Job type full-time
Not provided by employer
Full job description
Psi is a leading contract research organization (cro) with more than 25 years of experience in the pharmaceutical industry.
Psi is a privately-owned, full-service globally operating croPsi’s global reach supports clinical trials across multiple countries and continents and we are known to be highly selective about the work we pursueWe focus on delivering quality and on-time services across a variety of therapeutic indications.
With an exceptionally high repeat and referral business rate combined with minimal staff turnover, psi is committed to being the best cro in the world as measured by its customers, employees, sites, and vendors.
The clinical trial lead role is a remote-based position.
As a clinical trial lead, you will have the opportunity to take on a leadership role and supervise all clinical aspects of full-service, global projectsYou will participate in the planning, implementation and management of projects in compliance with industry regulations, ich-gcp and applicable controlled documentsYou will assume responsibility for the coordination of the project team in designated countries and the monitoring of daily activities.
Manage clinical project timelines, milestones, schedules and updates during all project stages
Manage and report on key performance indicator (kpi’s); contribute to and participate in project review meetings
Ensure consistency of all study processes across regions (if delegated)
Act as primary contact for the project team, i.eCras, project assistants and psi support services
Be a point of contact for contractors and third party vendors
Manage project teams in the region, including team building, quality compliance, training and monitoring of daily activities
Contribute to the development and update of project planning documents, essential documents, and project instructions
Oversee maintenance of study-specific and corporate tracking systems
Relevant educational background, such as md, mpharm, rn or university/college degree in life sciences or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities.
Minimum 4 years’ site monitoring experience and at least 2 years’ experience as lead monitor/clinical trial lead and verified experience of supervised work in the capacity of regional lead role or equivalent.
Full working proficiency in english
Proficiency in ms office applications
Excellent communication, presentation and customer-service skills
Strong ability to negotiate and build relationships at all levels
Exceptional team-building, leadership and organizational skills
Ability to travel up to 25% (depending on project needs)
Valid driver’s license (if applicable)
All your information will be kept confidential according to eeo guidelines.
Posted 30+ days ago