Medical Director - Clinical Development - Oncology
ExternalPrepare for this interview
EliteAI-generated questions, company research, and talking points tailored to this role
Requirements
- MD, DO or equivalent degree. Board certification or eligibility in Oncology or Internal Medicine preferred
- 3+ years of clinical development and leadership experience in the pharmaceutical or biotechnology industry
- Proven track record in the design, execution, and analysis of Phase 1-2 clinical trials
- Excellent communication, presentation, and interpersonal skills, capable of influencing strategy across all levels of the organization
- Experience with biologic agents (mAb, ADC, TCE)
- Experience leading regulatory interactions (FDA, Health Canada, EMA)
- Experience with translational medicine and biomarker development
Benefits
Additional Information
Each of us cares about someone who will need medicines. That's why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown. We are seeking a Medical Director to join our Clinical Development team, to drive clinical strategy for our oncology pipeline. You will provide medical and scientific leadership for early oncology programs from pre-IND/CTA stage through Phase 1-2 including study design and execution, medical monitoring, interpretation and reporting of the clinical trial results with the highest standards for safety and regulatory compliance. How you will make an impact: Lead the medical strategy for assigned oncology programs Author clinical protocols (Phase 1-2), contribute to investigator brochures, IND/CTA submission, clinical study reports (CSRs), and regulatory documents throughout the program lifecycle Serve as the Medical Monitor for assigned trials, overseeing patient eligibility, safety, and protocol adherence Interpret clinical trial data, including safety, efficacy, PK, PD, and translating findings into actionable development strategy Ensure all clinical development activities are conducted in accordance with GCP, regulatory requirements, and company SOPs Serve as the primary clinical contact for assigned programs to internal teams, external investigators, and regulatory agencies Establish and maintain a collaborative relationship with medical experts and investigators in the assigned therapeutic area of developmen Collaborate closely with cross-functional teams, including Translational Science, Clinical Operations, Regulatory Affairs, Biostatistics, and Corporate Development Develop publications, and present data and strategy to governance committees and at external meetings
Your Match
How well this role fits your profile.
Company Intel
What employees say
Worked at abcellera? Share your experience