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 experienced, strategically minded Principal Scientist to join our expanding Non-Clinical Safety team based in Vancouver, Canada. You will be responsible for designing, planning, monitoring, and reporting of non-GLP and GLP toxicology studies and provide nonclinical safety support for early to late stage programs. 

How you might spend your days

• Leading the planning, design, execution and interpretation of nonclinical toxicology programs in support of IND, CTA and BLA submissions, including general toxicity and reproductive and developmental toxicology studies, in alignment with global regulatory expectations and program strategy
• Serving as the primary scientific interface with contract research organizations (CROs), providing strategic oversight during protocol development, study conduct, data interpretation, and report finalization to ensure timely, high-quality, and GLP-compliant delivery of nonclinical studies
• Representing the Nonclinical Safety function as a core member of cross-functional discovery and development program teams, contributing toxicology expertise to inform candidate selection, risk assessment, and overall program advancement
• Providing critical scientific assessment of toxicology data and communicating clear, actionable risk-benefit evaluations and recommendations to project teams and senior leadership, including potential implications for clinical development and regulatory strategy 
• Authoring and reviewing nonclinical safety sections of regulatory documents (INDs, CTAs, IBs, and BLAs), and contributing as a subject matter expert to global regulatory interactions and health authority responses
• Driving the development and evolution of integrated nonclinical safety strategies across AbCellera’s therapeutic portfolio, ensuring consistency, scientific rigor, and alignment with company objectives
• Maintaining scientific leadership by staying current with advances in toxicology science, methodologies, and evolving regulatory guidance, and proactively translating these insights into best practices for internal programs

We'd love to hear from you if

• You bring deep expertise in GLP-compliant nonclinical toxicology, including hands-on experience with US FDA 21 CFR Part 58, and a strong working knowledge of FDA, ICH, and EMA nonclinical regulatory guidance
• You have a proven track record of designing, overseeing, and interpreting non-GLP and GLP toxicology studies in support of discovery and development programs; experience with oncology and/or ADC programs is highly desirable
• You hold a PhD in Toxicology or a related field, with 8+ years of relevant industry experience supporting biologics development; candidates with a MSc degree and 12+ years of directly applicable experience will also be considered
• You demonstrate the ability to lead scientific discussions and influence decision-making within highly matrixed, cross-functional teams through clear, confident, and effective communication
• You possess excellent scientific writing skills, with experience authoring and reviewing toxicology reports and regulatory submission documents
• You exhibit strong organizational and prioritization skills, enabling effective management of multiple programs and timelines in a fast-paced environment
• You apply sound scientific judgment and critical problem-solving skills to assess complex datasets, identify risks, and propose strategic solutions
• You thrive in a dynamic, evolving environment, demonstrating flexibility, resilience, and a proactive approach to change
• You hold DABT accreditation (highly desirable, but not required)

What we offer

AbCellera’s hiring range for this role is CAD $134,000 - $168,000 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 23346 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 highly motivated and experienced Clinical Study Manager (CSM) to lead and manage clinical trials from start-up through to completion. Based out of Montréal, Québec, the Clinical Study Manager will ensure the efficient and timely execution of clinical studies in compliance with regulatory requirements, protocols, and standard operating procedures (SOPs). In this role, you will collaborate with cross-functional teams, including clinical research associates (CRAs), data managers, and regulatory personnel, to deliver high-quality clinical data while maintaining adherence to the budget and timelines.

How you might spend your days:

• Overseeing the global strategy of clinical trials, including study planning, execution, monitoring, and close-out 
• Ensuring clinical studies are conducted in accordance with the approved protocol, Good Clinical Practice (GCP), and applicable regulations
• Acting as the primary Sponsor contact for Global CRO Project Directors and Global functional leads
• Partnering with Clinical Project Managers (CPMs) to translate global recruitment targets into country-specific execution plans
• Developing and reviewing study plans, protocols, and related documents, while overseeing site selection, feasibility assessments, and the development of study materials
• Ensuring studies adhere to regulatory requirements and ethical standards, handling regulatory inspections and audits, and implementing corrective actions when necessary
• Developing and managing project timelines, milestones, and budgets, ensuring all deliverables are met within the agreed-upon timeframe and budget
• Identifying potential risks to the study, developing mitigation strategies, and taking appropriate action to resolve issues as they arise during the course of the study
• Overseeing the collection, analysis, and reporting of clinical trial data, ensuring data integrity and quality, accurate data handling, and compliance with data protection regulations
• Monitoring and ensuring the safety and welfare of study participants by adhering to safety reporting guidelines and promptly addressing any safety concerns

