Clinical Trial Lead

2 giorni fa


Milano, Italia Meet Recruitment A tempo pieno

Competitive
- Milan, Italy
- Permanent

We are looking for a Clinical Trial Lead to join our Clinical Operations team where you will be responsible for managing the planning, implementation, and tracking of the clinical monitoring process. You will maintain an overview of ongoing tasks within the Clinical Operations department and acts as a guide to Clinical Research Associates and In-House Clinical Research Associate activities.

You will work closely with Project Management, Business Development and the Sponsor and will play a significant role in ensuring that deadlines of projects are met in accordance with contracted scope of work, budgeted hours whilst ensuring maximum efficiency and quality.

**KEY ACCOUNTABILITIES**
- Responsible for oversight of CRA and IHCRA activity on the assigned study.
- Responsible for the Preparation, maintenance and execution of Clinical Operations plans.
- Ensures study team receives study specific training according to Simbec-Orion SOPs.
- Ensures all monitoring tasks are delivered on time and within agreed monitoring budget.
- Communicates progress and assist Project Manager with tracking of project status.
- Assist Project Manager with budgeting throughout the project and forecasting of URFs.
- Contributes to regular updates to Clinical Trial Systems.
- Act as a CRA on the project, where necessary.

**SKILLS REQUIRED**

**Essential**
- _Bachelor’s degree in Nursing, Life Sciences or Medical Sciences _
- or equivalent work experience required_
- _Experience as a Clinical Research Associate III_
- _Excellent communication skills_
- _Proficiency in written and spoken English; fluent in host country language_
- _Expert knowledge of relevant clinical research regulations and ICH-GCP_
- _Ability to establish/maintain good relationships with sites/colleagues/clients_
- _Ability to make decisions independently / Strong problem-solving skills_
- _Highly developed mentoring and motivational skills_

**Desirable**
- _Previous CRO experience_
- _Good experience in CTMS, eTMF IXRS and EDC systems_
- _Advanced degree (Masters, MD, PhD)_
- _Strong presentation skills_
- _Competent in clinical trial planning and metrics management_
- _Multiple therapeutic experience and proven ability to gain in-depth protocol knowledge_



  • Milano, Italia Syneos Health Clinical A tempo pieno

    **Overview** The Clinical Trial Ambassador will establish, cultivate, and maintain scientific relationships with investigators and study coordinators to support enrollment while developing a strong understanding of clinical practice as it relates to areas of interest. This position interacts with various internal and external stakeholders, with a focus on...


  • Milano, Italia Syneos Health Clinical A tempo pieno

    **Overview**The Clinical Trial Ambassador will establish, cultivate, and maintain scientific relationships with investigators and study coordinators to support enrollment while developing a strong understanding of clinical practice as it relates to areas of interest.This position interacts with various internal and external stakeholders, with a focus on...


  • Milano, Italia Thermo Fisher Scientific A tempo pieno

    **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office The Clinical Trial Manager (CTM) operates cross-functionally with global accountability for operational deliverables of clinical studies from Final Protocol Concept Sheet to Clinical Study Report (CSR) and applicable results disclosure. The CTM provides operational expertise and...


  • Milano, Italia IQVIA A tempo pieno

    On behalf of our Client a global pharmaceutical company, IQVIA is looking for a **Clinical Trial Supply Coordinator** who can join an exciting working environment in a dynamic atmosphere. **RESPONSIBILITIES**: The CTS Coordinator acts in a complex and international environment. - Develop packaging design solutions for clinical trial materials tailored for...

  • Clinical Trial Director

    2 settimane fa


    Milano, Lombardia, Italia Bancroft School A tempo pieno

    Clinical Trial Director Job DescriptionBancroft School is a leading provider of educational services and is seeking a highly skilled Clinical Trial Director to join our team. As a Clinical Trial Director, you will be responsible for managing the day-to-day operations of clinical trials and ensuring compliance with regulatory...


  • Milano, Italia Iqvia A tempo pieno

    On behalf of our Client a global pharmaceutical company, IQVIA is looking for a **Clinical Trial Supply Coordinator** who can join an exciting working environment in a dynamic atmosphere.**RESPONSIBILITIES**:The CTS Coordinator acts in a complex and international environment.- Develop packaging design solutions for clinical trial materials tailored for...


  • Milano, Italia BI Italia Spa A tempo pieno

    **THE POSITION**: The Junior Clinical Trial Manager (JCTM) is a key position in local on the delivery of Boehringer Ingelheim’s pipeline and accountable for the operational and scientific oversight, the set-up, execution and delivery of their assigned clinical trials at local level. **For this position we offer a one year fixed term contract with external...


  • Milano, Lombardia, Italia Mil Fortrea Clinical Development Ltd Filiale Italiana A tempo pieno

    Job OverviewAt Mil Fortrea Clinical Development Ltd Filiale Italiana, we are seeking a skilled Clinical Trial Operations Manager to oversee local deliverables and ensure seamless execution of clinical trials. This role is ideal for individuals with a passion for scientific rigor and experience in managing country-specific trial commitments.About the RoleThis...


  • Milano, Italia Novartis A tempo pieno

    100,000+ That’s how many patients participate in our clinical trials at any given time. GCO (Global Clinical Operations) is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link...


  • Milano, Italia Novartis A tempo pieno

    100,000+ That's how many patients participate in our clinical trials at any given time. GCO (Global Clinical Operations) is Novartis' powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between...


  • Milano, Italia CTI Clinical Trial Services, Inc A tempo pieno

    **Clinical Project Assistant / Coordinator for our Italian Team** **Job Purpose/Summary** - Responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, and quality standards are being achieved. **What You’ll Do** - Support Clinical Project Manager / Director in completing management activities; supports...


  • Milano, Italia JSB SOLUTIONS S.R.L A tempo pieno

    **JSB Solutions**, azienda di consulenza nata nel 2009 con 3 sedi in Italia (Firenze, Parma e Milano) è alla ricerca di un **Clinical Trial Manager**: - (JSB.SRF.22.093)_ da inserire nel nostro team di consulenti in area **CRO **per la nostra sede di **Milano**. **Clinical Project Management di almeno 3 anni in contesti farmaceutici** e sarà inserito...


  • Milano, Italia IQVIA A tempo pieno

    Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and...


  • Milano, Italia Icon plc A tempo pieno

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. - With our patients at the centre of all that we do, we help to accelerate the...


  • Milano, Italia IQVIA A tempo pieno

    **Clinical Trials Assistant - Multisponsor - Milano (Hybrid)** Job Overview: Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions: - Assist Clinical Research Associates (CRAs) and Regulatory and...


  • Milano, Italia Iqvia A tempo pieno

    Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and...


  • Milano, Italia Novasyte A tempo pieno

    Job Overview CTEs collaborate with research staff and other stakeholders to drive trial recruitment and to support study specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimise the site experience and performance. Leads the relationship management and communication of medical and scientific...


  • Milano, Italia Novasyte A tempo pieno

    Internal Job Description - Clinical Trial Administrator, Single Sponsor dedicatedJob Overview: - CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. By assisting in the coordination and administration of the study...

  • Clinical Trial Assistant

    2 settimane fa


    Milano, Italia Iqvia A tempo pieno

    **Clinical Trials Assistant - Multisponsor - Milano (Hybrid)**Job Overview:Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions:- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up...


  • Milano, Italia Novasyte A tempo pieno

    Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and...