At a Glance
- Tasks: Maintain and develop clinical documentation frameworks while ensuring compliance with FDA/ISO/EU MDR standards.
- Company: Join CyDen, a forward-thinking company dedicated to clinical excellence.
- Benefits: Gain valuable experience in a dynamic environment with potential for future opportunities.
- Other info: 5-month contract with a chance to enhance your professional skills.
- Why this job: Make a real impact on clinical operations and collaborate with diverse teams.
- Qualifications: Detail-oriented with experience in clinical documentation and regulatory standards.
The predicted salary is between 28350 - 34650 £ per year.
CyDen is seeking a detail-oriented Clinical Documentation Specialist to maintain and develop the documentation framework for clinical operations. You will define templates, WIs and SOPs at sponsor and site levels, align with evolving FDA/ISO/EU MDR standards, and ensure strict version control and archival procedures.
You will collaborate with medical writers, statisticians, CRA/CTA teams and internal stakeholders to reflect best practices, maintain CRF templates, and support UAT and EDC.
Clinical Documentation Lead - 5-Month Contract in Swansea employer: CyDen
CyDen is an exceptional employer located in Swansea, offering a dynamic work environment that fosters collaboration and innovation in clinical research. With a strong commitment to employee development, we provide ample opportunities for growth and advancement, alongside a supportive culture that values diversity and inclusion. Our focus on maintaining high standards of compliance and data integrity ensures that our team members are engaged in meaningful work that contributes to the advancement of healthcare.
