Study Start Up Associate - Ivdr Experience Required
ICON
United Kingdom
Not specified; not specified; competitive within c...
Fully remote
Ivdr experience required
Uk based remote work
Regulatory document preparation
ICON is seeking a Study Start Up Associate with IVDR experience to support clinical research operations. This fully remote position requires strong organizational skills and the ability to manage multiple tasks while collaborating with stakeholders to ensure regulatory compliance
Job Summary
The role involves delivering site start-up and activation work to a high standard while working closely with stakeholders.
Responsibilities include assisting in the preparation and submission of regulatory documents such as clinical trial applications and ethics committee submissions.
ICON offers a competitive salary along with various benefits including health insurance, retirement planning, and a global Employee Assistance Programme.
Matching Summary
Match Score: 85
ICON is seeking a Study Start Up Associate with IVDR experience to support clinical research operations. This fully remote position requires strong organizational skills and the ability to manage multiple tasks while collaborating with stakeholders to ensure regulatory compliance.
Salary
Not specified; Not specified; Competitive within country with range of additional benefits
Skills & Requirements
Must-have
IVDR experience required
UK based remote work
regulatory document preparation
site start-up and activation
Nice-to-have
strong attention to detail
excellent communication skills
ability to collaborate with cross-functional teams
willingness to travel approximately 5%
Key Requirements
Bachelor's degree in life sciences or related field