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Job Description
About the Role
Provide medical leadership for Phase 3 oncology trials. Oversee protocol development, safety monitoring, and regulatory submissions. Serve as clinical representative to health authorities and scientific advisory boards.
Responsibilities
- Lead medical strategy for oncology pipeline
- Review and approve clinical study protocols
- Oversee safety surveillance and pharmacovigilance
- Interpret clinical data for regulatory submissions
- Mentor medical monitors and clinical scientists
- Represent company at FDA advisory meetings
- Author manuscripts for publication
Requirements
- MD (Board Certified in Oncology)
- Active medical license
- 8+ years clinical research experience
- Oncology therapeutic expertise
- FDA regulatory submission experience
- Publications in peer-reviewed journals
- Knowledge of GCP/ICH guidelines
- Phase 3 trial leadership experience
Benefits
- Annual bonus (30-40% of base)
- Full malpractice insurance coverage
- Continued medical education allowance ($15K/year)
- Flexible clinical practice options (20% FTE)
- 401(k) with 8% company match
- Comprehensive health/dental/vision
- Relocation package available
About the Company
OncoTherapeutics is pioneering targeted cancer treatments with 3 therapies in late-stage development. Our science-driven culture brings together world-class researchers committed to extending patient survival. Recently secured $300M Series D funding for pipeline expansion.
Job ID: clinical-research-medical-director-qpIfi
