Principal Lead Data Manager at PSI CRO

Milan, Lombardy, Italy -

Full Time

Start Date

Immediate

Expiry Date

06 May, 26

Salary

0.0

Posted On

05 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Data Management, EDC Development, Data Collection, Data Cleaning, Database Lock, User Acceptance Testing, Query Management, Project Status Reporting, Data Listings, Patient Profiles, Training, Process Improvement, Audit Preparation, Team Coordination, Budget Monitoring, Timeline Management

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is a leading Contract Research Organization with more than 29 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description Acts as primary communication point for project teams and company departments regarding clinical data management. Acts as primary communication point for clients/vendors for all data management aspects of clinical projects and clinical data management reporting. Responsible for the supervision of all project data management activities of assigned studies. Coordinates data management activities within clinical projects including but not limited to EDC development, data collection, cleaning, reconciliation, Database Lock activities, development of final integrated database and generation of final Data Management deliverables. Provides input into monitoring of project scope, budget, timelines, and deliverables. Responsible for clinical data management activities including, but not limited to: development of study documentation, User acceptance testing, User access management, Data review, eCRF/External data reconciliation, SAE reconciliation, Query management, Study Database Lock activities, Archival of CRFs QC coordination, Project status reporting, Data listings/Patient profiles generation and delivery Maintains and QCs eTMF. Maintains and QCs Data Management working files. Participates in preparation for and attends internal and client/third-party audits/inspections of Data Management. Participates in follow-up on and resolution of audit findings pertaining to Data Management. Trains Lead Data Managers, Data Managers and Assistant Data Managers. Conducts project-specific training of the clinical team in CRF completion and presents at the Investigator Meetings. Provides input into proposals and assists with Business Development activities. Participates in process improvement activities at corporate/departmental level. Qualifications College or University degree or equivalent combination of training and experience that presents the required knowledge, skills, and abilities Minimum of five years of CRO industry experience as a Lead Data Manager or equivalent position At least 3 years of experience using CDM/EDC systems (Medidata Rave or Oracle Inform preferable) Project data management experience is a plus Full working proficiency in English Organizational and managerial skills Additional Information Advance your career in clinical research and develop new skillsets whilst growing with the organization.

Responsibilities

Acts as the primary communication point for project teams and clients regarding clinical data management. Responsible for supervising all project data management activities and coordinating data management activities within clinical projects.