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Job Description & How to Apply Below
About the Role
We are seeking a Clinical Scientist 2, Clinical Development to join our Clinical Development team. This role is intended for an experienced clinical scientist who can independently contribute to the design, execution, analysis, interpretation, and communication of clinical development activities across assigned programs. The clinical scientist will provide scientific leadership at the study level, contribute meaningfully to program strategy, and serve as a key partner to cross‑functional teams to ensure that clinical development plans, study designs, and data packages are scientifically rigorous, operationally feasible, and aligned with evolving regulatory expectations.
This position reports to the Senior Medical Director, Clinical Development, and will be based out of our Vancouver, BC office. We may consider remote locations for exceptional candidates. This is a hybrid position requiring a minimum of two onsite days per week.
Duties and Responsibilities
Provide scientific leadership and independent contribution to study design, protocol development, endpoint strategy, and clinical development planning for assigned programs.
Support the development, implementation, conduct, oversight, and reporting of clinical trials, ensuring scientific quality and alignment with program objectives.
Perform comprehensive literature reviews and maintain current knowledge of disease areas, competitive landscape, emerging science, and regulatory developments relevant to assigned products and indications.
Participate in review, monitoring, summarization, and interpretation of safety, efficacy, pharmacokinetic, patient‑reported outcome, and other clinical data to support development decisions and recommendations.
Collaborate cross‑functionally with Clinical Operations, Biometrics/Biostatistics, Data Management, Pharmacovigilance, Medical Writing, Regulatory, Translational Development, Medical Affairs, and other partners to support high‑quality study execution and documentation.
Draft, review, and contribute to clinical and regulatory documents, including study protocols, synopses, investigator brochures, clinical study reports, health authority submission content, briefing materials, abstracts, posters, and manuscripts.
Support or lead scientific interactions with CROs, investigators, site personnel, and external collaborators to ensure consistency, scientific integrity, and effective study execution.
Contribute to investigator identification, site feasibility, study start‑up, and scientific training activities for study teams, CROs, investigators, and site personnel.
Develop and maintain productive relationships with external scientific experts, key opinion leaders, and the broader medical community in alignment with development goals.
Provide critical evaluation of development strategies, identify scientific and operational risks, and help develop contingency and mitigation plans.
Contribute to advisory boards, expert meetings, and other scientific interactions that support program development and evidence generation.
Support the development of departmental processes, templates, standard operating procedures, and best practices as needed.
Develop SOPs and guidelines linked with departmental activities.
Act in accordance with Company policies, including the Code of Business Conduct and Ethics and ensure policies are understood and followed by direct reports, if any.
Other Duties
Other duties as assigned.
Qualifications
MSc or PhD degree in Life Sciences, Biomedical Sciences, Pharmacology or other professional doctorate in pharmaceutical sciences or a related scientific discipline.
At least 2-5 years of post‑doctoral experience and/or relevant industry experience, preferably in neurosciences.
Experience in clinical research and clinical development with a strong understanding of study design, study conduct, clinical data review, and interpretation.
Experience drafting, reviewing, or supporting clinical and regulatory documentation and working effectively in cross‑functional teams.
Working knowledge of GCP, ICH guidelines, and regulatory expectations, including familiarity with FDA and EMA environments.
Strong…
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