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Added 22 mins ago
NS
Human Resources Business Partner - People Services
Nova Scotia Health Authority
Yarmouth Indian Reserve No. 33, NS · Yarmouth, NS
- Full-time
Reporting to the Western Zone People Services Director and working closely with the Senior Human Resources Business Partner and western zone Employee and Labour Relations manager the HRBP…
Added 22 mins ago
WC
Manager, Maintenance - Building Services & Capital Projects (2026-323-HHS)
WoodGreen Community Services
Toronto, ON
- Full-time
The Manager, Building Services & Capital Projects, is accountable to the Senior Director, Housing Operations. The Manager of Building Services & Capital Projects is responsible for the…
Added 37 mins ago
DC
Digital Content Specialist
Diplomatic Congress of Franklin & Marshall College
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- Full-time
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Added 37 mins ago
UO
Medical Laboratory Technician Assistant Professor Educator/Program Coordinator, UC Clermont College
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Added 37 mins ago
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Added 52 mins ago
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- Full-time
Ongoing learning and career development opportunities designed to help you grow, advance, and thrive in your profession
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Winnipeg, MB · London, ON · Toronto, ON
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Added 1 hour ago
A
Senior Clinical Scientist
AbCellera
Vancouver, BC
- $120,000 to $152,000 CAD / year
We are seeking an experienced Senior Clinical Scientist to join our growing Clinical Development team, to drive early-phase development in oncology and endocrinology indications. Reporting…
Added 1 hour ago
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Added 1 hour ago
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Executive Assistant - Inclusive Education
Langley School District #35
Langley (District), BC · Langley, BC
- Full-time
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Added 1 hour ago
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Director of AI Delivery
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Added 1 hour ago
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Faculty Teaching and Learning Development Consultant
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London, ON
- Full-time
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Added 1 hour ago
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Director of AI Delivery
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Nurse Practitioner - Acute Care - Repost
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Agent(e) de soutien administratif, classe 1 - Administrative Support Agent, Class I
Champlain College Saint-Lambert
Saint-Lambert, QC · St-Lambert, QC
- $25.65 to $28.68 CAD / hour
- Full-time
Added 2 hours ago
UO
Manager, Community and Partnerships - Hunter Hub
University of Calgary
Calgary, AB
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Reporting to the Executive Director, the Manager, Community and Partnerships leads the development and delivery of community engagement, events and strategic partnership initiatives that…

AbCellera

Senior Clinical Scientist

Vancouver, BC, Canada

$120,000 to $152,000 CAD / year

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Job details

Pay: $120,000 to $152,000 CAD / year
Experience: You have 5+ years of experience in biopharmaceutical clinical development, with at least 1 year dedicated to early-phase (Phase 1–2) clinical trials
Posting language: English
Posted: Oct 26, 2026

Original job description

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 an experienced Senior Clinical Scientist to join our growing Clinical Development team, to drive early-phase development in oncology and endocrinology indications. Reporting to VP of Clinical Development and in collaboration with a Medical Director, you will integrate preclinical findings into clinical strategies and design Phase 1-2 clinical trials, author clinical study protocols and regulatory filings (INDs and CTAs) to advance novel drug candidates into clinic, execute early phase studies, and deliver proof-of-concept.

How you might spend your days

Study design and strategy: evaluating preclinical data and scientific concepts to develop clinical study Protocols, Investigator’s Brochures (IBs), Informed Consent Forms (ICFs) for Phase 1–2 dose escalation and expansion studies
Regulatory submissions: authoring clinical sections for global IND and CTA submissions, responding to inquiries from health authorities (FDA, EMA, HC), preparing protocol amendments, and contributing to Clinical Study Reports (CSRs)
Medical monitoring and patient safety oversight: supporting the Medical Director with medical monitoring and data review activities, evaluating safety, efficacy, PK and PD trends, and preparing and presenting data at Safety Monitoring Committee (SMC) meetings to drive dose decisions
Cross-functional leadership & integration: acting as the Clinical Development liaison across the organization, collaborating with:
- Translational Science: integrating preclinical scientific findings, pharmacokinetic (PK) and biomarker strategies into clinical trial design
- Biometrics and Data Management: partnering with the study statistician to develop optimal innovative study designs, contributing to data delivery, review, and interpretation to drive conclusions for proof-of-concept
- Regulatory Affairs: aligning clinical strategies with global regulatory requirements and supporting briefing document development for agency interactions
- Clinical Operations: ensuring that clinical protocols are scientifically sound and operationally feasible; providing clinical site and investigator support throughout the study cycle
- Quality Assurance: ensuring that all clinical activities and documentation strictly adhere to GCP/ICH standards and are inspection ready
External engagement: Engaging with medical experts and study investigators throughout the study cycle, contributing to advisory boards to refine clinical strategy and discuss study outcomes

We’d love to hear from you if

You have an advanced scientific degree (Ph.D., PharmD, M.S. in Life Sciences, or equivalent; MD welcomed)
You have 5+ years of experience in biopharmaceutical clinical development, with at least 1 year dedicated to early-phase (Phase 1–2) clinical trials
You have a demonstrated background in Oncology or Endocrinology/Metabolic diseases
You have knowledge of GCP, ICH guidelines, clinical trial design, medical monitoring, data review, dose-finding strategies, PK and PD assessments
You have strong problem-solving skills, able to navigate complex operational and scientific challenges

What we offer

AbCellera’s hiring range for this role is CAD $120,000 - $152,000 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 23424 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.

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More about this job

Responsibilities

The Senior Clinical Scientist will lead early-phase clinical development strategies, including designing Phase 1-2 trials and authoring regulatory filings. They will also collaborate cross-functionally to integrate preclinical findings and provide medical monitoring and safety oversight.

Requirements

Candidates must hold an advanced scientific degree such as a Ph.D., PharmD, or MD, along with at least 5 years of biopharmaceutical clinical development experience. A strong background in oncology or endocrinology and expertise in GCP/ICH guidelines are required.

Skills

Clinical trial design
Oncology
Endocrinology
Medical monitoring
Regulatory filings
Pharmacokinetics
Pharmacodynamics
GCP
ICH guidelines
Data review
Dose-finding strategies
Biomarker strategies
Protocol development
Clinical development
Translational science
Regulatory affairs

Benefits

Equity
Annual bonus
RRSP contribution
Active lifestyle allowance
Annual vacation
Professional development
Health benefits

Visa sponsorship

Not detected in the job text

Keywords

Clinical Scientist
Oncology
Endocrinology
Phase 1-2 trials
IND
CTA
GCP
ICH
Pharmacokinetics
Pharmacodynamics
Biomarkers
Regulatory Affairs
Clinical Operations
Translational Science
Biometrics
Data Management
Dose escalation
Proof-of-concept
Medical monitoring
Safety Monitoring Committee
Investigator’s Brochure
Informed Consent Form
Clinical Study Report
Biotechnology
Antibody-based medicines
Drug development
FDA
EMA
Health Canada
Clinical strategy

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