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Job Details

Clinical Project Manager

Company: CROMSOURCE
Location: Argentina
Reference: HQ00001559
Closing Date: 15 Jan 19
Type: Permanent
Salary (£): On Application
Benefits: Excellent and Comprehensive Benefits – see below

Job Summary:

: Project Manager   : Argentina, Home based Schedule: Permanent     CROMSOURCE, an international, full service CRO, is looking for an experienced Project Manager to join our team, working on a large neurology study       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...

Requirements:

Job Title: Project Manager

Location: Argentina, Home based

Schedule: Permanent

CROMSOURCE, an international, full service CRO, is looking for an experienced Project Manager to join our team, working on a large neurology study

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 projects
  • 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 assigned 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 other applicable regulatory requirements
  • Experience in working on psychiatry trials is required
  • Advanced in English and local language(s)
  • Proficiency in Microsoft Office (e.g. Word, Excel, Outlook)
  • Willingness to travel

If you would like to be considered for this exciting opportunity pleased send your CV directly to holly.price@cromsource.com

CROMSOURCE is a family owned international, full-service Contract Research Organization who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

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 Project Management Clinical Trial Manager Clinical Trial Management Study Leader Study Manager Study Management PM CTM PL Project Lead Project Leader Clinical Trial Lead Clinical Trial Leader CRO Clinical Research Organisation Medical Argentina Submissions

Psychiatry, Clinical Project Manager

Apply for this job: Clinical Project Manager

Contact Information:

Address:  UK Office
CROMSOURCE Suite 3 Lomond Court Castle Business Park Stirling United Kingdom
FK9 4TU
Scotland
Tel:  +44 (0) 1786 468990
Website:  Visit Our Web Site

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