Sr. Manager responsible for the integrity and execution of clinical trials in biopharmaceutical industry. Collaborating with cross-functional medical and operational teams to ensure high-quality clinical study delivery.
Responsibilities
Accountable for the scientific integrity of the study and the well-being of the patients enrolled in one or more clinical trials
Apply technical and clinical skills to ensure the design of efficient and high-quality clinical trials
Responsible for effective execution of studies and works in close partnership with other clinical and medical colleagues, clinical operations, and other functional lines
Accountable for timely delivery of a quality protocol, clinical execution of clinical trials and supports appropriate interpretation and communication of clinical trial data
Maintains compliance with internal and external standards, proactively mitigates risk and manages emerging clinical issues through timely, diligent clinical data, safety and protocol deviation review
Primary contact with external investigators & the internal study team for questions relating to clinical aspects of the protocol
Requirements
BA/BS or equivalent qualification with 6+ years of experience in biopharmaceutical industry in clinical research and development
MBA or MS equivalent with 5+ years of experience
Advanced Degree with 1+ years of experience
Demonstrated clinical, administrative, and project management capabilities
Excellent verbal and written communication skills in English
Clinical research experience in phase 3/pivotal space highly preferred
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