Radiopharma Clinical Development Lead - HCC & GI

Bristol-Myers Squibb Co

United States

Teletrabalho

USD 307 000 - 372 000

Tempo integral

14 dias+

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

Ultrapassa os filtros ATS

Vantagens oferecidas por esta oferta de emprego

Health Coverage
401(k) plan & disability coverage
Paid time off

Resumo da oferta

RayzeBio, a Bristol Myers Squibb subsidiary, seeks a Sr Medical Director in Radiopharmaceuticals to oversee clinical development for HCC and GI cancers from IND to Phase 3. You will lead cross-functional teams, interact with investigators, and guide regulatory interactions while shaping strategy.

The role requires an MD with oncology subspecialty and 5+ years in oncology biotech/pharma, with radiopharmaceutical experience preferred.

Qualificações

  • MD with oncology sub-specialty training required.
  • 5+ years in oncology solid tumor clinical development.
  • Radiopharmaceutical experience preferred but not required.
  • Expertise in HCC and GI cancers required.
  • Strong collaboration and communication across functions.

Responsabilidades

  • Support IND preparation and regulatory interactions.
  • Design and oversee Phase 1–3 trials and medical monitoring.
  • Lead cross-functional study teams and collaborate with investigators/CROs.
  • Translate findings into clinical development opportunities.
  • Engage with regulatory bodies and prepare briefing documents.
  • Travel approximately 30% of the time.

Conhecimentos

Patient-focused
Collaborate across functions
Written and oral communication
Strategic & analytical thinking
Leadership through influence
Priority management

Formação académica

MD with oncology subspecialty

Descrição da oferta de emprego

RayzeBio, a Bristol Myers Squibb subsidiary, seeks a Sr Medical Director in Radiopharmaceuticals to oversee clinical development for HCC and GI cancers from IND to Phase 3. You will lead cross-functional teams, interact with investigators, and guide regulatory interactions while shaping strategy.

The role requires an MD with oncology subspecialty and 5+ years in oncology biotech/pharma, with radiopharmaceutical experience preferred.

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