Associate Director overseeing global research studies at Summit Therapeutics, enhancing oncology evidence. Driving strategy and collaboration across multiple teams for successful execution.
Responsibilities
Independently oversee all operational aspects of non-sponsored research studies
Deliver comprehensive end-to-end management
Responsible for identifying key data gaps and developing strategies
Develop metrics and dashboards to monitor the progress and impact of data generation initiatives
Foster and maintain strong relationships with external stakeholders
Provide guidance and support for the review and approval of study concepts and protocols
Requirements
Advanced degree (PhD or equivalent) in life sciences or related field highly preferred
Minimum of 7+ years of experience in a relevant role within the pharmaceutical industry required
Familiarity with clinical research terminology required
Experience working in clinical trial management, research management, and/or Medical Affairs research programs
Experience producing and analyzing metrics/reports
Strong clinical/scientific acumen required including the ability to interpret, analyze, organize, and communicate scientific data
Proficient user of standard MS Office suite (e.g., Word, Excel)
Experience with IST management software platforms (e.g. iEnvision ISR platform) and tools and fair market value analysis (e.g. IQVIA GrantPlan for Investigators)
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