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Job Details

Clinical Data Associate

Company: CROMSOURCE
Location: Belgium
Reference: HQ00001205
Closing Date: 21 Mar 18
Type: Permanent
Salary (£): On Application
Benefits: Excellent and Comprehensive Benefits – see below

Job Summary:

Clinical Data AssociateLeuven regionPermanent placement TalentSource Life Sciences, a division of CROMSOURCE, dedicated to flexible staffing solutions, is urgently currently seeking a motivated and talented Clinical Data Associate, to strengthen our team at one of our clients, a leading Medical Device company located in Leuven, Belgium. Stepping into this opportunity will make your part of the medical devices industry, where you are able to make a visible difference in...

Requirements:

Clinical Data Associate
Leuven region
Permanent placement

TalentSource Life Sciences, a division of CROMSOURCE, dedicated to flexible staffing solutions, is urgently currently seeking a motivated and talented Clinical Data Associate, to strengthen our team at one of our clients, a leading Medical Device company located in Leuven, Belgium. Stepping into this opportunity will make your part of the medical devices industry, where you are able to make a visible difference in people's lives. Join us and discover your own potential to make that difference.

Mission Description

The objectives of the European Medical and Clinical Division are to organize, manage and conduct clinical trials by respecting all regulatory requirements and Good Clinical practice, to communicate clinical data to wider audience, to manage all medical aspects of company products, and to contribute to the new products and new therapies development.

Key Responsibilities

Clinical data management

- Performs ongoing data cleaning and reviews to assure quality of the data and compliance with Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and ICH Guidelines

- Partner with clinical operations personnel to manage the query lifecycle

- Assist in eCRF development

- Edit checks and UAT of clinical studies

- Creates and delivers study-specific site training

- Responsible for handling all pre and post production service requests

- Assist Program Data Manager while developing and maintaining data management processes in compliance with Standard Operating Procedures (SOP)

Preparation and conduct of Clinical Trials

- Ensure accuracy of clinical data through review of CRFs for completeness and consistency

- Provide clinical data export or reports to clinical operations team

- Partner with external service providers to support department goals

Regulatory issues

- Closely follow the regulations related to conduct of clinical trials in different countries

- Assist in updating DM processes to any change in regulation

- Assist in SOP preparation and update

Profile Required

- Master's degree in Bio-medical / Pharma / Life science or Bachelor's Informatics

- Professional experience of about 1-3 years in data management for clinical trial$

- Experience in Medical devices (Oncology, Cardiology) is an advantage

- Good knowledge of MS Excel, Access and PowerPoint

- Experience with EDC systems

- Team player, able to work in an international environment

- Fluent in English

- Ability to motivate in a dynamic environment

- High personal integrity

Company Benefits:

- Being part of an International company

- Making a difference in people's live

- Opportunity to discover your own potential

- Market conform salary with interesting extra-legal advantages

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, Clinical Data Management, e-CRF development, data cleaning, EDC-systems experience, International environment, Medical Devices

Clinical Data Coordinator, Data Manager, eCRF

Apply for this job: Clinical Data 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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