Description
Director of Clinical Research: OncologyA leading New Jersey based Pharmaceutical company is in search of a highly specialized individual contributor to lead their Oncology program.
As study director you will be leading and providing oversight of global pivotal trials to support the global program leader. This position will have significant input into planned regulatory submissions and future development plans at a strategic level.
As the key individual contributor and functional manager you will be expected to have the in-depth therapeutic knowledge (Oncology) and to be seen as the operational expert on subjects within clinical development, and research.
Accountabilities
Lead and execute key business objectives and projects within the clinical research department
Develop, modify and execute company policies that affect immediate operations that hold effect company wide
Be a core part of innovation teams working on complex clinical research and development problems including analysis of situations, data reviews and evaluations of diverse external factors effecting clinical research.
Process improvement across workloads and processes
Exercise judgment and direction within broadly defined practices and policies, selecting methods and techniques across clinical research
Influence and advice cross functionally
Reporting to the group head you will be supervising and involved with the development of teams in a project setting
Responsibilities
Direct and implement clinical research plans and programs establishing design principals
Direct and integrate CDP and DDP
Lead and development of protocols and to meet CDP objectives
Serve as he study director who drives the study from protocol concept to final report including the interpretation of clinical data.
Serve as Medical monitor and implement strategies to define clinical program issues.
To find out more about Real please visit www.realstaffing.com