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Associate Clinical Project Manager

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Actalent

17d ago

  • Job
    Full-time
    Junior & Mid Level
  • Research & Development
    Healthcare
  • Montréal, +1

AI generated summary

  • You need CRO or Pharma experience, Phase 1-3 trial knowledge, project management skills, timeline coordination, budget maintenance, and document preparation. In-office 2-3 days/week.
  • You will manage clinical trial activities, support project planning, track timelines, liaise with teams, maintain budgets, prepare documents, and assist in investigator meetings.

Requirements

  • CRO or Pharma experience
  • Phase 1-3 clinical trial
  • Clinical project management
  • Coordination and tracking of timelines
  • Liaison with internal functional teams
  • Collaboration with Clinical Project Managers
  • Maintaining study budget
  • Supporting document preparation and review
  • Participating in planning and conduct of investigator meetings
  • 2-3 days in office - cannot be fully remote

Responsibilities

  • - Manage clinical trial activities to ensure compliance with clinical development plans, budgets, timelines, and all applicable regulations, guidelines, quality industry standards, and internal standard operating procedures (SOPs) and policies.
  • - Support Clinical Project Managers in planning, organizing, documenting, tracking, and managing day-to-day clinical trial and regulatory activities.
  • - Coordinate and track timelines.
  • - Liaison with internal functional teams.
  • - Collaborate with Clinical Project Managers.
  • - Maintain study budget.
  • - Support document preparation and review.
  • - Participate in planning and conduct of investigator meetings.

FAQs

What is the job title for this position?

The job title is Associate Clinical Project Manager.

Where is this position located?

This position is based in Montreal, Quebec, and is a hybrid role requiring some days on-site and some days remote.

What are the primary responsibilities of the Associate Clinical Project Manager?

The Associate Clinical Project Manager will manage clinical trial activities, ensuring compliance with clinical development plans, budgets, timelines, and all applicable regulations and guidelines.

What specific phases of clinical trials does this job involve?

This role involves managing activities related to Phase 1-3 clinical trials.

What types of experience are required for this position?

Candidates should have experience in CRO or Pharma settings related to clinical project management.

What soft skills are important for this position?

Important soft skills include coordination and tracking of timelines, liaison with internal functional teams, collaboration with Clinical Project Managers, and maintaining study budgets.

Will the Associate Clinical Project Manager be involved in document preparation?

Yes, the APM will support document preparation and review as part of their responsibilities.

Is this position suitable for someone who can only work remotely?

No, this position cannot be fully remote; it requires 2-3 days in the office.

What is the work environment like for this role?

The work environment involves collaborating closely with a seasoned clinical team, requiring on-site presence for part of the week.

How does Actalent support diversity and inclusion in the workplace?

Actalent supports diversity and inclusion through hiring diverse talent, maintaining an inclusive environment, and ensuring growth opportunities for all employees.

What should I do if I need accommodations during the application process?

If you need a reasonable accommodation due to a disability, please email actalentaccommodation@actalentservices.com for assistance.

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Mission & Purpose

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