Clinical Trial Junior Project Manager

Location: Padova (PD), Italy

Le informazioni riportate di seguito illustrano i requisiti del ruolo, l'esperienza richiesta ai candidati e le qualifiche associate. 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 Recommends protocol changes and may assist with writing protocols and manuscripts Works with PI to prepare complete study reports Responsible for quality control Designs research protocols in conjunction with PI Assists in the selection of study sites Tracks and analyzes trends across studies, study sites, and CTNI clinicians Invoices sponsors and processes payments to vendors Orders supplies, handles computer and telephone issues, and communicates with property management Participates in regular meetings with operations and clinical teams Facilitates any rater communication with study sites as requested Creates/distributes study reminders Acts as general resource for study information Requirements: Bachelor degree required. Appreciated a 1-3 years of work experience/clinical experience Must be knowledgeable about computers and data management systems and familiar with common software packages (Word, Excel, PowerPoint, Access, Outlook) and Internet communication Familiarity with statistical packages (SPSS, SAS) desirable Must have the capability of prioritizing multiple competing tasks and seek supervisory or administrative assistance when appropriate Work Schedule (flexible): Monday through Friday, 9:00 to 18:30 or 18 (depending on lunch break choice) Working Relationships: Must be able to communicate in English well both verbally and in writing with internal and external clients Salary: negotiable RAL, spending on experience and previous qualifications. xpavfwm The base salary shall start from 24.000 Euro per year. Deadline for Application: September 15th 2026