At a Glance
- Tasks: Lead global clinical trial disclosures and ensure compliance with regulations.
- Company: Join a leading biopharmaceutical company focused on innovation and transparency.
- Benefits: Attractive salary, comprehensive health benefits, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on collaboration and excellence.
- Why this job: Make a significant impact in clinical research and contribute to global health.
- Qualifications: Experience in clinical trial processes and strong strategic oversight skills.
The predicted salary is between 63000 - 77000 £ per year.
The Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational). This role guides global strategy, drives process excellence, and oversees the delivery of clinical trial disclosure activities including registration, results disclosure and layperson summaries while providing support for transparency activities including anonymization and redaction of commercially confidential information (CCI) as required for business continuity and operational needs. All activities and deliverables must be conducted in alignment with international regulations, CSL policies, industry standards and transparency requirements.
Key Responsibilities
- Strategic Oversight
Associate Director T & D employer: CSL
As an Associate Director in Procurement Enablement at CSL, you will be part of a forward-thinking organisation that prioritises sustainability and governance while fostering a culture of continuous improvement and talent development. With a commitment to employee growth through the Global Procurement Academy and a collaborative work environment, CSL offers a unique opportunity to influence procurement practices on a global scale, making it an excellent employer for those seeking meaningful and impactful careers.
