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Job Details

Project Coordinator

Company: CROMSOURCE
Location: Poland
Reference: HQ00001216
Closing Date: 21 Mar 18
Type: Temporary
Salary (£): On Application
Benefits: Excellent and Comprehensive Benefits – see below

Job Summary:

Job Title: Project Coordinator   Location: Warsaw, Poland   Schedule: Full Time, 1 year FTC initially, with option to go permanent, Office Based     CROMSOURCE is urgently seeking a Project Coordinator to join our Project Management team in Warsaw. The role will be responsible for supporting Project Managers on assigned projects, working on both drug and medical device studies.

Requirements:

Job Title: Project Coordinator

Location: Warsaw, Poland

Schedule: Full Time, 1 year FTC initially, with option to go permanent, Office Based

CROMSOURCE is urgently seeking a Project Coordinator to join our Project Management team in Warsaw. The role will be responsible for supporting Project Managers on assigned projects, working on both drug and medical device studies.

Main Job Tasks and Responsibilities

  • Manages and coordinates the assigned clinical projects under the supervision of the Project Manager (PM)/ Senior Project Manager (SPM)
  • Manages all project specific services required by the Sponsor (centralized lab exams, drug shipments, documents shipment, etc.)
  • Manages the correct development of the clinical project, interacting with the Sponsor and the Investigators under the supervision of the PM/SPM
  • Should be knowledgeable, following appropriate trainings, in the application process for clinical studies, in force in the country(ies) of work. Accordingly he/she can be required to provide updates on the topic, whenever relevant
  • Collects and manages study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)
  • Coordinates the activities of Clinical Research Associates, ensuring the compliance with the ICH/GCP guidelines and applicable laws and regulations
  • Collaborates with the Clinical Trial Administrators/Clinical Research Associates
  • Takes part in the periodic project update meetings
  • Informs PM/SPM about any issues
  • May act as Third Party Vendor (TPV) Specialist responsible for TPV managing all project specific services required by the Sponsor (centralized lab exams, drug shipments, documents shipment etc.)
  • May act as Technical Specialist supervising the projects within specific therapeutic/technical areas under the supervision of the PM and only after appropriate training

Education and Experience

  • University Degree in scientific, medical or paramedical disciplines
  • Previous experience in the clinical research industry, in either a CRA or project coordination function
  • Excellent knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory requirements
  • 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 myna.yeboah@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 Coordinator Project Assistant Junior Project Manager Clinical Trial Coordinator Clinical Research Coordinator Warsaw Warszawa Poland Clinical Operations

Project Co-ordinator

Apply for this job: Project Coordinator

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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