Full-Time

Senior Medical Director Hematology/Oncology

Sana Biotechnology

Sana Biotechnology

201-500 employees

Engineers cells as medicines for untreatable diseases

Biotechnology

$325,000 - $375,000

Health coverage, Paid time off, Disability insurance, Life insurance, Financial wellness programs, 401(k) Plan with an immediately vested employer match, Tuition Reimbursement and Student Loan Repayment, Employee Stock Purchase Plan, Commuter subsidy, Wellness offerings

Senior, Expert

Cambridge, MA, USA + 3 more

Required Skills
Communications
Marketing
Requirements
  • MD degree with a minimum of 7 years of combined medical practice and biotechnology or pharmaceutical industry experience in Clinical Research
  • Prior experience in Hematology and Oncology with board certification in one or both specialties
  • Deep understanding of and direct clinical experience in the treatment of B cell malignancies
  • Prior industry experience as a medical monitor contributing to the preparation of clinical protocols, study reports, IND, IB, NDA/CTD documents
  • Knowledge of GCPs, ICH guidelines and FDA regulations and familiarity with EMA/CHMP regulations and guidelines, and other international regulatory requirements
  • Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication
  • Demonstrated ability as a medical expert in a complex matrix environment
Responsibilities
  • Medical oversight for planned and future clinical trials throughout conduct and support of all medical and scientific aspects of clinical trial (s) and program level activities as assigned
  • Ensure appropriate scientific rigor in the design, conduct, validity, and interpretation of clinical trials using CAR-T therapies in B cell malignancies to support regulatory applications or future business/marketing objectives
  • Contribute to the strategic planning, authoring, and review of regulatory documents, scientific data disclosures, and commercial support documents
  • Conduct and have oversight over medical monitoring activities and co-lead interactions with the Data Safety Monitoring Committee
  • Identify significant issues that may impact overall project plans and initiate contingency plans as appropriate
  • Provide medical expertise and support to externally facing groups/stakeholders, including the field medical team, medical information and the commercial organization
  • Maintain close collaboration and cooperation with clinical operations on the implementation and execution of clinical studies
  • Contribute and be responsible to the development planning, authoring and review of manuscripts and other scientific data disclosures
  • Contribute to departmental resource planning, budgeting and timeline setting to meet company needs
  • Serve as a medical interface to key opinion leaders (KOL), facilitating KOL advocacy development
  • May provide oversight and coaching to more junior clinical research staff

Sana Biotechnology, Inc. stands out as a leading company in the cell and gene therapy industry, with a unique focus on using engineered cells as medicines to treat diseases with poor outcomes or that are currently untreatable. Their competitive edge lies in their advanced delivery technologies, their ability to differentiate pluripotent stem cells into immune-cloaked functional cells, and their commitment to scalable manufacturing solutions. The company's culture is deeply rooted in impacting patients' lives, as evidenced by their ongoing development of diverse drug candidates aimed at broadening treatment possibilities.

Company Stage

IPO

Total Funding

$865M

Headquarters

Seattle, Washington

Founded

2018

Growth & Insights
Headcount

6 month growth

-13%

1 year growth

-18%

2 year growth

-9%
INACTIVE