Clinical Research Associate II/ Senior Clinical Research Associate

Precision Medicine Group; Mérignac; À distance; EUR 45 000 - 65 000; Plein temps

Résumé du poste

A leading Clinical Research Organization in France is seeking experienced CRA II or Senior CRA professionals to monitor Oncology clinical studies. This remote position involves coordinating site activities and ensuring compliance with protocols. The ideal candidate has a background in life sciences and at least one year of experience in Oncology. Opportunities for training and mentorship are available. Competitive travel arrangements are included.

Qualifications

• A minimum of 1 year experience as a CRA in Oncology.
• Availability for domestic and potentially international travel.
• Understanding of financial management for Senior CRA positions.

Responsabilités

• Monitor and own the progress of clinical studies at investigative sites.
• Coordinate activities for study setup and monitoring.
• Train and mentor junior staff.

Connaissances

Monitoring experience for Oncology clinical studies

Life science knowledge

Client interaction skills

Formation

Life science degree or equivalent experience

Description du poste

Overview

Precision for Medicine is not your typical CRO. We bring 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. 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 our culture and proud of extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the people and 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. Your voice will be heard; working in a smaller CRO allows you to have influence and support from direct line management.

We are looking for an experienced CRA II or Senior CRA to join our team in France. You will have previous monitoring experience for Oncology clinical studies in France and you will be located in Paris or the Paris area.

This is a remote based position with travel to sites for monitoring visits.

Responsibilities

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 opportunities 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.

Qualifications

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; 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

Please, apply in English.

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About Precision for Medicine

We invite you to learn more about our growing organization serving our clients that are researching ground breaking 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. We combine novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and a passion for rare diseases and oncology, in addition to working across other therapeutic areas.

We are committed to fighting cancer by linking specific mutations to specific treatments through biomarkers. We combine deep science with deep data from advanced platforms, then apply specialized expertise in the design and execution of targeted, adaptive clinical trials. We deliver robust insights that inform real-time decisions and optimize the oncology development pathway.

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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 [e-mail].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.