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Clinical Project Manager

Employer
ClinChoice
Location
Italy
Salary
Competitive
Start date
12 Feb 2019
Closing date
14 Mar 2019

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Job Details

Description:
Job Title: Project Manager

Location: Office based, Verona Italy

Schedule: Full time, 37.5 hours a week

CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. We are currently recruiting for Project Manager. We also have a number of opportunities in other therapy areas and this is a unique opportunity to become part of a rapidly growing company.

Main Job Tasks and Responsibilities
  • Manages and coordinates the assigned clinical projects
  • Manages all project specific services required by the Sponsor
  • Manages the correct development of the clinical project, interacting with the sponsor and the Investigators and properly coordinating the project team members
  • Keeps him/herself professionally abreast of all scientific, regulatory and operative aspects relevant to assigned clinical project
  • Assures the proper timelines of the assigned projects
  • Manages the budget of the project
  • Monitors the workload and the performance of the project team
  • Plans and monitors the tasks of the team in the specific areas
  • Coordinates Clinical Research Associates' (CRAs) activities
  • Collaborates with the Clinical Trial Administrators and CRAs in terms of local authorities approval activities
  • Collaborates, in the overall management of the project, with the assign Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory…)
  • Assists the Medical Monitor in preparing protocols, Case Report Forms and final Clinical Study Reports
  • Delivers project specific trainings
  • Provides project updates to the Sponsor, to the Senior Project Manager (SPM) and or Project Director/Leader
  • Performs, if necessary, co-monitoring visits for the assigned clinical projects
  • May act as Feasibility Associate (FEA) after appropriate and documented training


Education and Experience
  • University Degree in scientific, medical or paramedical disciplines
  • At least three years of Project Management experience in the CRO/Pharmaceutical industry
  • Excellent knowledge of clinical trial operations, GCP/ICH Guidelines and otherapplicable regulatory requirements
  • Advanced in English and local language(s)
  • Proficiency in Microsoft Office (e.g. Word, Excel, Outlook)
  • Willingness to travel


If you have the experience needed for this position, please apply directly to https://www.cromsource.com/careers/job-vacancies/job-information/?job-id=Hq00001356 If you would like to discuss the role before applying please contact myna.yeboah@cromsource.com for more information

Why CROMSOURCE

Our employees are the most valuable company asset and we value resources and ensure they work in a friendly, family environment and develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel clear tools to manage both internal and client processes with the same methodology.

Keywords

Project Manager,Clinical Project Manager, CPM, Study Manager, Clinical Study Manager, Budgets, ICH-GCP, Submissions, Clinical Research, CRO, Clinical Research Organisation, Clinical Trials, Clinical, Office based, Italy, Project Manager,Clinical Project Manager, CPM, Study Manager, Clinical Study Manager, Budgets, ICH-GCP, Submissions, Clinical Research, CRO, Clinical Research Organisation, Clinical Trials, Clinical, Office based, Italy
Skills: Associate Project Manager, Clinical Project Manager, Project Manager, Senior Project Manager Location: Italy

Company

ClinChoice

ClinChoice is a recognized and highly respected mid-size, global, full-service contract research organization (CRO) specializing in clinical development, post-marketing, and functional service support. We provide comprehensive end-to-end solutions, taking products from early clinical development to post-approval lifecycle management. We are committed to fostering innovation in the pharmaceutical, biotechnology, medical device & diagnostics, consumer health, cosmetics, and nutraceuticals industries. Since our establishment in 1995, we have consistently delivered high-quality services and solutions throughout the entire development lifecycle of our clients’ products. We serve a wide-ranging clientele that encompasses six of the top ten pharmaceutical companies, leading medical device companies, preeminent biotechnology companies, the largest consumer health and cosmetics companies, and numerous small-to-mid-sized innovator companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, we are positioned to fulfil our clients’ needs locally and globally.

 

We’re on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

 

Company info
Website
Telephone
+44 1628 566121
Location
Suite G48
268 Bath Road
Slough
Berkshire
SL1 4DX
United Kingdom

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