Pharmaceutical Industry Transparency Expert
2 weeks ago
Our Commitment to Transparency
Genmab is committed to promoting transparency in clinical trial research, recognizing the scientific and ethical value of sharing clinical trial information in an unbiased and timely manner.
As a Sr. Associate/Manager in the CTD&T team, you will play a crucial role in ensuring the high-quality disclosure of clinical trial information and implementing new transparency requirements.
Key Responsibilities:
- Execute global and national clinical trial disclosure requirements across Genmab's entire portfolio.
- Support trial teams in developing and maintaining timelines for protocol registration and results disclosure.
- Author or oversee the development of plain language results summaries.
- Develop and update SOPs, templates, and oversee applicable system implementations.
- Train internal staff and vendors on disclosure processes to ensure regulatory compliance.
- Monitor the external landscape to ensure Genmab's adherence to relevant industry guidelines.
About You
- You are passionate about improving patient lives through innovative cancer treatment.
- You bring expertise and rigor to all your work.
- You are a generous collaborator who can work in diverse teams.
- You are determined to do and be your best and take pride in enabling great work from others.
- You are not afraid to grapple with the unknown and innovate.
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