CROMSOURCE

Freelance Clinical Research Associate - Luxembourg - L

4 days left

Company
CROMSOURCE
Location
Luxembourg
Salary
Competitive
Posted
12 Apr 2021
Closes
12 May 2021
Ref
HQ00002490
Discipline
Clinical Research
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)
Description:
CROMSOURCE is currently recruiting for a Clinical Research Associate for an internal position.

In this role you will be working in with our in-house team. You will be responsible for full site management from feasibility to close out of studies. We have a varied client base, ranging from small-mid sized Pharma and Medical Device companies.The site will be based in Luxembourg but we are willing to consider applicants based near the borders from France or Belgium.

Position Duties & Responsibilities:
  • Assists in the selection of sites, site evaluation visits, initiation visits and ensuring follow up by obtaining the pre-study documentation to ensure good start-up of the investigation sites
  • Performs training of site staff in all study procedures in order to ensure protocol/ICHGCP compliance
  • Conducts and reports periodic monitoring visits in the field and reviews at each visit accuracy, legibility, completeness and quality of Case Report Form (CRF) in compliance with the protocol, SOP's and ICH-GCP requirements in order to ensure data integrity and subject safety
  • Adapts and translates Patient Information Leaflets and Informed Consent Forms
  • Cooperates with the site staff for ensuring a proper reporting from the site of the safety issues (adverse events and adverse reaction such as AEs/SAEs, SUSARs, etc.) and their follow up, guaranteeing timely and appropriate handling of safety issues
  • Escalates any issues to relevant project team members
  • May assist in contract negotiation with sites on study budget after appropriate and documented training
  • May support the submission process in the project (or region)


Education, Experience and Skills:
  • University Degree in scientific medical or paramedical discipline
  • Prior experience as a CRA
  • Excellent knowledge of clinical trial operations, ICH-GCP Guidelines and other applicable regulatory requirement
  • Fluent in English
  • 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=HQ00002490

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: CRA, Clinical Research Associate, Clinical Research, CRO, Clinical Research Organisation, Clinical Trials, Clinical, submissions, Clinical Research ICH-GCP, Monitoring, Home based Luxembourg Belgium France
Skills: Freelance, Clinical, clinical trials, CRO Location: Luxembourg Share:

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