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Medical Director, Clinical Development (Oncology)

255Β 000 - 335Β 000$
Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
remote (Ρ‚ΠΎΠ»ΡŒΠΊΠΎ USA)/hybrid
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
director
Английский
b2
Π‘Ρ‚Ρ€Π°Π½Π°
US
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

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TL;DR

Medical Director, Clinical Development (Oncology): Lead execution of oncology clinical programs with an accent on medical monitoring of active trials and developing clinical development strategy. Focus on designing study protocols, collaborating with cross-functional teams, and interfacing with regulators and stakeholders to advance cell therapy products.

Location: Remote in South San Francisco, CA with frequent travel to South San Francisco or Los Angeles offices. Candidates must be authorized to work in the U.S.

Salary: $255,000–$335,000 per year

Company

Clinical-stage biotechnology company pioneering allogeneic CAR T cell (AlloCAR T) therapies for cancer and autoimmune diseases.

What you will do

  • Lead medical monitoring and study execution for oncology trials from pre-IND through late-stage development.
  • Develop and drive clinical development strategy aligned with portfolio goals.
  • Collaborate with multidisciplinary teams on trial design, execution, analysis, and reporting.
  • Define protocols, recommend sites/investigators, and manage interactions with regulators, CROs, and vendors.
  • Interface with scientists, clinicians, and stakeholders to identify opportunities and optimize strategies.
  • Represent the company at regulatory meetings and contribute to pipeline prioritization.

Requirements

  • Medical Degree, residency, and fellowship in oncology with 5+ years post-graduate experience in biotech/pharma (industry preferred).
  • Experience in hematology/oncology required; cell therapy highly preferred.
  • Strong knowledge of oncology drug development, IND/CTA filing, GxP (GCP/GLP), and regulatory inspections.
  • Ability to manage CROs/vendors within budgets and deliver under aggressive timelines.
  • Excellent communication and organizational skills for cross-functional collaboration.
  • Authorized to work in the U.S.

Culture & Benefits

  • Collaborative environment with talented team focused on delivering life-saving cancer therapies.
  • Competitive compensation including annual bonus, equity, and health insurance.
  • Generous time off with 2 annual company-wide holiday shutdowns.
  • Emphasis on accountability, positive attitude, and mission-driven work.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’