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 Clinical Demand and Supply Manager who will be responsible for the end-to-end management of Investigational Medicinal Product (IMP) and ancillary supplies for global clinical trials. In this role, you are responsible for ensuring the right product is in the right place, at the right time, and in the right condition for our clinical studies and patients. You are a strong collaborator and will work extensively with cross-functional teams, including Clinical Operations, CMC, Quality Assurance and Regulatory Affairs, as well as manage external partners (CMOs, depots and couriers) to execute flawless clinical supply strategies. 

How you might spend your days

• Developing and maintaining global supply plans for clinical trials, including demand planning forecasts across AbCellera’s programs
• Managing and maintaining global inventory across all central depots and clinical sites, ensuring uninterrupted supply while utilizing ERP/inventory systems for accurate record keeping
• Managing packaging, labelling, and distribution activities with CMO partners
• Coordinating global shipments of clinical supplies, ensuring strict compliance with international trade regulations, import/export requirements, and customs documentation
• Managing and qualifying temperature-controlled shipments (cold chain), collaborating  with Quality Assurance to resolve any temperature excursions
• Collaborating with teams and vendors to set up, manage and lead  User Acceptance Testing (UAT) for Interactive Response Technology (IRT/IXRS) systems governing inventory, randomization, and drug assignment
• Ensuring all clinical supply activities strictly adhere to Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and global regulations
• Acting as the Clinical Supply Subject Matter Expert on clinical study teams, collaborating with CMC, Regulatory Affairs (label approvals/submission requirements), and Clinical Operations
• Overseeing drug accountability, returns, and destruction, ensuring complete documentation, and assisting in the developing and managing of the clinical supply budget for assigned studies

We'd love to hear from you if

• You have demonstrated expertise in cGMP, GCP, and global clinical trial regulations (e.g., FDA, EMA) as well as experience managing packaging, labeling, and distribution partners (CMOs and all external partner organizations)
• You have a Bachelor’s degree in a scientific discipline, Supply Chain Management, or a related field, plus 8+ years of relevant work experience in the pharmaceutical or biotechnology industry, with at least 3 years in a direct clinical supply chain role
• You have hands-on experience with Interactive Response Technology (IRT/IXRS) systems is essential
• You have proven ability to manage complex, temperature-controlled (cold chain) logistics

What we offer

AbCellera’s hiring range for this role is CAD $124,560 - $155,700 annually, 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. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

Our headquarters is in Vancouver and working on site is highly desirable. For this position, remote applications will be considered. 

About AbCellera

Creating medicines is the most important work we can do. 

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 have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23337 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 looking for an Associate Director, CMC Regulatory Affairs (RA) who will work closely with our manufacturing and quality teams to develop and implement global CMC strategies for multiple biologics programs, from pre-clinical through Phase 3 studies. You will be a key member of project teams, shaping the CMC RA strategy and documentation for innovative new biologics and ensuring submissions are aligned with health authority requirements and delivered on time with quality.

How you might spend your days:

• Serving as the primary CMC regulatory representative in project meetings and with regulatory agencies 
• Preparing CMC regulatory submissions including briefing documents, IND submissions, and CTA filings 
• Overseeing the preparation of responses to regulatory authority queries
• Managing critical CMC regulatory timelines, working with team members to navigate the pathways for manufacturing and analytical development, working in close partnership with the CMC and Quality teams 
• Staying on top of detailed knowledge of the global regulatory environment relevant for biologics, communicating changing regulatory agency requirements, and supporting pertinent regulatory intelligence per needs of programs
• Collaborating with external consultants, CDMOs, and CROs to provide regulatory guidance
• Evaluating regulatory CMC program risks and establishing mitigation strategies pertinent to product development
• Partnering with CMC, Discovery, and Clinical Development teams to innovate strategies to accelerate submission timelines 

We'd love to hear from you if:

• You have a deep understanding of CMC regulatory requirements, eCTD structure, and Module 3 preparation (BLAs/NDAs/NDSs) for biologics and combination products
• You can seamlessly navigate regulatory requirements for CMC submissions for biologics and combination products, and look forward to the preparation of regulatory submissions
• You have a thorough understanding of Health Canada, FDA, and EMA regulations 
• You can efficiently oversee independent contractors and vendors
• You are a skilled regulatory writer with effective oral communication skills
• You are a detailed oriented individual, highly organized, and thrive in fast paced environments while managing multiple priorities.
• You have a relevant post-secondary degree(s) in biological, pharmaceutical, chemical, engineering sciences or a related field, plus about 12 years of relevant work experience

What we offer:

AbCellera’s hiring range for this role is CAD $141,000 - $170,000 annually, 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. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera:

Creating medicines is the most important work we can do. 

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 have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply:

Please submit your application through our website and refer to Job ID 23350 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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 provide medical and scientific leadership for our pipeline programs in the areas of endocrinology and autoimmune diseases from pre-IND/CTA stage through Phase 1/FIH and later stage trials. You will lead the cross-functional program team and drive the development strategy, including study design, execution, interpretation, and reporting of clinical trials, ensuring the highest standards of safety and regulatory compliance.

How you might spend your days

• Leading the medical strategy for assigned clinical development programs in endocrinology and/or autoimmune diseases
• Designing and authoring clinical protocols (Phase 1-3), investigator brochures, clinical study reports (CSRs), and regulatory documents (IND, CTA)
• Serving as the Medical Monitor for assigned trials, overseeing patient eligibility, safety, and protocol adherence
• Interpreting clinical trial data, including safety, efficacy, and pharmacokinetics/pharmacodynamics (PK/PD), and translate findings into actionable development strategy
• 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)
• Ensuring all clinical development activities are conducted in accordance with Good Clinical Practice (GCP), relevant regulatory requirements, and company standard operating procedures (SOPs)
• Serving as the primary clinical contact for assigned programs to internal teams, external investigators, and regulatory agencies
• Establishing and maintaining collaborative relationship with medical experts and investigators in the assigned therapeutic areas of development
• Collaborating closely with cross-functional teams, including Translational Science, Clinical Operations, Regulatory Affairs, Biostatistics, and Corporate Development
• Developing publications, present data and strategy to governance committees and at external meetings

We’d love to hear from you if

• You have an M.D. (Doctor of Medicine) or equivalent degree; Board Certification or eligibility in Endocrinology, Rheumatology, or Internal Medicine is preferred
• You have 12+ years of clinical development and leadership experience in the pharmaceutical or biotechnology industry
• You have a proven track record in the design, execution, and analysis of Phase 1-2 clinical trials
• You have excellent communication, presentation, and interpersonal skills, and are capable of influencing strategy across all levels of the organization
• You have experience with biologic agents (such as monoclonal antibodies), and/or novel modalities (bispecifics, T-cell engagers, ADC)
• You have experience interacting with major regulatory agencies (FDA, Health Canada, EMA)
• You have experience with translational medicine and biomarker development in clinical trials

What we offer

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. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera

Creating medicines is the most important work we can do. 

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 have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply

Please submit your application through our website and refer to Job ID 23331 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.

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

Who you are:

• 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

What we offer:

AbCellera’s hiring range for this role is CAD $280,000 - $325,000 annually, commensurate with your education 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. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials.

About AbCellera:

Creating medicines is the most important work we can do. 

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 have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline.

Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.

We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. 

We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.

To apply:

Please submit your application through our website and refer to Job ID 23347 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.