Clinical Project Manager
Syreon Corporation
full-time
Posted on:
Location Type: Hybrid
Location: Vancouver • 🇨🇦 Canada
Visit company websiteJob Level
Mid-LevelSenior
Tech Stack
Google Cloud Platform
About the role
- 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 Investigator’s 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
Requirements
- 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 skills, 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
Clinical ResearchClinical TrialsProject PlansRisk Management PlansData Management PlanStatistical Analysis PlanTrial Master FilesSite Recruitment strategiesBudget adherenceAnalytical techniques
Soft skills
Communication skillsPresentation skillsProblem-solving skillsAbility to prioritizeAbility to work independentlyTeamworkOwnershipResponsibilityAdaptabilityAttention to detail