Jobs in Avignon, France

Remote, France

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life‑changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease.

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 now recruiting Clinical Research Associate I/ Clinical Research Associate II to join our team in France. This is a remote‑based position with travel to sites for morning visits. Candidates should be based in Paris or the Paris area.

• Calm, thoughtful, and responsive when things don’t go as planned.
• Well‑prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
• Finds quick and creative ways of overcoming difficulties.
• Has an impeccable eye for detail.
• Identifies potential study risks and proposes solutions on how to mitigate them.
• Takes responsibility for the quality and outcomes of your work.
• Is adept at handling conflict by using tried and true resolution strategies.

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; help prepare regulatory submissions, conduct pre‑study and initiation visits, etc.).

• Life science degree and/or equivalent experience.
• 1 year or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management or equivalent experience in clinical research.
• Experience managing oncology studies.
• Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions).

• Excellent communication and organizational skills are essential. A team player.
• Evidence of a client‑focused approach.
• 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 the country where the position is based.

Study start‑up activities experience.

Please apply in English.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.