Director / Sr. Director of Clinical Evidence Generation
Arima Genomics
Расположение работы
Carlsbad, CA, United States
Статус занятости
на постоянной основе
Подробности вакансии
Role: Director / Sr. Director of Clinical Evidence Generation
Location: Carlsbad, CA (Preferred) / Remote
Company Description:
Arima Genomics is a Carlsbad, CA biotechnology company with a proprietary 3D-genomics technology that reveals the organization of DNA at the cellular level. This technology is the basis of a CLIA-certified clinical testing service for the identification of gene fusions and rearrangements in patients with solid tumors.
Just like our technology is on another level, so are we. We are self-reflective and accountable self-starters who are tenacious and relentless in the pursuit of excellent products and services.
Our environment is open and collaborative, we invest in each other’s growth, and we empower one another. We listen to and value differences in perspective and approach. As a startup, we move fast, adapt to change and are continuously improving ourselves, our processes, and our products. Though we are adaptable we continuously prioritize to stay focused on our vision.
Duties
• Lead the planning and execution of clinical collaboration programs, building strong relationships with academic institutions, research collaborative groups, and large community practices in oncology
• Be accountable for effective program management of clinical program deliverables, including study protocols and other study documents, contracts, timelines, budgets, and resourcing and risk management plans, and for communicating progress to the executive team
• Closely coordinate with cross-functional teams (e.g. sales, marketing, research, development, legal, laboratory operations) to coordinate the planning, execution, and management of clinical studies and collaborations
• Other related duties as directed
Minimum Qualifications
• Advanced scientific or medical degree or equivalent (PhD, PharmD, MD, DO, NP/PA, or non-US equivalent)
• Experience leading clinical research and clinical trials conducted in genomics, diagnostics, oncology, or other applied medical fields
• Industry experience within CLIA laboratories highly preferred; IVD, pharmaceutical, biologics or medical device experience can substitute in part for CLIA experience.
• Understanding of the US healthcare system and academic institutional settings with demonstrated ability to navigate and lead through an ambiguous and changing healthcare and business environment
• Proficient at building credibility with investigators & collaborative research partners
• Ability to balance business and scientific acumen during engagements
• Knowledge of evidence-based medicine concepts, applied biostatistics and health economics are desirable
• Demonstrated organizational skills to manage multiple projects simultaneously, prioritize projects effectively and communicate at all levels within the company
• Strong written and verbal communication skills (including presentation skills)
• Proficient in Microsoft Office programs, such as Word, Excel, and PowerPoint
• Authorization to work in the United States without sponsorship
