Senior Clinical Research Associate (France)

Precision Medicine Group; France; À distance; EUR 45 000 - 70 000; Plein temps

Résumé du poste

A leading company in precision medicine is seeking a Senior Clinical Research Associate based in France for a fully remote position. This role requires a strong background in clinical research with an emphasis on attention to detail and conflict resolution skills. You will ensure that clinical studies meet regulatory standards while maintaining high-quality outcomes, supporting your growth within a supportive and engaged work culture.

Qualifications

• At least 4 years of CRA experience within the CRO or pharmaceutical industry.
• Availability for domestic travel up to 50-60%.

Responsabilités

• Monitor and own the progress of clinical studies at investigative sites.
• Ensure studies are conducted per protocol, SOPs, and regulations.
• Coordinate necessary activities for study setup and monitoring.

Connaissances

Attention to detail

Conflict resolution

Problem-solving

Formation

4-year college degree or equivalent experience

Graduate or postgraduate degree in a scientific or healthcare discipline

Description du poste

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Senior Clinical Research Associate (France), remote, france

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EU work permit required:

Yes

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Job Reference:

3f8c101296ec

Job Views:

14

Posted:

23.06.2025

Expiry Date:

07.08.2025

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Job Description:

Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.

We are hiring a Senior CRA, this position will be fully home based working in France.

About you:

• You are calm, thoughtful, and responsive when things don’t go as planned.
• You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
• You find quick and creative ways of overcoming difficulties.
• You have an impeccable eye for detail.
• You identify potential study risks and propose solutions on how to mitigate them.
• You take responsibility in the quality and outcomes of your work.
• You are adept at handling conflict by using tried and true resolution strategies.

How we will keep you busy and support your growth:

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).

Qualifications:

• 4-year college degree or equivalent experience

Other Required:

• At least 4 years CRA experience within the CRO or pharmaceutical industry.
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
• Fluency in English and for non-English speaking countries the local language of country where position based

Preferred:

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline

Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.