
Clinical Trials Specialist
4 days ago
We are seeking a dedicated individual to join our team as a Clinical Trial Registry and Transparency Associate.
This role involves working with global healthcare leaders to develop and implement strategies that promote transparency and accountability in clinical trials.
As a member of our team, you will be responsible for leading the development and preparation of documents for public disclosures, ensuring compliance with global regulations and requirements.
You will also build credible project timelines, anticipate and mitigate risks to delivery, and effectively communicate project status to stakeholders.
In addition, you will maintain and enhance your knowledge of transparency regulations and guidelines, therapeutic area knowledge, and plain language/health literacy concepts.
Requirements- Bachelor's degree in a scientific, health, or communications related field or equivalent experience.
- High-level end-user computer skills (Adobe, MS Office applications).
- Mastery of English language skills, written and spoken.
- Develop and execute content strategy to ensure global transparency regulations are followed.
- Build and manage project timelines, identify and mitigate risks, and communicate project status to stakeholders.
- Stay up-to-date on transparency regulations, therapeutic areas, and plain language/health literacy concepts.
- Coach others by sharing technical information and providing guidance.
If you are passionate about promoting transparency and accountability in clinical trials, we encourage you to apply for this exciting opportunity.
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