Contract Director/Sr. Director, Clinical Science (Early Oncology Development) at Scorpion Therapeutics | Torre
Contract Director/Sr. Director, Clinical Science (Early Oncology Development)
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Contract Director/Sr. Director, Clinical Science (Early Oncology Development)

Scorpion Therapeutics
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Full-time

Legal agreement: To be defined

Compensation
USD100 - 200/hour
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Remote (for San Francisco, CA residents)
Remote (for Boston residents)
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Posted about 2 years ago

Requirements and responsibilities

- Pioneering clinical-stage oncology company redefining the frontier of precision medicine - Proprietary and fully integrated platform of advanced technologies across cancer biology, medicinal chemistry, and data sciences - Broad pipeline of wholly owned, optimized compounds targeting validated oncogene targets, previously undruggable targets, and novel cancer targets Our Clinical Development team is seeking a Contract Director/Senior Director, Clinical Science (Early Development) to provide scientific and clinical expertise in the development, design, conduct, analysis, and reporting of global clinical trials. The ideal candidate will have experience in clinical research and/or drug development within the pharmaceutical industry, with a focus on oncology. This role requires a team-oriented, goal-driven, and highly collaborative individual with excellent written and oral communication skills. Responsibilities: - Contribute to oversight of trials in start-up, conduct, and close-out, for Phase I-III in close coordination with Clinical Operations - Participate in critical site-facing activities (PSVs, SIVs, etc.) and contribute to preparation of meeting materials in collaboration with the Clinical Trial Lead - Coordinate and conduct regular data/safety/efficacy reviews and identify trends across programs in collaboration with the Global Medical Monitor - Contribute to the cross functional trial team as the clinical sciences lead - Participate with the study team to prepare for and execute regulatory milestones - Contribute to the development of study documents for activities around study conduct, regulatory requirements, and IDMCs - Work with statisticians/biometrics to develop the required tables/listings/figures and contribute to the interpretation of efficacy and safety data from clinical trials - Present safety findings and study status to internal stakeholders - Coordinate presentations at IDMC meetings, and other meetings, such as Investigator and Safety Review Meetings - Participate in various initiatives and duties as required by the clinical development program
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