Associate Project Manager

Canada
Remote
Posted Oct 15, 2026
1 position

$70–$80 / hour

Opens an external site

Employment type: Full-time
Experience level: Entry, Junior · 0+ years
Minimum education: Professional degree
Posting language: English
Working hours: 40 hours per week

Job summary

The Associate Project Manager will support the planning, coordination, and delivery of clinical research and biometrics projects by monitoring timelines, budgets, and quality standards. They will collaborate with cross-functional teams to track deliverables, manage risks, and ensure adherence to regulatory requirements.

Job details

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for an Associate Project Manager based in Canada. As an Associate Project Manager, you will support the planning, coordination, and delivery of clinical research and biometrics projects within the pharmaceutical and life sciences industry. You will work closely with cross-functional teams, including Biostatistics, Statistical Programming, and Data Management, to ensure projects progress efficiently and meet established milestones. Your role will contribute to the successful execution of clinical trials by monitoring timelines, deliverables, resources, budgets, and quality standards. You will collaborate with project managers, functional leads, and clients to maintain clear communication, track progress, and address potential risks. This opportunity is ideal for an early-career professional looking to develop project management expertise in a highly regulated, quality-focused environment. You will gain exposure to clinical development processes, project financial management, and international collaboration while helping advance the delivery of innovative medicines and medical technologies. Join a collaborative and inclusive team where continuous learning, professional development, and meaningful contributions to global healthcare are encouraged. \n Accountabilities Project planning and delivery: Support the development and maintenance of project plans, timelines, milestones, deliverables, and resource requirements. Coordinate biometrics activities across Biostatistics, Statistical Programming, and Data Management, and monitor progress against agreed project scope and deadlines. Cross-functional coordination: Follow up with functional leads and project team members on deliverables, dependencies, and outstanding actions. Assist with coordinating multiple studies or workstreams and support critical milestones, including database lock, statistical analysis, and reporting. Client and team communication: Participate in client and internal project meetings, prepare agendas and status updates, document meeting minutes, and maintain action-item trackers. Facilitate routine meetings as experience develops and ensure effective communication between clients, project managers, and functional teams. Risk and issue management: Maintain project risk, issue, decision, and action logs. Identify potential delays, resource constraints, scope changes, and delivery risks, and support the development and monitoring of mitigation and recovery plans. Escalate issues to the appropriate project manager or functional leader when necessary. Scope and financial management: Assist with tracking project budgets, hours, milestones, forecasts, and financial performance. Monitor activities against contracted scopes of work, identify potential out-of-scope requests, and contribute to change-order documentation and financial updates. Quality and regulatory compliance: Support project delivery in accordance with applicable standard operating procedures (SOPs), contractual obligations, client requirements, and quality standards. Maintain accurate project documentation and trackers, coordinate the resolution of quality issues, and contribute to inspection and audit readiness. Continuous improvement: Work collaboratively with project managers and functional teams to improve project coordination, documentation practices, and delivery processes while developing your project management capabilities. Requirements Education: A bachelor's degree or higher in life sciences is required. An MBA or Project Management Professional (PMP) certification is considered an asset. Professional experience: Between 0 and 2 years of relevant experience in the pharmaceutical, biotechnology, or Contract Research Organization (CRO) industry. Previous experience in project coordination, clinical operations, Data Management, Biostatistics, Statistical Programming, or another biometrics-related function is an advantage. Clinical research knowledge: A basic understanding of clinical drug development and clinical trial processes, with familiarity with applicable regulatory requirements, FDA regulations, and ICH Good Clinical Practice (GCP) guidelines. Project management fundamentals: Familiarity with core project management concepts, including scope, timelines, budgets, milestones, dependencies, risk management, and change control. Organizational skills: Strong planning, prioritization, and time-management abilities, with excellent attention to detail and consistent follow-through on assigned tasks. Communication skills: Strong written and verbal communication skills, including the ability to prepare clear project documentation, meeting notes, status reports, and professional correspondence. Teamwork and client focus: Excellent interpersonal skills, a collaborative mindset, and a customer-focused approach to working with colleagues, project managers, functional specialists, and clients. Technical proficiency: Proficiency in Microsoft Office applications, particularly Word, Excel, PowerPoint, and Outlook. Familiarity with Microsoft Project is also required. Adaptability and learning: A proactive attitude, willingness to learn, and ability to work effectively in a structured, quality-driven environment while managing multiple priorities. Commitment to quality and inclusion: An appreciation for accuracy, regulatory compliance, continuous improvement, and respectful collaboration within diverse teams. Benefits Competitive compensation: An advertised Canadian pay range of CAD $70–$80 per hour. The final rate may vary depending on qualifications, skills, competencies, and relevant experience. Remote work opportunity: A remote position offering the flexibility to work from Canada. Professional development: The opportunity to build project management experience in clinical research and develop expertise across biometrics, clinical development, and regulated project delivery. Continuous learning: Exposure to established project management processes, quality standards, and clinical research practices, with opportunities to strengthen professional skills. Meaningful impact: Contribute to the development and commercialization of innovative medicines and medical devices that support global health and patient safety. Collaborative environment: Work with multidisciplinary teams and professionals across clinical research and related functions. Inclusive workplace: Join an organization that values diversity, equal opportunity, and a respectful working environment. Accessibility support: Reasonable accommodations are available to qualified applicants throughout the recruitment and selection process upon request. \n How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1

What you’ll do

Requirements

Candidates must hold a bachelor's degree in life sciences and possess 0 to 2 years of relevant experience in the pharmaceutical or CRO industry. Strong organizational skills, proficiency in Microsoft Office and Microsoft Project, and a basic understanding of clinical trial processes are required.