Clinical Research Scientist Resume

Clinical Research Scientist
Clinical Development Strategy ▪ Risk Management ▪ Program Delivery 
Company, Town, XX , Date – Date
Senior Clinical Research Scientist
• Manage the delivery of clinical study protocols, clinical study reports, study agreements, applications and other study documentation such as newsletters and study presentations.
• Lead overall activities and optimize the performance of the study team.
• Monitor study progress such as patient recruitment and protocol compliance.
• Study data listings and tables review, including scientific content and data validation.
• Track and manage studies to agreed timeline, budget and resource, highlighting significant variances to the EML and study team.
• Train internal and external study personnel in study specific procedures.
• Develop detailed study outlines and ensure medical and scientific input in study reports.
• Forecast timelines, budget, materials and resource for a defined component of the CDP.
• Interpret data arising from studies and assess potential consequences for development program.
• Communicate findings to sub-team, clinical development team and pharmacokineticist.
• Assist in non-project work and the development of clinical R&D procedures.
• Provide scientific input to the development of contingencies, where the emerging data require changes to the program and individual studies.
• Implement the amended program of work in accordance with a revised Clinical Development Plan Provision of scientific input into program design.
• Recommend choice of study placement and participate in negotiations with liaison.
University, Town, XX 
Ph.D., Chemistry

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