We'd love to hear from you if:

• You have a Master’s degree in a relevant field, and 6+ years of demonstrated work experience as a Regional Clinical Project Manager or Clinical Study Manager; candidates with a Bachelor’s degree and 8+ years of related experience will also be considered
• You have strong working knowledge of Good Clinical Practice (GCP), regulatory requirements, and clinical trial management
• You have previous experience as a CRA, or experience working at clinical sites
• You have strong organizational and project management skills, with the ability to prioritize and manage competing deadlines
• You are bilingual with excellent communication skills, both written and verbal, and have the ability to collaborate effectively with internal teams, external vendors, and clinical investigators
• You are proficient in clinical trial management systems (CTMS), electronic data capture (EDC) systems, and other relevant software
• You are certified in Clinical Research, such as ACRP, SOCRA (desirable)

What we offer:

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, opportunity for flexible work arrangements, 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 23359 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 motivated and meticulous individual, with extensive experience conducting in vivo studies in accordance with Animal Use Protocols and Standard Operating Procedures, to join our team. You will contribute to the discovery of therapeutic antibodies and subsequent efficacy assessments, and through teamwork, innovation, and mutual support, together we will tackle the most challenging scientific problems.

How you might spend your days: 

• Overseeing day-of-study activities; supporting efficient and high-quality study execution
• Collaborating with study leads, scientists, and cross-functional teammates, ensuring alignment on study protocols, animal welfare considerations, and animal macro- and micro-environment requirements of in vivo studies
• Providing technical support, troubleshooting, and problem-solving solutions, while identifying opportunities for process improvement and implementing best practices to optimize workflow efficiency
• Contributing to the preparation of Animal Use Protocols (AUPs) and Standard Operating Procedures (SOPs) to comply with CCAC Regulations and Guidelines
• Ensuring accurate recording of in vivo data across all studies, and supporting teammates with data analysis as required
• Training and mentoring team members to ensure compliance with safety policies, SOPs, and regulatory requirements
• Performing in vivo and ex vivo techniques to support study objectives, applying deep technical expertise in in vivo procedures
• Carrying out daily health assessments and clinical observations, ensuring high standards of animal welfare and accurate documentation
• Preparing and maintaining laboratory spaces, equipment, and consumables required for in vivo and ex vivo work
• Preparing and aliquoting reagents required for in vivo studies

We'd love to hear from you if:

• You provide the highest level of animal care while overseeing and performing in vivo activities
• You are experienced with animal handling, dosing (IV, IP, SQ), and blood collection, and have a strong understanding of the 3Rs and research ethics
• You have 6+ years of experience in an in vivo research environment; a BSc, MSc, and/or experience with in vitro and ex vivo techniques are considered assets
• Managing competing priorities comes with ease for you, and you thrive in a collaborative, fast-paced work environment
• You take pride in being a self-motivated person, fast learner, team player, and creative problem solver
• You have excellent communication, documentation, and organizational skills, and are known for your accountability and reliability
• You are able to lift up to 25 kg, and are comfortable with long periods of standing and bending throughout your day
• You are able to work at least one weekend day per week

What we offer:

AbCellera’s hiring range for this role is CAD $75,800 - $94,700 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, opportunity for flexible work arrangements, 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 23365 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 motivated and meticulous individual, with extensive experience conducting in vivo studies in accordance with Animal Use Protocols and Standard Operating Procedures, to join our team on either a Tuesday to Saturday or Sunday to Thursday work schedule. You will contribute to the discovery of therapeutic antibodies and subsequent efficacy assessments, and through teamwork, innovation, and mutual support, together we will tackle the most challenging scientific problems. 

