Top Tech Jobs & Startup Jobs in Montreal

Reposted 3 Days AgoSaved
Remote
Québec, QC, CAN
Mid level
Mid level
Pharmaceutical
The Clinical Operations Manager oversees trial protocols, manages budgets, ensures compliance with regulations, coordinates teams, and collaborates with vendors for clinical operations.
Reposted 5 Days AgoSaved
Remote
Québec, QC, CAN
Senior level
Senior level
Pharmaceutical
The Clinical Research Manager oversees project management and compliance for clinical trials, ensuring adherence to regulations and client policies while leading local teams to high performance.
Top Skills: Clinical Trial Management System (Ctms)Electronic Trial Master File (Etmf)Good Clinical Practice (Gcp)International Council For Harmonization (Ich)
Reposted 7 Days AgoSaved
Remote
4 Locations
Senior level
Senior level
Pharmaceutical
The Investigator Contracts Lead manages contract and budget negotiations for clinical investigator sites, overseeing contract execution and resolving related issues during studies.
Top Skills: Budgeting ProcessClinical Trial AgreementsContract NegotiationLegal Compliance
Reposted 7 Days AgoSaved
Remote
2 Locations
Senior level
Senior level
Pharmaceutical
The Investigator Contracts Lead focuses on negotiating and managing clinical trial agreements, ensuring compliance, and collaborating with various stakeholders to facilitate site contracting processes.
Top Skills: Budgeting ProcessesClinical Trial AgreementsGlobal Clinical Study Agreements
Reposted 9 Days AgoSaved
In-Office or Remote
13 Locations
Mid level
Mid level
Pharmaceutical
The operations manager oversees clinical trial activities, managing local study teams, vendor relations, and ensuring compliance with regulations while leading project tasks and addressing challenges in study execution.
Top Skills: Reporting ToolsStudy And Site Dashboards
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Reposted 9 Days AgoSaved
Remote
2 Locations
Junior
Junior
Pharmaceutical
The Site Activation Partner coordinates activities and documentation for clinical trial sites, ensuring compliance with timelines and regulations, and resolving site issues.
Top Skills: Clinical Trial SystemsFda RegulationsGCPIch
11 Days AgoSaved
In-Office or Remote
5 Locations
Mid level
Mid level
Pharmaceutical
This role involves leading CMC regulatory strategies for global product lifecycle activities, authoring documentation, and managing submissions across international markets.
Top Skills: EctdRimVeeva Vault
18 Days AgoSaved
Remote
Québec, QC, CAN
Senior level
Senior level
Pharmaceutical
The Senior Clinical Research Associate is responsible for site management, including initiation, monitoring, and closure of clinical study sites, ensuring compliance with regulations and quality standards.
Top Skills: Clinical Trial Management SystemsIch-Gcp
Reposted 19 Days AgoSaved
Remote
3 Locations
Mid level
Mid level
Pharmaceutical
Lead country-level study operations from startup through close for one or more clinical trials. Oversee local study teams and CROs, manage startup, site activation, recruitment strategies, vendor oversight, risk and issue mitigation, and ensure timely delivery of study plans and quality event follow-up.
Reposted 19 Days AgoSaved
Remote
2 Locations
Senior level
Senior level
Pharmaceutical
The Senior CRA ensures quality site management and monitoring of clinical trials, addressing protocol-related issues while maintaining compliance and investigator relations.
Top Skills: Fda RegulationsGood Clinical Practices( Gcp)
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