Clinical Disclosure Specialist
7 days ago
About the Role
">We are seeking an experienced Clinical Disclosure Specialist to join our team in Copenhagen or Utrecht. As a key member of our Clinical Trial Disclosure & Transparency team, you will be responsible for executing global and national clinical trial disclosure requirements across Genmab's entire portfolio.
">Your Key Responsibilities
">- You will manage, track, and oversee public disclosure of clinical trial protocols, results, and document redaction.
- You will develop and maintain timelines for protocol registration and results disclosure on platforms such as ClinicalTrials.gov and EU CTIS.
- You will author or oversee the development of plain language results summaries.
- You will develop and update SOPs, templates, and oversee applicable system implementations.
- You will train internal staff and vendors on disclosure processes to ensure regulatory compliance.
- You will monitor the external landscape to ensure Genmab's adherence to relevant industry guidelines.
- You will manage unsolicited requests via email.
About You
">- You have previous experience with clinical trial disclosure.
- You hold a Bachelor's degree minimum.
- You have 1-3+ years of pharmaceutical industry experience with a good understanding of clinical development.
- You possess excellent written and verbal communication skills.
What We Offer
">Genmab is committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. We are an agile working environment that offers flexibility and work-life balance. Our offices are designed as open, community-based spaces that work to connect employees while being immersed in our state-of-the-art laboratories.
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