Director, Clinical Scientist

🕒 September 4

🇺🇸 United States – Remote

💵 $225k - $265k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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BBOT

WebsiteLinkedInAll Job Openings

51 - 200 employees

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

BBOT is a biotechnology company developing targeted therapies for cancers driven by RAS signaling and PI3Kα. The company focuses on rational drug design to inhibit the active ON state of RAS and to selectively block RAS-driven PI3K activation, aiming at multiple KRAS mutants and novel approaches to maximize target inhibition. BBOT translates decades of RAS biology research into therapeutic candidates intended to improve outcomes for patients with RAS- and PI3Kα-driven tumors.

📋 Description

• Support the Medical Monitor or serve as clinical lead for assigned Phase 1a/1b studies and future late-stage programs • Contribute to or oversee study start-up, site activation, enrollment, medical monitoring, data cleaning, data analyses, and clinical study report writing • Author, review, and maintain study protocols, protocol amendments, investigator brochures, informed consent forms, and clinical study reports • Partner with investigators and CROs to design and implement clinical studies • Provide scientific and medical input into study design, endpoints, inclusion/exclusion criteria, dose escalation schemas, and stopping rules • Conduct investigator meetings, safety review committee meetings, and site initiation visits • Serve as a primary medical point of contact for clinical site investigators and study teams • Contribute to clinical development plans, contingency plans, and program strategy • Provide technical and scientific input to meet program milestones and budgets • Translate preclinical and non-clinical findings into clinical development hypotheses and opportunities • Integrate emerging clinical data to inform ongoing study strategy and reverse translation • Interact with clinical investigators, thought leaders, and cooperative groups • Represent BBOT at scientific conferences and investigator meetings • Ensure clinical trial activities comply with ICH-GCP, applicable regulatory guidelines, and BBOT SOPs • Support audit and inspection readiness • Collaborate cross-functionally with Clinical Operations, Regulatory Affairs, Clinical Pharmacology, Translational Medicine, Biostatistics, and Safety for integrated program execution

🎯 Requirements

• Ph.D. or Pharm.D. in a relevant scientific or clinical discipline, with at least 3 years of oncology clinical development experience in a pharmaceutical or biotechnology industry setting • Other related scientific or clinical degrees with at least 5-8 years of oncology clinical development experience in a pharmaceutical or biotechnology industry setting, or an M.D. with clinical development experience will also be considered • Experience across all aspects of protocol conduct in early-phase oncology, including protocol writing, study start-up, execution, data analysis, and reporting • Ability to collaborate across multiple functions in a team environment, including Clinical Operations, Regulatory Affairs, Translational Medicine, and Clinical Pharmacology • Strong written and oral communication skills, including experience writing clinical documents (protocols, IBs, CSRs) and presenting data to internal and external audiences • Solid analytical and critical thinking skills; ability to interpret and synthesize complex clinical data and translate findings into clear, actionable recommendations • Demonstrated record of delivering results in compressed timelines; capable of prioritizing tasks and maintaining high-performance standards and attention to detail • Deep commitment to improving the lives of patients and a passion for developing novel therapeutics in oncology • Motivation to work in a fast-paced, high-accountability, small-company environment; collegial professionalism, interpersonal skills, intellectual curiosity, initiative, and ability to challenge assumptions and identify new approaches to complex problems • Prior experience in a lean or startup biotech environment is highly desirable • Ability and willingness to travel domestically and internationally to attend scientific conferences and clinical study sites as needed • Compliance with ICH-GCP, applicable regulatory guidelines, and BBOT SOPs

🏖️ Benefits

• Annual performance bonus • Company equity • Comprehensive health benefits