pstrongLocation /strong: Padova (PD), Italy /ppstrongReports /strong strongto /strong: Tommaso Leonardi /ppstrongTime /strong: Full-time /ppbr / /ppstrongExpectations for All Employees: /strong /ppSupports 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 /ppbr / /ppstrongPosition Summary: /strong /ppAssists with coordination of CTNI-managed clinical trials, the hire is from an EOB (Employer on Behalf) /ppbr / /ppstrongCompetencies Required: /strong /pp * Excellent communication skills /pp * Sound interpersonal skills and the ability to supervise others /pp * Ability to work independently and display initiative to introduce innovations to research study /pp * Ability to prepare/monitor budgets /pp * Ability to identify problems and develop solutions /pp * Ability to prioritize tasks and set deadlines /ppbr / /ppstrongPrimary Duties as Junior Project Manager of a Clinical Trial: /strong /polliSchedule interviews with sites /liliObtain interview results from doctors, track results, and communicate results to sites and sponsors /liliManage Rater Training using Excel, MGH LMS and RedCap /liliManages creation of study deliverables, including SAFER Implementation Plan, Rater Training Plan, etc. /liliOrganize and attend conference calls and distribute minutes accordingly /liliAttend Investigator and Sponsor Meetings as necessary /liliSubmit study protocols, protocol amendments, and study staff certifications to the IRB /liliCoordinate and respond to audits by study sponsors /li /olpbr / /ppstrongOther Tasks, As Required: /strong /pp * Verifies accuracy of study forms /pp * Updates study forms per protocol /pp * Prepares data for analysis and data entry /pp * Assists with formal audits of data /pp * Assists with study regulatory submissions /pp * Verifies subject inclusion/exclusion criteria /pp * Maintains research data, patient files,



regulatory binders and study databases /pp * Performs data analysis and QA/QC data checks /pp * May develop systems for QA/QC /pp * Acts as study resource for sites /pp * Monitors and evaluates lab and procedure data /pp * Prepares for FDA and IRB annual reviews /pp * Recommends protocol changes and may assist with writing protocols and manuscripts /pp * Works with PI to prepare complete study reports /pp * Responsible for quality control /pp * Designs research protocols in conjunction with PI /pp strong* /strongAssists in the selection of study sites /pp * Tracks and analyzes trends across studies, study sites, and CTNI clinicians /pp * Invoices sponsors and processes payments to vendors /pp * Orders supplies, handles computer and telephone issues, and communicates with property management /pp * Participates in regular meetings with operations and clinical teams /pp * Facilitates any rater communication with study sites as requested /pp * Creates/distributes study reminders /pp * Acts as general resource for study information /ppbr / /ppstrongRequirements: /strong /ppBachelor degree required. /ppAppreciated a 1-3 years of work experience/clinical experience /ppMust be knowledgeable about computers and data management systems and familiar with common software packages (Word, Excel, PowerPoint, Access, Outlook) and Internet communication /ppFamiliarity with statistical packages (SPSS, SAS) desirable /ppMust have the capability of prioritizing multiple competing tasks and seek supervisory or administrative assistance when appropriate /ppbr / /ppstrongWork Schedule (flexible): /strong /ppMonday through Friday, 9:00 to 18:30 or 18 (depending on lunch break choice) /ppbr / /ppstrongWorking Relationships: /strong /ppMust be able to communicate in English well both verbally and in writing with internal and external clients /ppbr / /ppstrongSalary /strong: negotiable RAL, spending on experience and previous qualifications. The base salary shall start from 24.000 Euro per year. /ppstrongDeadline for Application: /strong /ppstrongSeptember 15th 2026 /strong /p

📌 Clinical Trial Junior Project Manager (Padova)
🏢 Tommaso Leonardi - for CTNI
📍 Padova