How you might spend your days: 

• Performing in vivo and ex vivo techniques to support study objectives, applying deep technical expertise in in vivo procedures
• Carrying out daily health assessments and clinical observations, ensuring high standards of animal welfare and accurate documentation
• Contributing hands-on expertise during day-of-study activities, supporting efficient and high-quality study execution
• Preparing and maintaining laboratory spaces, equipment, and consumables required for in vivo and ex vivo work
• Troubleshooting technical challenges in real time, identifying opportunities to improve procedures and workflow efficiency
• Ensuring accurate and complete recording of in vivo study data, maintaining strong documentation and data integrity practices
• Sharing technical knowledge and best practices with team members, supporting strong adherence to SOPs, safety standards, and regulatory requirements
• Working closely with study managers and research teams to ensure alignment with study protocols and animal welfare consideration

We'd love to hear from you if:

• You provide the highest level of animal care while overseeing and performing in vivo activities
• You have strong expertise in  animal handling, dosing (IV, IP, SQ), and blood collection, and have a strong understanding of the 3Rs and research ethics
• You have 6+ years of experience in an in vivo research environment; a BSc, MSc and experience with in vitro, in vivo, and ex vivo techniques for PK and oncology models are considered assets
• Managing competing priorities comes with ease for you, and you thrive in a collaborative, fast-paced work environment
• You take pride in being a self-motivated person, fast learner, team player, and creative problem solver
• You have excellent communication, documentation, and organizational skills, and are known for your accountability and reliability
• You are able to lift up to 25 kg, and are comfortable with long periods of standing and bending throughout your day
• You are able to work at least one weekend day per week

What we offer:

AbCellera’s hiring range for this role is CAD $75,800 - $94,700 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, opportunity for flexible work arrangements, 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 23353 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 motivated and meticulous individual, with extensive experience conducting in vivo studies in accordance with Animal Use Protocols and Standard Operating Procedures, to join our team on either a Tuesday to Saturday or Sunday to Thursday work schedule. You will contribute to the discovery of therapeutic antibodies and subsequent efficacy assessments, collaborating with teammates through innovation, mutual support, and shared expertise. If you love contributing directly to in vivo research through hands-on lab work, this is the role for you! 

How you might spend your days: 

• Performing in vivo and ex vivo techniques to support in vivo studies 
• Carrying out daily health assessments and recording clinical observations
• Supporting in vivo day-of-study operations to ensure smooth execution and to maximize efficiency
• Organizing and preparing lab spaces, materials/consumables, and equipment for in vivo and ex vivo activities
• Providing technical support and problem-solving solutions, while identifying opportunities for process improvement and implementing best practices to optimize workflow efficiency 
• Ensuring accurate recording of in vivo data across all studies and supporting teammates with data entry as required
• Training and mentoring team members to ensure compliance with safety policies, SOPs, and regulatory requirements
• Collaborating with study managers, ensuring alignment on study protocols and animal welfare considerations

We'd love to hear from you if:

• You provide the highest level of animal care while overseeing and performing in vivo activities
• You are experienced with animal handling, dosing (IV, IP, SQ), and blood collection, and have a strong understanding of the 3Rs and research ethics
• You have 4+ years of experience in an in vivo research environment; a BSc, and experience with in vitro, in vivo, and ex vivo techniques for PK and oncology models are considered assets
• You manage competing priorities seamlessly and you thrive in a collaborative, fast-paced lab environment
• You take pride in being a self-motivated person, fast learner, team player, and creative problem solver
• You have excellent communication, documentation, and organizational skills, and are known for your accountability and reliability
• You are able to lift up to 25 kg, and are comfortable with long periods of standing and bending throughout your day
• You are able to work at least one weekend day per week

What we offer:

AbCellera’s hiring range for this role is CAD $58,800 - $74,000 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, opportunity for flexible work arrangements, 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 23353 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.

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.