Senior Director, Clinical Science
$276,000–$341,000 year
HybridSouth San Francisco, California, United States
Job Summary
Develop clinical development concepts and plans for oncology molecules, drafting protocols, amendments, and informed consent forms while partnering with Clinical Operations on site selection. Represent the medical function on study teams, review safety data and serious adverse events, and serve as primary author for clinical study reports and publications. Lead the creation of investigator brochures, present results to internal committees and external advisory boards, and build networks with opinion leaders and investigators. Support Health Authority interactions, audits, and submissions, and act as Medical Monitor for Phase 1 trials, guiding design, execution, and reporting. Contribute to therapeutic area research, competitor analysis, and program-level activities including risk management plans and periodic safety updates.
Required Qualifications
- Bachelor's degree
- Strong knowledge of clinical oncology
- Previous clinical development experience
- Postgraduate qualification in clinical oncology (e.g., Masters degree)
- MD, Nurse Practitioner's License, PharmD or PhD
- At least 4 years of industry experience in oncology
- Previous participation in a clinical development program
- Involvement in all stages of clinical trials (i.e., from start up to study report)
- Experience in clinical trials with small molecules
- Skilled in protocol design, interpretation, and medical monitoring
- Experience in assessment of adverse events and safety of patients participating in therapeutic clinical trials
- Knowledge of Good Clinical Practice
- Excellent written and oral communication
- Capacity to adapt to a fast-paced and changing environment
- Fluency in English
- Good judgement and ethical behavior
- Maintain patient and product safety as a top priority
- Report any suspected violations of law or Company policy through appropriate channels
- Fully vaccinated from COVID-19
- Work onsite in the office four days per week
Desired Qualifications
- Postgraduate qualification in clinical oncology (e.g., Masters degree)
- MD, Nurse Practitioner's License, PharmD or PhD
- Previous participation in a clinical development program
- Involvement in all stages of clinical trials (i.e., from start up to study report)
- Experience in clinical trials with small molecules
- Experience in assessment of adverse events and safety of patients participating in therapeutic clinical trials
- Candidates with a background in closely related functions (e.g., clinical operations, regulatory affairs, biometrics), having represented their function at project/clinical team level
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