23 часа назад
Senior Director, Clinical Science (Oncology)
276 000 - 341 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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