Clinical Research Associate / Senior Clinical Research Associate

Precision Medicine Group; France; À distance; EUR 40 000 - 60 000; Plein temps

Résumé du poste

Join a forward-thinking Clinical Research Organization dedicated to advancing oncology therapies. In this remote role, you will leverage your expertise as a Clinical Research Associate to monitor clinical studies and ensure compliance with protocols and regulations. With a focus on quality and detail, you will be instrumental in identifying study risks and proposing solutions. This position offers the opportunity to influence clinical trial outcomes while enjoying a balanced work-life environment. If you are passionate about making a difference in cancer research and thrive in a collaborative setting, this role is perfect for you.

Qualifications

• Minimum of 1 year experience as a CRA in Oncology required.
• Experience in monitoring clinical studies and regulatory submissions.

Responsabilités

• Monitor and ensure clinical studies are conducted per protocol and regulations.
• Coordinate activities for study setup and monitoring visits.

Connaissances

Clinical Research

Oncology Knowledge

Monitoring Experience

Conflict Resolution

Attention to Detail

Formation

Life Science Degree

Graduate/Postgraduate Degree in Scientific Discipline

Description du poste

Clinical Research Associate / Senior Clinical Research Associate

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 looking for an experienced CRA or Senior CRA to join our team in France. You will have previous monitoring experience for Oncology clinical Studies in France.

This is a remote based position (homebased anywhere in France), with travel to sites for monitoring visits.

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.).

Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope. You will also have the opportunity to train and mentor junior staff members. You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.

Requirements:

• Life science degree and / or equivalent experience
• CRA experience within the CRO or pharmaceutical industry (and working in Oncology). We require a minimum of 1 year experience as a CRA in Oncology, and can offer CRA II and Senior CRA titles depending on experience level.
• Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)

Preferred:

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
• Two+ years of oncology experience
• Study start up activities experience would be an advantage
• For Senior CRAs, understanding of financial management and mentoring experience would be desirable

We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.

About Precision for Medicine:

Precision for Medicine is a precision medicine Clinical Research Organization. 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, in addition to working across other therapeutic areas.

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.