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Job Details

Clinical Research Associate

Company: CROMSOURCE
Location: Belgium
Reference: HQ00001140
Closing Date: 15 Feb 18
Type: Permanent
Salary (£): On Application
Benefits: Excellent and Comprehensive Benefits – see below

Job Summary:

Clinical Research Associate Location: Leuven region   Open-end contract with the client   TalentSource Life Sciences, a division of CROMSOURCE, is looking for an experienced Clinical Research Associate (CRA) to work with one of our top 10 Medical Device clients in the region of Leuven.   The Clinical Research Associate will be working with the Clinical Monitor to implement the clinical studies. Do not think this is just a regular monitoring job.

Requirements:

Clinical Research Associate

Location: Leuven region

Open-end contract with the client

TalentSource Life Sciences, a division of CROMSOURCE, is looking for an experienced Clinical Research Associate (CRA) to work with one of our top 10Medical Device clients in the region of Leuven.

The Clinical Research Associate will be working with the Clinical Monitor to implement the clinical studies. Do not think this is just a regular monitoring job. As it's a company with rather a small structure, you will be able to further expand the role, to take more responsibilities and to take a coordinating role. The term “working as a team” is very important here and everybody is being involved in the study, from Clinical Trial Assistant (CTA) to the Clinical Project Manager (CPM).

Requirements

  • Scientific background
  • Fluent in English and any other European language is an asset.
  • Minimum 3 years of experience working as a Clinical Research Associate
  • Experience in site monitoring and site management
  • Ability to problem solve
  • Good communication to successfully manage the sites
  • Establish and maintain relationships between investigational sites and internal clinical operations
  • Experience in Oncology, Cardiology and/or Peripheral Endovascular Diseases are an asset

Responsibilities

  • On-site monitoring visits
  • Follow client protocol for the SOP's and GCP
  • Participate and contribute to the study team meetings
  • Prepare the Ethic Committee submission package
  • Manage essential documents and trial supplies
  • Train site personnel
  • Solve data queries
  • Prepare and assist at audits
  • Complete all tracking systems
  • Ensure accurate and timely payments
  • Ensure timely submission of site specific documents
  • Perform close out visits

Benefits working for this client

  • Attractive salary package corresponding your education and experience
  • Being part of a top10 Medical Device company, where you can discover your own potential to make the difference
  • Working in medical devices and making a real difference in people's life

If you have the experience needed for this position, please contact Vanessa Verdickt, Consultant TalentSource Life Sciences Unit, and send your CV in Word format to vanessa.verdickt@cromsource.com.

Why TalentSource Life Sciences/CROMSOURCE

CROMSOURCE is a family-owned, high quality ISO-certified international provider of outsourced services to the pharmaceutical, biotechnology and medical device industries. Since 1994, we have been supporting our clients with outstanding clinical research and staffing solutions services. TalentSource Life Sciences is a fully dedicated flexible resourcing unit within CROMSOURCE and the successful growth 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 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.

Our approach is to equally value our clients and our own people. We know that we are not simply providing 'staff' or 'resources'. We are providing expert people. Highly talented, well trained, motivated people who make a positive difference to the work of our clients every day. Together we help our clients succeed in their work developing medicines and medical devices for patients around the world. Our large management team consists of a people with an extended experience within pharma and a high level of market knowledge. We our open, friendly and approachable and aim to support you through the recruitment process every step of the way.

As this position is client-facing, the successful candidates must be confident and be able to drive the role and themselves and to work autonomously in close liaison with a line manager at TalentSource, who will provide you with mentoring and guidance.

To ensure the success of our clients, our team of international professionals is focused on continuous improvement. We invest in our employees by providing the coaching and training necessary to deliver high quality services for our clients.

Every day we strive to create an environment in which all employees can contribute to their full potential and at the same time allow the company to develop and grow with them. With CROMSOURCE you will be able to participate in exciting projects and achieve your professional goals.

Keywords

ICH-GCP, Medical Devices, Monitoring, CRA, Clinical Research Associate, Clinical Research Coordinator, Cardiology, Oncology

Cardiology, Medical Devices, Oncology, Clinical Research Associate, Medical Device

Apply for this job: Clinical Research Associate

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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