical scientific or medical writing.
- Demonstrated excellence with program/project management and time management
skills.
- Demonstrated ability to establish strong business relationships.
- Ability to work independently and in a team environment.
- Demonstrated ability in conflict resolution, judgment and managing complexity.
- Ability to prioritize work and balance multiple projects simultaneously.
- Strong work ethic, personal motivation, and team player who is dynamic and result
oriented
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