Temporary
Clinical Scientist
Competitive
IT, scientific, and engineering staffing servicesScience & PharmaceuticalPosted 21d ago
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Role overview
Job type
Salary
Competitive
Sector
Posted
21 days ago
Job description
Source One Technical Solutions is recruiting for an unnamed global pharmaceutical company seeking a clinical science contractor to support clinical development and study execution, particularly early-phase oncology studies. The role contributes to protocol development, clinical data review, study planning, and cross-functional collaboration.
Responsibilities
Support clinical study strategy and design under the guidance of Clinical Science Leads and Medical Monitors
Draft and contribute to development plans, protocol profiles, clinical study protocols, informed consent forms, and clinical sections of submission documents
Review clinical data, patient profiles, data listings, and tables, listings, and graphs to support data quality and database lock
Collaborate with Clinical Operations, Biostatistics, Data Management, Translational Medicine, Clinical Pharmacology, CROs, and other study partners
Contribute to study planning, risk assessment, enrollment and retention review, protocol compliance, and clinical study report development
Conduct literature reviews and provide scientific input to clinical development activities
Preferred
an advanced degree such as a PharmD or PhD with 1–3 years of relevant experience
Phase 1–2 oncology experience
Familiarity with AI productivity tools such as ChatGPT, Microsoft Copilot, or Claude
PharmD
PhD
Relevant experience
AI productivity tools
ChatGPT
Microsoft Copilot
Claude
Benefits
100% remote or hybrid work arrangement
Company
IT, scientific, and engineering staffing services
Beachburg, Ontario, CAN
https://source1tek.com/
Founded in 1998
201-500 employees
Qualifications
Bachelor's degree with at least 3 years of relevant clinical experience
Experience supporting clinical trials and clinical study execution
Strong scientific writing, critical thinking, communication, and project coordination skills
Experience with Medidata Rave is required
Ability to work collaboratively in a deadline-driven clinical development environment
An advanced degree such as a PharmD or PhD with 1–3 years of relevant experience
Phase 1–2 oncology experience
Familiarity with AI productivity tools such as ChatGPT, Microsoft Copilot, or Claude
Bachelor’s degree with at least 3 years of relevant clinical experience
Required skills
Clinical Trial Execution, Medidata Rave, Phase 1–2 Oncology, Scientific Writing, ChatGPT, Microsoft Copilot, Claude, Project Coordination
Preferred skills
Phase 1–2 oncology experience
Experience
3+ years
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