Location: Padova (PD), Italy

Reports to: Tommaso Leonardi

Time: Full-time

Tutti i potenziali candidati sono invitati a leggere con attenzione i seguenti dettagli prima di inviare la propria candidatura.

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. xkiyazw The base salary shall start from 24.000 Euro per year.

Deadline for Application:

September 15th 2026

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