
Clinical Data Specialist
2 weeks ago
Job Title: Senior Clinical Trial Transparency Associate
About the RoleYou will join our clinical research organization as a Senior Clinical Trial Transparency Associate, overseeing and coordinating redaction activities across multiple delivery units.
- Candidates should have experience in redaction and protection of personal information in the scientific field (pharma, CRO, or other).
- Previous experience in clinical document management or scientific writing support is required.
- A basic understanding of clinical trial disclosure requirements and proficiency in electronic document management systems are essential.
We are seeking an experienced professional with knowledge of health agency regulations and guidelines related to data transparency.
This role involves applying data transparency standards, requirements, processes, and policies to ensure compliance with regulatory bodies.
ResponsibilitiesYour key responsibilities will include:
- Coordinating operational aspects of transparency activities, such as collecting content for redaction/anonymization from identified points of contact (PoCs), partnering with anonymization providers, issuing and releasing anonymized content.
- Ensuring data transparency deliverables are tracked and published using appropriate systems/tools.
- Providing document management services, including document repository management, indexing, and archiving according to quality standards.
Our competitive benefits package includes annual leave entitlements, health insurance, retirement planning, an Employee Assistance Programme, life assurance, and flexible country-specific optional benefits.
We value inclusion and belonging in our culture and provide an inclusive and accessible environment for all candidates.
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