Not specified; competitive within country; benefit...
Office-based
Study start-up experience
Regulatory document submission
Ich-gcp compliance knowledge
ICON Clinical Research is seeking a Senior Site Specialist based in China to lead the initiation of clinical trials while ensuring compliance with regulatory requirements. The ideal candidate will have a background in clinical research, strong organizational skills, and a commitment to fostering an inclusive environment
Job Summary
The role involves leading the initiation of clinical trials while ensuring strict compliance with regulatory requirements.
Candidates will coordinate with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
ICON offers a competitive salary along with diverse benefits including health insurance, retirement planning, and global employee assistance programs.
Matching Summary
Match Score: 85
ICON Clinical Research is seeking a Senior Site Specialist based in China to lead the initiation of clinical trials while ensuring compliance with regulatory requirements. The ideal candidate will have a background in clinical research, strong organizational skills, and a commitment to fostering an inclusive environment.
Salary
Not specified; Competitive within country; Benefits include annual leave, health insurance, and retirement planning
Skills & Requirements
Must-have
Study start-up experience
Regulatory document submission
ICH-GCP compliance knowledge
Stakeholder liaison skills
Cross-functional collaboration
Nice-to-have
Process improvement initiatives
Strong organizational skills
Inclusive environment values
Project management abilities
Key Requirements
Bachelor's degree in life sciences or related field
Minimum 4 years of experience in clinical research or regulatory affairs
Specific experience in study start-up activities
Understanding of local regulatory requirements in China