Project Specialist - Toronto, Canada - Allucent

Allucent
Allucent
Verified Company
Toronto, Canada

2 weeks ago

Sophia Lee

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Sophia Lee

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Description

These customers have new therapeutic ideas, but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities.

You'll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you'll help make a positive difference in patients' lives.


Summary:


We currently looking for an experienced Project Specialist I and II to join our team in Canada, Brazil, or the UK The Project Specialist (PS) provides support to project management to deliver projects within the established budget and timeline.

Typical duties include coordination of project activities through collaboration with project team members, dissemination of project information and guidance to ensure adequate support for the study team, preparation of agendas for meetings, documenting key decisions and providing relevant updates as needed.

In general, PS I and PS II have equivalent skill sets and responsibilities.

The main factor which differentiates PS I from PS II is a level of knowledge, and, consequently, level of required supervision and decision-making ability.


Location:
Canada, Brazil, or the UK


Experience: 3+ years in Clinical Research


Workplace options:
Hybrid/Remote/On-site


Language:
excellent professional level of English required


The Project Specialist is responsible for the following tasks:
Project team continuous support includes, but is not limited to work with the PM and the project team and assist with the tasks, including:

  • Create and/or maintain tracking tools for clinical data management
  • Enter data into systems and tools per required processes
  • Review reports in applicable systems to ensure completeness, consistency and information is up to date prior to their distribution
  • Coordinate, prepare, handle, and distribute clinical trial support materials if done centrally
  • Support with the preparation of the studyrelated presentation materials (Kick off Meeting, CRA Training and Investigator Meeting, regular and ad hoc meetings) and present as needed
  • Support in creation of Project Plan and other study plans including associated templates
  • Attend handover meetings for the CTAs who are joining/leaving the study and review handover form
  • Support PMs during audits/inspections. Ensure followup on open action item for resolution within given timelines
  • Assist PM with vendor management, as needed
  • Support Clients with ad hoc requests
  • Within the scope of assigned responsibilities resolve study related problems, and offer action plans

Communication:

  • Facilitate team communication and liaise with sponsors, sites and third parties
  • Prepare Study Correspondence Management Plan (SCMP)
  • Process Public Folders (PF) for study level as per SCMP Ensure study PFs are maintained by the trial team to accomplish inspection readiness
  • Coordinate internal and external project team conference calls, process agendas, meeting minutes, and action log or equivalent

Filing:

  • Adapt default folders on SharePoint
  • Support TMF Lead (TMFL) with the setup of Trial Master File (TMF)
  • As a document owner, is responsible for document filing on trial level, and can act as a document submitter for other document owners on trial level as needed
  • Work with TMFL on reconciliation of TMF trial level documents
  • Coordinate and support the project team with the periodic review of study files for accuracy, quality, and completeness, including tracking of the outstanding issues for proper resolution
  • Coordinate and support the project team with the final reconciliation and offsite archival of project documentation
  • Provide clear guidance to CRAs / CTAs and coordinate setup of investigator site files
  • Customize and distribute study logs/forms/templates

Other:

  • With the PM, ensure all activities included in the project scope of work are completed and project timelines are met
  • If delegated by PM/CTL, enter trial level data in CTMS and conduct monthly reviews to ensure that content is accurate and up to date. Follow up with local study teams to ensure country and site level data is being updated regularly in CTMS
  • Support PMs with budget related activities, as needed
  • Create Contracted FTE by Month files
  • Administrative support for Trial Committees activities for assigned studies

Requirements:


Qualifications:


  • Life science, healthcare and/or business degree preferred. High School Diploma/Certificate or equivalent combination of education, training and experience required
  • Minimum 2 years of relevant work experience in similar positions
  • Minimum 4 years of experience in drug development and/or clinical research
  • Basic knowledge of GxP
  • GDPR and applicable regulatory requirements

Skills

  • Strong written and verbal communication skills including good command of English language
  • Representative, outgoing and client focused
  • Ability to work in a fastpaced challenging environment of a
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