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Associate Director, Project Management

Everest Clinical Research
Markham, CAN
Contract
Onsite
Discovered 2 weeks ago
Clinical research project managementProject planning and trackingCross-functional team leadershipClinical trials Phase I-IVBudget and resource managementProject status reporting
Free

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Key skills for this role

Clinical research project managementProject planning and trackingCross-functional team leadership
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About the Employer

Everest is a full-service contract research organization providing clinical research services to pharmaceutical, biotechnology, and medical device industries.

Everest has operated as an independent CRO since 2004 and has expertise in statistics, data management, and full-service clinical research.

Role Overview

The Associate Director, Project Management leads planning, communication, and execution of Everest clinical research and development services.

The role provides direct oversight to Project Managers and Senior Project Managers and indirect oversight to assigned Project Managers.

Workplace

  • The position is described as available at the Toronto or Markham, Ontario, Canada on-site location or remotely from a home-based office anywhere in Canada under the Work from Home policy.

Job Accountabilities

  • Train, manage, and oversee Project Managers, including performance assessments.
  • Develop governing documents, policies, and standard operating procedures for project management.
  • Plan client service delivery and coordinate cross-functional project tasks, deliverables, resources, budgets, quality, and timelines.
  • Track project progress, issue status reports, and conduct project review meetings.
  • Identify project risks and coordinate actions to support successful project starts, continuation, and completion.
  • Interact with clients regarding resource requirements and project management.
  • Manage clinical research projects involving biometrics, data management, statistics, medical writing, randomization, drug supply management, and regulatory submissions.
  • Manage Phase I-IV clinical trials in accordance with applicable regulatory and legal requirements.
  • Lead cross-functional project teams through project planning, implementation, conduct, and reporting.

Requirements

  • Experience overseeing clinical research project planning, execution, and reporting.
  • Ability to lead and manage Project Managers and Senior Project Managers.
  • Ability to manage cross-functional clinical trial projects within established budgets, timelines, quality standards, and regulatory requirements.
  • Knowledge of applicable ICH, FDA, Health Canada, EMA, and other regulatory and legal requirements.

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