Clinical Trial Operations & Regulatory Affairs Specialist

Meditrial is looking for a full-time Clinical Affairs professional in New York to manage project-level operations including trial timelines and budgets. Candidates should possess a Bachelor's degree in Life Sciences and previous experience in a pharmaceutical, CRO, or medical device company. Proficiency in GCP/CFR/ICH guidelines is required. The position involves leading trial start-up processes and ensuring high-quality deliverables. Strong communication and organizational skills are essential for success in this dynamic environment.
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