Clinical Trial Posting Associate

Major Responsibilities

• Provide up to date and consistent Clinical Trial Posting data on all required company owned and public websites
• Contribute to continuous monitoring for changing and new Clinical Trial Posting requirements to keep the Global Development Management up to date and to adjust and update the global strategy, and internal rules and processes accordingly
• Formal quality control of publicly disclosed clinical trial information according to the QA process established
• Collection of the necessary data for public disclosure of clinical trial information within BHC: design forms/templates, request information, track responses, disclose information

Education, Know How and Experience

• Medical education, graduate in Natural Science or equivalent professional experience
• Professional experience as CRA, Study Manager
• 1-2 year working experience as ‘Junior Clinical Trial Posting Associate’, or equivalent Webposting working experience
• Experience in clinical development with significant experience related to clinical trials
• Good understanding of ICH/GCP regulations
• Understanding of global legislations, regulations and guidelines