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23 часа назад

Senior Director, Clinical Science (Oncology)

276 000 - 341 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior/director
Английский
c1
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 Director, Clinical Science (Oncology): Leading clinical science activities for early oncology development programs, including protocol design, clinical data review, regulatory documents, and study reporting with an accent on patient safety, medical monitoring, and cross-functional clinical development. Focus on interpreting safety data, supporting Phase 1 trials, preparing health authority submissions, and presenting results to investigators, committees, and scientific meetings.

Location: South San Francisco, California, United States; onsite four days per week with work-from-home flexibility

Salary: $276,000–$341,000 per year

Company

hirify.global is a precision medicine oncology company developing targeted therapies for genetically defined solid tumors, including small-molecule and antibody-drug conjugate programs.

What you will do

  • Develop clinical concepts and plans for molecules across development stages, with a focus on early oncology.
  • Write and review protocols, protocol amendments, informed consent forms, investigator brochures, and clinical sections of regulatory submissions.
  • Represent the clinical function on study teams and partner with Clinical Operations on site selection, study start-up, and communications.
  • Review and interpret safety data, serious adverse events, clinical study reports, and clinical program summaries.
  • Support Phase 1 medical monitoring, patient safety activities, health authority interactions, inspections, audits, updates, and submissions.
  • Present clinical data, train colleagues and study personnel, participate in advisory boards, and contribute to publications and scientific meetings.

Requirements

  • Bachelor’s degree and strong knowledge of clinical oncology gained through clinical development experience.
  • At least four years of industry experience in oncology and previous participation in clinical development programs.
  • Experience with protocol design, clinical data interpretation, medical monitoring, adverse-event assessment, and patient safety.
  • Knowledge of Good Clinical Practice and excellent written and oral communication skills.
  • Fluency in English is required.
  • Ability to work onsite in the South San Francisco office four days per week is required.

Nice to have

  • Postgraduate qualification in clinical oncology, or an MD, Nurse Practitioner’s License, PharmD, or PhD.
  • Experience with small-molecule clinical trials and involvement across all trial stages from start-up through study reporting.
  • Background in clinical operations, regulatory affairs, or biometrics with clinical team-level experience.

Culture & Benefits

  • Collaborative, inclusive, data-driven environment focused on precision oncology and patient outcomes.
  • Medical, dental, and vision coverage, with 100% employee and 90% dependent premiums paid by the company.
  • 401(k), employee stock purchase plan, wellness programs, and potential merit increases, short-term incentives, and stock options.
  • Work-from-home flexibility alongside required office attendance.
  • Employees working in company facilities must be fully vaccinated, subject to applicable accommodations.

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