Clinical Project Manager

Vancouver - Canada

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Clinical Trials Project Manager

Clinical Project Management Team Full-time Location Remote or Hybrid. Head Office: Vancouver BC

Syreons Clinical Project Management Division is looking for a Clinical Project Manager (CPM) to join our multi-disciplinary unit in the ongoing support of cutting-edge research projects. The CPM will work cohesively with all internal departments and external clients such as Study Sponsors Monitors Investigators Site Coordinators Scientific Advisory Committee Central Ethics Boards QA and third-party vendors to facilitate a wide range of project activities.

The successful applicant will have extensive experience with the development implementation and ongoing management of research studies. The CPM is responsible for providing ongoing direction to the internal study team during all phases of the study from development to close-out.

SYREONis a full-service Contract Research Organization. We combine elite biomedical sciences advanced technologies and global clinical trial networks to speed the evaluation of new drugs diagnostics and medical devices and guide their safe effective and cost-efficient clinical use. We conduct international clinical trials and health economics and outcomes research across a broad range of chronic and rare diseases.

In this role you will:

Manage the study team to ensure all deliverables are met via project team meetings and ad hoc discussions
Be the primary point of contact for the Study Sponsor and lead study teleconferences
Develop study documents including Project Plans and Risk Management Plans
Review study documents from other departments such as CRFs Data Management Plan Data Validation Document CRF Completion Guidelines Safety Management Plan Statistical Analysis Plan Clinical Study Report
Review study protocols informed consent templates and prepares Central Ethics Boards submissions and resubmissions as required
Planning coordination and presentation at Investigators Meeting(s)
Set-up collect and maintain Trial Master Files
Set-up and distribution of Site Investigator Binders
Recruits trains and provides ongoing support to participating sites study monitors Sponsors and third-party vendors
Development and execution of Site Recruitment strategies
Review of monthly study pass-thru account statements and study budgets to ensure adherence to budget
Reviews study database and processes in collaboration with data management team as required

To be successful in this role you likely have:

BSc in life sciences or medically related field preferably OR five to eight years of industry experience within life sciences; or a minimum of five years of experience as a Clinical Research Coordinator
Excellent Clinical Research/Clinical Trials knowledge
Excellent knowledge and understanding of ICH/GCP/FDA and Health Canada Regulations
Strong written and verbal communication sills and strong presentation skills
Strong problem-solving skills
Strong ability to work in a fast-paced environment; ability to prioritize and work with speed and accuracy
Excellent competency in MS Word Excel PowerPoint analytical techniques and database applications
Excellent ability to work independently and effectively in project teams take ownership and responsibility for actions

Benefits

3 weeks of paid vacation and paid sick days
Extended health & dental
Flexible work option

Find out more:

For more information about Syreon please visit our website:

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Clinical Trials Project ManagerClinical Project Management Team Full-time Location Remote or Hybrid. Head Office: Vancouver BCSyreons Clinical Project Management Division is looking for a Clinical Project Manager (CPM) to join our multi-disciplinary unit in the ongoing support of cutting-edge res...

Clinical Trials Project Manager

Clinical Project Management Team Full-time Location Remote or Hybrid. Head Office: Vancouver BC

In this role you will:

Manage the study team to ensure all deliverables are met via project team meetings and ad hoc discussions
Be the primary point of contact for the Study Sponsor and lead study teleconferences
Develop study documents including Project Plans and Risk Management Plans
Review study documents from other departments such as CRFs Data Management Plan Data Validation Document CRF Completion Guidelines Safety Management Plan Statistical Analysis Plan Clinical Study Report
Review study protocols informed consent templates and prepares Central Ethics Boards submissions and resubmissions as required
Planning coordination and presentation at Investigators Meeting(s)
Set-up collect and maintain Trial Master Files
Set-up and distribution of Site Investigator Binders
Recruits trains and provides ongoing support to participating sites study monitors Sponsors and third-party vendors
Development and execution of Site Recruitment strategies
Review of monthly study pass-thru account statements and study budgets to ensure adherence to budget
Reviews study database and processes in collaboration with data management team as required

To be successful in this role you likely have:

BSc in life sciences or medically related field preferably OR five to eight years of industry experience within life sciences; or a minimum of five years of experience as a Clinical Research Coordinator
Excellent Clinical Research/Clinical Trials knowledge
Excellent knowledge and understanding of ICH/GCP/FDA and Health Canada Regulations
Strong written and verbal communication sills and strong presentation skills
Strong problem-solving skills
Strong ability to work in a fast-paced environment; ability to prioritize and work with speed and accuracy
Excellent competency in MS Word Excel PowerPoint analytical techniques and database applications
Excellent ability to work independently and effectively in project teams take ownership and responsibility for actions

Benefits