Clinical Supplies Program Manager III Job in Gwynedd, Pennsylvania Us

·        5-10 years in clinical research or industry (including Central Labs)

·        Background in biomarker research

·        Background in data analysis/programming (Access database/SAS)-working with Statisticians/Clinical Programmers

·        Strong working knowledge of personal computers in order to assist with clinical data entry and summarization for tracking purposes

·        Strong understanding of the clinical trial processes

·        Hands-on experience working with Central Laboratories, CROs and biorepository specimen management

·        Good oral and written communication skills (includes internal reports, manuscripts, oral presentations and interpersonal skills)

·        Ability to interact and communicate with external companies for both planning and operational execution of a day to day activities

·        Ability to multi-task and prioritize efforts effectively

·        Ability to summarize info/data in a concise, easy to understand manners

·        Team player and able to work in a dynamic setting Dedicated with attention to high quality results