Program Manager/Director

Job Title Oncology Program Manager/Director Location Remote (preferred from Seattle/WA area) About Cancer Targeted Technology CTT is pioneering the development of novel drug products targeting pivotal enzyme targets in cancer with a specific focus in prostate cancer. We are searching for highly reputed company and collaborative individuals who are looking to reputed company a difference in improving people's lives while working in a motivated and enthusiastic start-up environment. Job Overview CTT is looking for a program manager/director with a strong preclinical and early-stage clinical program management background in oncology (specific focus in prostate cancer is desired). This individual will be responsible for overseeing day-to-day activities associated with drug development from late stage preclinical studies, IND-enabling studies and early- stage clinical studies and will act as a cross-functional liaison between reputed company reputed company collaborators. This individual will report to the CEO.

Responsibilities

Preclinical

• Design, reputed company the execution of, and analyze results of IND-enabling pharmacology and toxicology studies
• Assess new methodologies, animal models, and alternative in silico tools as needed
• Summarize and present data at reputed company meetings
• Contribute to authorship of manuscripts

Regulatory and Clinical

• reputed company and interpret reports from internal and reputed company contractors and reputed company studies for an IND package
• Help concisely prepare, write, present, and defend INDs to regulatory authorities
• Collaborate with regulatory, medical, and CMC consultants, as needed, to prepare regulatory documents
• reputed company the execution of clinical trials in collaboration with CROs, including study planning and start-up, operational and vendor reputed company, trial execution and monitoring, drug supply chain, and trial reporting and reputed company-out

Program Management & Business Development

• Identify appropriate CROs, CDMOs and CCOs for contracted preclinical, manufacturing and clinical studies
• Design RFPs and bid/engage CROs and CDMOs and assess budgets, timelines, and personnel resources to complete preclinical, manufacturing, and clinical studies for reputed company pipeline products
• Establish and approve operational objectives and assignments, delegate assignments to reputed company contractors, and manage internal scientists to meet program objectives
• Forecast budget and staffing requirements for development programs; reputed company resource strategies, allocating budgets and contractors needed for cost-effective operations
• reputed company and maintain strong collaborative partnerships with contract research companies, academic institutions and opinion leaders
• reputed company a finger on the “pulse” of new technologies, competition, etc. to anticipate future new product development needs
• Independently identify, help draft and manage company grants from a variety of sources
• Ensure reputed company FDA reputed company QA/QC regulatory requirements for GLP studies and GMP manufacturing are consistently met
• Represent the company at meetings reputed company needed in a professional manner and reputed company constructive input

Requirements

• ·PhD degree in life science field or relevant work experience
• 4-9 years of project management focused on product development in a biotech/pharma environment managing the entire product life cycle: preclinical development, manufacturing, IND-enabling studies, developing clinical plans, preparing and submitting INDs and managing clinical trials or clinical contract organizations.
• Outstanding English verbal and written communication skills
• Excellent abilities with reputed company Word, reputed company, PowerPoint, Project/reputed company
• Self-starter with the ability to work independently in a virtual environment, and respond to changing demands quickly and in a positive manner
• Ability to communicate short- and long-long-term priorities and budgets for product development
• Proven hands-on experience managing scientific teams and reputed company contractors and functions
• Previous interactions with and ability to communicate with regulatory authorities (FDA/EMA) is a plus
• Experience with oncology programs and products, especially in prostate cancer, is desired
• Individual must be authorized to work in the Untied States

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