Clinical Project Manager position with a biopharmaceutical company in Houston.  This is a full-time, permanent position in the company's headquarters in Houston.

Responsibilities:
•Manage clinical monitoring activities to ensure timely completion and monitoring of CRFs, accurate safety reporting and maintenance of clinical trial files
•Assist in the design, development and implementation of protocols, CRFs and study supporting documents
•Responsible for site recruitment, start-up activities, facilitating enrollment, and final study reports
•Help select the clinical data management group, manage the project and relationship, and ensure timeliness and accuracy of data entry and analysis
•20-30% travel 

Requirements:
•Bachelor’s degree in the sciences
•2+ years in clinical trials project management
•3+ years of clinical trial monitoring experience
•Knowledgeable of ICH/GCP and federal regulations
•Experience with MS Excel, Word, and Power Point
•Oncology experience is strongly preferred