On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Clinical Project Manager (fixed-term maternity cover). Scopra esattamente quali competenze, esperienze e qualifiche sono necessarie per avere successo in questo ruolo prima di candidarsi.
Responsibilities
* Makes operational decisions to ensure that projects are initiated and completed on time, on budget and to the required quality standards, secures compliance with ICH and Chiesi Standard Operating Procedures (SOPs) or any local regulations.
* Can be involved in the writing/review of SOPs and working instructions (WI) and completes assigned SOPs/WIs/processes trainings according to company process.
* Develops full synopsis and protocol, and related documents based on the Study Outline contained in the Clinical Development Plan (CDP) involving all relevant contributors.
* Collaborates with relevant contributors and accountable team members to ensure timely production and review of other important study‑related documents.
* Contributes to the CRO and/or Providers selection: responsible for the implementation of the Request For Proposal (RFP), reviews and assesses proposals, reviews scope of works and overall budget.
* Responsible for management of the Clinical CRO/Providers acting as primary contact for Clinical CRO but also internal customers, ensuring adherence to scope of work within timelines and budget.
* Performs co‑monitoring when needed, as specified in SOP, and collaborates with Site Engagement Managers for study site performance and relationship consolidation.
* Collaborates in the set‑up and maintenance of the Study Risk Register and is responsible for ongoing clinical risk review during study conduct involving all relevant study team functions and for the follow‑up on actions with vendors (CRO, direct and third‑party vendors).
* Prepares and coordinates scientific meetings: investigators’ meeting, scientific/safety board meetings, data reviews and any other study‑relevant meetings.
* Ensures registration of the study in public registries (e.g., European registry).
* liaises with Clinical Trial Supply (CTS) coordinator to define the CTS strategy/plan, reviews the labels and leaflets.
* Responsible for the management of the study eTMF (related to clinical operations) and all its related activities (such as QC and health checks) with the Clinical Trial Administrator (CTA) as per Chiesi SOP.
* Accountable for overall completeness of the whole study eTMF and for ensuring that the study eTMF is archived as per Chiesi SOP.
* Accountable for budget management and reconciliation as well as control of invoices on a monthly basis; twice a year provides forecast & pre‑closing budgets according to study progress.
* Coordinates the preparation of the Clinical Study Report (CSR) in cooperation with the Medical Writer, reviews the CSR/CIR, and coordinates its review/approval by required members; reviews layman summaries and study summaries for authorities.
* Supports and/or coordinates the presentation of clinical study results internally and externally and the preparation of manuscripts for full paper publication.
Qualifications
* Degree in Life Sciences or equivalent.
* At least 2–3 years of experience in Project Management or as a Clinical Research Associate (CRA).
* Track record of achievements in successful planning and execution of at least 5 clinical studies.
* Added value for direct experience in implementation of centralized systems set up and large clinical trial experience in respiratory therapeutic area.
* Planning & Organizing.
* Problem Solving.
* Results Driven.
* Priority Setting.
* Fluent English.
Contract Details
Fixed Term – temporary position covering maternity leave.
Please enter the authorization for the processing of personal data (DL196/2003) – General Data Protection Regulation (13 GDPR 679/16) to IQVIA and to transfer those data to IQVIA’s Clients.
The research is urgent and is intended for candidates of both sexes (L.903/77).
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