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2 часа назад

Senior Clinical Scientist (Oncology)

150 000 - 200 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Clinical Scientist (Oncology) (Clinical Development): Designing, executing, and interpreting Phase 1–3 oncology clinical trials with an accent on protocol development, clinical data quality, and biomarker-driven development. Focus on leading cross-functional trial execution, interpreting safety, efficacy, PK/PD, and biomarker data, and preparing regulatory submissions and clinical study reports.

Location: 100% remote within the United States

Compensation: $150,000–$200,000 per year, depending on experience, qualifications, and location.

Company

hirify.global Therapeutics is a clinical-stage oncology biotech company developing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program, for late-stage development.

What you will do

  • Lead the design and development of clinical protocols, amendments, and core study documents, including IBs, DSURs, SAPs, and CRFs.
  • Review, monitor, query, and interpret clinical data covering safety, efficacy, PK/PD, and biomarker endpoints.
  • Provide scientific leadership across clinical programs, including lifecycle planning and Phase 1–3 trial execution.
  • Collaborate with Clinical Operations and serve as the primary clinical contact for CROs, vendors, and investigative sites.
  • Identify study risks, drive issue resolution, and oversee data cleaning, query resolution, and database lock.
  • Lead contributions to regulatory submissions, clinical study reports, abstracts, manuscripts, and conference presentations.

Requirements

  • 5–8+ years of oncology clinical development experience.
  • Experience leading components of interventional Phase 1–3 clinical trials.
  • Strong expertise in clinical trial design, execution, and data interpretation.
  • Deep understanding of oncology drug development and working knowledge of GCP, ICH guidelines, and global regulatory requirements.
  • Ability to lead cross-functional initiatives, influence without authority, and communicate effectively in a fast-paced biotech environment.
  • Must be eligible to work in the United States; employment offers are contingent on verification of work eligibility.

Nice to have

  • Experience in metabolism, nutrition, or biomarker-driven approaches.
  • Advanced degree such as a PhD, PharmD, MS, or equivalent in life sciences, clinical research, or a related field.

Culture & Benefits

  • 100% remote work with a flexible schedule.
  • Health, dental, and vision coverage for employees and dependents.
  • Flexible time off and generous parental leave.
  • Traditional and Roth 401(k) plans.
  • Equity in a well-funded, clinical-stage biotech and a mission-oriented remote-first culture.

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