Project Manager

Medpace, Inc.

Determine study objectives, strategy, scope, and schedule to meet the goals and timelines of the clinical study sponsor; Direct daily activities for the clinical study associates and other team members; Monitor and drive the progress of the clinical study, including identifying potential issues or challenges and developing appropriate solutions; Forecast and budget for the clinical study; and Develop relevant study documents such as Clinical Investigation Plans, Case Report Forms, Data Management Plans, and Monitoring Plans. Qualifications: Bachelor’s degree in life sciences or a related field; At least 5 years of clinical study experience, including prior experience with medical devices and IDE trials; Previous knowledge of GCP for medical device trials, 21 CFR 812 (other sections, depending on role); Outstanding oral and written communication skills; Ability to interact with medical personnel and attend medical procedures; Strong customer service focus and project management skills; High attention to detail and quality standard; and Proficient in Microsoft Office applications. To apply for this position, please send your resume to hr@medpace.com Medpace, Inc. - 30+ days ago - save job - block » Apply Now Indeed will send your application to hr@medpace.com. Please review all application instructions before applying.

Posted 30+ days ago

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