Senior CRA Home based

ICON Strategic Solutions; France; Hybride; EUR 40 000 - 55 000; Plein temps

Résumé du poste

A global pharmaceutical partner is seeking a Clinical Research Associate based in Paris. The role involves leading clinical studies with ownership of investigator sites and requires a minimum of 3-4 years of independent monitoring experience. Candidates should be fluent in French and adept at working in dynamic environments. This position offers an opportunity to contribute to life-changing treatments.

Qualifications

• Minimum 3-4 years of independent monitoring experience is essential.
• Experience as a CRA, preferably in oncology trials.
• Ability to prioritize and respond to changing business needs.

Responsabilités

• Full ownership of investigator sites for assigned studies.
• Planning and conducting various site visits per the clinical monitoring plan.
• Developing effective relationships with investigator site staff.

Connaissances

Independent monitoring experience

Fluency in French

Professional proficiency in English

Excellent organization skills

Strong IT skills

Strong communication skills

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 3-4 years 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

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