Site Activation Partner I

Pfizer

Site Activation Partner I managing clinical trial activities from initiation to close-out at Pfizer. Responsible for compliance and quality standards in clinical research operations.

Posted 7/9/2026full-timeRemote • 🇨🇦 CanadaMid-LevelSenior💰 CA$69,750 - CA$116,250 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials and site activation, ensuring compliance with regulatory standards and effective communication with stakeholders. Proficient in clinical trial methodologies, ICH-GCP, and FDA regulations, with strong technical skills to navigate multiple systems.

Highest-signal resume keywords

Clinical Trial MethodologiesICH-GCP ComplianceRegulatory Approval RequestsCross-Functional Team LeadershipBilingual Communication (French and English)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trials ManagementRegulatory Document ManagementProtocol AmendmentsStudy Lifecycle ManagementSite ActivationPharmaceutical Industry KnowledgeFDA RulesLocal RegulationsTechnical SkillsMultilingual Proficiency

Soft Skills

Strong Oral CommunicationStrong Written CommunicationCollaborationAdaptabilityProblem-Solving

Certifications & Qualifications

Bachelor’s Degree in Science/ArtsBachelor’s Degree in Life Sciences

Industry Keywords

Clinical Research OrganizationInvestigational SitesEthics Committee ApprovalsGlobal Environment ExperienceCross-Functional Teams

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead and support operational activities from initiation to close-out for assigned studies and investigational sites
Ensure adherence to deliverables, timelines, and quality standards
Manage regulatory, ethics, and essential study documents throughout the study lifecycle
Initiate and coordinate investigator site initiation kit preparation activities
Prepare and submit regulatory approval requests and collaborate with global and local Regulatory Affairs groups
Maintain ongoing communication with study teams and investigational sites
Manage document updates, including protocol amendments and ethics committee approvals

Requirements

What you’ll need

Degree/certificate or equivalent combination of education, training, and experience; bachelor’s degree in science/arts or bachelor’s degree in life sciences preferred
Minimum of 4 years’ relevant experience in a clinical trials and site activation environment
Experience in the pharmaceutical industry or with a clinical research organization is an asset
Demonstrated strong knowledge of clinical trial methodologies, ICH-GCP, FDA rules, and local regulations
Proficiency in the local language and English
Proficiency in multiple languages is an asset
Bilingualism (French and English) – the incumbent must be able to communicate effectively in English due to interaction with stakeholders and colleagues outside Quebec or Canada
Strong oral and written communication skills both internally and externally
Strong technical skills and ability to learn and use multiple systems
Experience working in a global environment
Experience working in more than one country is an asset
Experience leading or actively participating as a member of cross-functional teams and working groups

Benefits

Comp & perks

Health insurance
401(k) matching
Flexible work hours
Paid time off