Clinical Trials Transparency Specialist
22 hours ago
We are seeking a skilled Clinical Trial Registry and Transparency Associate to lead the development and preparation of documents for public disclosures, ensuring global transparency regulations and requirements are followed.
This exciting opportunity allows you to develop and enhance your knowledge of transparency regulations, guidelines, and industry best practices while collaborating with cross-functional teams across multiple geographies and phases of drug development.
The successful candidate will be responsible for content strategy and execution, project management, knowledge and skills development, and knowledge sharing. To succeed in this role, you will require a strong understanding of transparency regulations, excellent communication and project management skills, as well as the ability to work effectively in a team environment.
Key Responsibilities:- Content Strategy and Execution: Document Preparation, Development and Finalization/Document Management
- Project and Stakeholder Management: Lead the content creation and/or redaction process and apply effective project management skills to ensure timely completion of high-quality transparency deliverables.
- Knowledge and Skills Development: Maintain and enhance knowledge of transparency regulations and guidelines.
- Knowledge Sharing: Provide coaching to others by sharing technical information, giving guidance, answering questions.
If you are a motivated and detail-oriented individual with a passion for scientific communications, we encourage you to consider this opportunity.
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