Regulatory Compliance Specialist

6 days ago


Hong Kong, Central and Western District, Hong Kong SAR China myGwork - LGBTQ+ Business Community Full time
Key Responsibilities
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  • Data Verification: Conduct thorough comparisons of Case Report Forms against source documents, verify Informed Consent Forms, and review regulatory documents.
  • Communication: Ensure clear written communication to clinical sites and project team members through monitoring reports, follow-up letters, and study memos.
  • Training: Ensure site personnel are appropriately trained and prepared to conduct clinical studies in accordance with protocol and regulations.
  • Site Compliance: Identify and address non-compliance issues, clearly communicate, document, and escalate as required.

We're looking for a motivated individual with strong analytical skills and attention to detail to join our team as a Regulatory Compliance Specialist - Clinical Trials.



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