Associate Clinical Data Manager – FSP, GI

Fortrea

. Lead clinical data management studies involving healthy volunteer and patient populations, multi-site studies, client management, and reduced timelines .

Posted 11/12/2026full-timeRemote • CanadaMid-Level💰 CA$90,000 - CA$100,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical data management, including leadership in multi-site studies, client management, and adherence to GCP standards. Proficient in Electronic Data Capture and skilled in managing project timelines, budgets, and team performance.

Highest-signal resume keywords

Clinical Data ManagementElectronic Data CaptureSponsor ManagementProject ManagementGCP Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessData ManagementBiometricsMedical TerminologySAS ProgrammingStatisticsRisk IdentificationDatabase ReconciliationProcess ImprovementProject Productivity Metrics

Soft Skills

LeadershipMentorshipClient Relationship ManagementCommunicationProblem-Solving

Tools & Technologies

FortreaEDC DesignClinical DatabasesSafety Data SystemsLaboratory Data Systems

Industry Keywords

Standard Operating ProceduresScope of WorkClient SatisfactionCross-Functional CoordinationAudit Resolution

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead clinical data management studies involving healthy volunteer and patient populations, multi-site studies, client management, and reduced timelines
Take accountability for DM deliverables, instruct DM study teams, review outputs, and adjust resource allocations
Ensure projects comply with protocols, global harmonized SOPs, and GCP standards
Build timelines with Project Managers and coordinate with cross-functional project leads
Lead internal data-focused project meetings and coordinate EDC Design, SAS Programming, Statistics, and PK deliverables
Identify risks and mitigations, communicate data-driven discussions, and support database lock dates
Keep Project Managers, Biometrics management, sponsor services, and sponsors informed about project progress, budgets, scope changes, and timeline impacts
Develop client relationships and review client satisfaction surveys
Track scope changes and obtain Sponsor approval
Provide leadership, mentorship, and coaching in clinical trial data management processes
Support performance evaluations and career development of team members
Learn new DM technologies and applied processes and drive process improvement
Maintain accurate work records
Reconcile clinical databases against safety, laboratory, and third-party data
Represent Data Management and Biometrics in new business opportunities
Attend and action client or internal audits and resolve issues
Promote Biometrics services to sponsors

Requirements

What you’ll need

University / college degree
Relevant and equivalent experience may be considered in lieu of educational requirements
Experience and/or education plus relevant work experience equating to a bachelor's degree accepted in lieu of a bachelor's degree
Fluent in English, both written and verbal
6 to 8 years of DM experience
Minimum 1 year of direct sponsor management
Knowledge of clinical trial process, DM, clinical operations, biometrics, and system applications to support operations
Ability to adhere to project productivity metrics and timelines
Knowledge of medical terminology
3+ years of Electronic Data Capture experience preferred
Experience handling customer concerns and managing Scope of Work and budgets preferred
Knowledge of science or a scientific background preferred
Thorough knowledge of Fortrea, organizational structure, and Standard Operating Procedures preferred

Benefits

Comp & perks

Office and home-based work environment
Flexible shifts as per business requirement
Overtime and weekend work as required