Lead the clinical protocol development process in collaboration with the Clinical Program Leader. Will be the responsible author for clinical protocols, amendments and related documents; contribute to the medical/scientific input given for the development of trial-related documents and processes which reside in other line functions.

Qualifications:

• Advanced degree or equivalent education/degree in life science/healthcare strongly recommended. PhD preferred.
• 6 years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or CRO
• Knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
• Advanced knowledge of oncology and/or hematology, OR experience in early clinical development is preferred

Candidates must live local and be a US Citizen or Green Card Holder

Email resume to: jobs@cwsciences.com
Commonwealth Sciences is a professional recruiting firm specializing in science, engineering and green technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

Commonwealth Sciences, Inc.
www.cwsciences.com