Senior CRA Home based

Remote from: France
Annual salary: Undisclosed
Salary information is not provided for this position. Check our Salary Directory to estimate the average compensation for similar roles.
Department: Healthcare & Medical
Employment type: Full Time,
Job posted: 13 Aug 2025
Apply before: 13 Sep 2025
Experience level: Senior
Views / Applies: 12345 / 123

About company

About ICON plc

Accelerate the development of drugs and devices that save lives and improve quality of life

Research
Dublin, Ireland, 1990

Actively Hiring

Overview

As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical partners — a collaboration built on shared values of innovation, flexibility, and a joint mission to bring life-changing treatments to patients faster.

This is your opportunity to be part of an exclusive, high-impact program where you can lead by example and shape the standard for clinical excellence.

Location: Paris-based role – home based
Profile: We welcome experienced CRA professionals from both CRO and pharma sector backgrounds
Requirement: Minimum 3-4 years of independent monitoring experience is essential

Responsibilities

Key responsibilities include:

Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out
Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan
Developing effective relationships with investigator site staff to ensure that key clinical metrics are met
Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues
Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines

Qualifications

You will need:

A first stable experience as a CRA (min 3-4 years)
Interested in oncology trials
Excellent organization skills
Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
Strong IT skills
Strong communication with the ability to multitask and work effectively under pressure
Fluency in French and professional proficiency in English

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