Senior CRA Home based

ICON; Paris; À distance; EUR 45 000 - 60 000; Plein temps

Résumé du poste

A global clinical research organization is seeking a Clinical Research Associate in Paris. This role entails full ownership of investigator sites, planning site visits, and ensuring data integrity. The ideal candidate has 3-4 years of CRA experience, is interested in oncology trials, and possesses strong communication and organizational skills. Fluency in French and professional proficiency in English are required.

Qualifications

• Minimum 3-4 years of experience as a CRA.
• Interest in oncology trials.
• Fluency in French and professional proficiency in English.

Responsabilités

• Full ownership of investigator sites for assigned studies.
• Planning and conducting site visits in accordance with the clinical monitoring plan.
• Develop relationships with investigator site staff.
• Prepare for and attend investigator meetings.
• Ensure integrity of clinical data.

Connaissances

Independent monitoring experience

Strong organization skills

Strong IT skills

Strong communication

Multitasking

Description du poste

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 3-4years of independent monitoring experience is essential

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

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

#LI-KD1