Leading cross-functional teams and third parties/vendors to ensure successful project delivery. Overseeing clinical research conduct, including study start-up, enrollment, execution, and close-out
Acting as liaison with the client and managing client contractual, organizational and relationship needs/expectations, related to operational delivery of assigned projects
Managing project contractual deliverables and modifications, and preparing and delivering study-related updates, dashboards and reports to study teams, senior management, and sponsors / vendors / partners, including but not limited to: Recruitment, screening, and enrollment reports
Ensuring project management systems are updated weekly to reflect accurate project status
Serving as a point of escalation for project team members
Participating in revenue forecasting and review of project actual unit/hours efficiency against budget
Organizing and leading study team meetings, and meetings with sponsors / vendors / partners as applicable
Requirements
Undergraduate, health-related degree OR an equivalent combination of education, training, and experience sufficient to successfully perform the key responsibilities of the job
5+ years of relevant clinical research experience and solid knowledge and understanding of clinical project / trial management
Experience working in a CRO, Site, SMO or Sponsor preferred
Benefits
Top notch healthcare (medical, dental, and vision) for you and your family.
A 100% 401(k) company match for up to 4% of eligible contributions with an immediate vesting.
Company provided laptop, your choice of a PC or a Mac
Monthly stipend for internet and phone expenses
Short & long-term disability
Life insurance and More!
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.