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Clinical Project Coordinator - Belgium - L

Employer
ClinChoice
Location
Belgium
Salary
Competitive
Start date
5 May 2021
Closing date
3 Jun 2021

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Job Details

Description:
CROMSOURCE is recruiting for a Project Coordinator to join our Project Management team in Belgium. The role will be responsible for supporting Project Managers on assigned projects and for performing regulatory submissions, and will be 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
  • Keeps him/herself professionally abreast of all scientific, regulatory and operative aspects relevant to the clinical projects he/she will be assigned
  • 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.)
  • Collaborates with the Clinical Trial Administrators (CTAs)/Clinical Research Associates (CRAs)in terms of local authorities approval activities
  • Collaborates with the CTAs in archiving activities
  • Organizes and participates in Monitor's and Investigator's Meetings
  • Takes part in the periodic project update meetings
  • Informs PM/SPM about any issues
  • Performs, if necessary, co-monitoring visits for the assigned clinical projects
  • Carries out, after appropriate and documented training/past experiences, the monitoring of the sites for the assigned projects, when requested and if applicable
  • May acts as Feasibility Associate (FEA) after appropriate and documented 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
  • Experience in performing submissions to Ethics Committees and Competent Authorities is desirable
  • Advanced in English and local language(s)
  • Proficiency in Microsoft Office (e.g. Word, Excel, Outlook)
  • Willingness to travel


Who will you be working for?

About CROMSOURCE

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. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

Our Company Ethos

Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to 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 the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our below industry average turnover rates.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/job-information/?job-id=HQ00002548

or please contact Myna.Yeboah@cromsource.com for more information.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Keywords: Clinical Project Manager
Skills: Oncology, Clinical, clinical trials, Feasibility, GCP, ICH-GCP, Pharma, Pharmaceutical, Start-up activities Location: Belgium Share:

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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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