AbCellera
Medical Director - Clinical Development - Endocrinology and Autoimmune Diseases
Vancouver · Director
Sponsorship not specifiedDetected 28 days ago
GCPClinical TrialsFDA RegulatoryExperimental DesignAnimal StudiesLeadershipCommunicationMentoringGxPBiostatisticsRegulatory Affairs
About the role
- Each of us cares about someone who will need medicines.
- We pursue truth and scientific rigour and have the courage to work at the edge of the unknown.
- Scientific and technical mentorship is a priority.
Responsibilities
- We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.
- We look for people with drive and energy.
- Designing and authoring clinical protocols (Phase 1-3), investigator brochures, clinical study reports (CSRs), and regulatory documents (IND, CTA)
- Developing publications, present data and strategy to governance committees and at external meetings
Compensation
- In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution.
Benefits
- AbCellera's hiring range for this role is currently under review and will be commensurate with your education and job-related knowledge, skills, and experience.
- In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution.
- You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits.
- We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women's health, immunology, and oncology.
- We believe that when tenacious people share a vision and work together, they can truly have a positive impact.
- Leading the medical strategy for assigned clinical development programs in endocrinology and/or autoimmune diseases
- Serving as the Medical Monitor for assigned trials, overseeing patient eligibility, safety, and protocol adherence
- Providing medical expertise for the ongoing assessment and management of patient safety, including reviewing cumulative safety data, serious adverse events (SAEs) and contributing to safety reports (DSURs)
- Establishing and maintaining collaborative relationship with medical experts and investigators in the assigned therapeutic areas of development
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