Description:
Job Title: Clinical Study Coordinator

Location: Paris, France

Schedule: Full Time, Freelance

TalentSource Life Sciences, the division of CROMSOURCE dedicated to flexible staffing solutions, is currently searching for an experienced freelance Clinical Study Coordinator to join one of our partner companies - a leading international pharma company - in Paris, France.

This will be a full time, office based position and the successful candidate will be working on studies dedicated to one client.

As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts.

Main Responsibilities:

• Patient inclusion: prepare visits, pre-visit screenings, patient assistance during visits, questionnaires, e-CRF completion
• Manage the creation, maintenance and archiving of the Investigator Site Files (ISF)
• Maintain and track all site related clinical trial documentation ensuring they meet Good Clinical Practice (GCP) guidelines
• Plan, coordinate and assist with site selection and site initiation visits
• SAE reporting
• Updating/maintaining eCRF

Requirements

• Bachelor's degree in a scientific or related field
• Previous experience in a similar role as a Project Assistant, Clinical Trial Assistant, Study Coordinator or similar
• Good knowledge of GCP
• Possesses good communication and organizational skills

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.

About TalentSource Life Sciences

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having the continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role and work autonomously.

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.

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.

Key words: Study Coordinator, Clinical Coordinator, Clinical Research Associate, CRA, Freelance CRA, Freelance, Freelancer, Contract, Full Time, CRO, Contract Research Organization, Outsourced, Pharmaceutical, Consultant

Skills: Clinical Study Coordinator Location: France Share:

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