Clinical Trial Junior Project Manager
Pubblicato il 16-09-2026 - Tommaso Leonardi - for CTNI in Torino
Location :
Padova (PD), Italy
Reports
to : Tommaso Leonardi
Time :
Full-time
Expectations for All Employees:
Supports the organization’s missions, vision and values by exhibiting the following behaviors; excellence and competence, collaboration, innovation, respect, personalization, commitment to our community, and accountability and ownership
Position Summary:
Assists with coordination of CTNI-managed clinical trials, the hire is from an EOB (Employer on Behalf)
Competencies Required:
* Excellent communication skills
* Sound interpersonal skills and the ability to supervise others
* Ability to work independently and display initiative to introduce innovations to research study
* Ability to prepare/monitor budgets
* Ability to identify problems and develop solutions
* Ability to prioritize tasks and set deadlines
Primary Duties as Junior Project Manager of a Clinical Trial:
Schedule interviews with sites
Obtain interview results from doctors, track results, and communicate results to sites and sponsors
Manage Rater Training using Excel, MGH LMS and RedCap
Manages creation of study deliverables, including SAFER Implementation Plan, Rater Training Plan, etc.
Organize and attend conference calls and distribute minutes accordingly
Attend Investigator and Sponsor Meetings as necessary
Submit study protocols, protocol amendments, and study staff certifications to the IRB
Coordinate and respond to audits by study sponsors
Other Tasks, As Required:
* Verifies accuracy of study forms
* Updates study forms per protocol
* Prepares data for analysis and data entry
* Assists with formal audits of data
* Assists with study regulatory submissions
* Verifies subject inclusion/exclusion criteria
* Maintains research data, patient files, regulatory binders and study databases
* Performs data analysis and QA/QC data checks
* May develop systems for QA/QC
* Acts as study resource for sites
* Monitors and evaluates lab and procedure data
* Prepares for FDA and IRB annual reviews