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About the job Provide administrative and regulatory assistance to the Regulatory Affairs Study Start-up (RASSU) Department. Assist in compilation and revision of Regulatory Affairs (RA) documents required for clinical trials submissions. What Youll Do Assist in
About the job: Responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets and quality standards are being achieved. What Youll Do: Support Clinical Project Manager / Director in completing clinical project