Clinical Research Associate H/F

Paris /
CLQARA – Clinical /
CDI statut cadre
/ Hybrid
🫀Who we are?

Improving the lives of patients suffering from Atrial Fibrillation (a pathology causing an irregular heart rate) thanks to artificial intelligence ? It is possible ! 

The creation of Volta Medical follows the discovery of a new complex medical procedure to treat atrial fibrillation (the most common cardiac arrhythmia in the world) by the company’s founders, world experts in interventional rhythmology and intracardiac signal analysis. 

Volta Medical is an innovative start-up based in Marseille, whose goal is to provide a range of artificial intelligence-based products to guide the cardiologist during ablation-type procedures.

We started this adventure 7 years ago and our team now has nearly 70 employees in France, Germany and the United States ! We completed a $27 million Series A round in November 2020 and a $36 million Series B round in January 2023.

🫀Our values

    • Be a pioneer: Be brave. Don’t be scared of researching, exploring, trying and sometimes failing.
    • Improve patients’ lives: Create products to provide electrophysiologists with the best user-experience possible, to help them improve the lives of patients.
    • Strive for excellence: Push yourselves to deliver the highest quality in everything you do. Learn from your mistakes and aim for the best.
    • Collaborate as a team: Welcome to a multidisciplinary and a diversified team ! Try to understand people from different cultures and environments. Confront your ideas and have fun !


    • You will be working in the Clinical Affairs team, in close proximity with the Clinical Project Managers : 

    • Monitor clinical sites in France and in Germany for all types of studies (research, pre-market, post-market)
    • Assist in the development of document templates, relevant SOPs and guidelines
    • Work closely with clinical personnel and the PI to ensure that clinical documents are produced to the standard required by GCPs
    • Ensure accurate and complete documentation of all clinical study source documents and/or forms according to Volta's SOPs, GCPs and other applicable guidelines and regulations (MDR, CSP)
    • Conduct all work in compliance with SOPs, GCP and regulatory requirements
    • Compile study documents
    • Assist Clinical, Regulatory and Quality teams as required.

🫀 Profile

    • Bachelor's or master's degree in Life Sciences
    • At least 3 years of experience in a similar role in CRO/Industry/Hospital 
    • Clinical Research experience and GCP knowledge are mandatory
    • Cardiology and/or Medical Device experience is a plus
    • Fluency in French, advanced in English and/or German
    • Excellent interpersonal and communication skills
    • Attention to detail and scientific accuracy  

    • At Volta Medical, we are convinced that diversity and inclusion are real strengths for the company. Our opportunities are open to all, we encourage you to apply !

🫀 What we can offer you at Volta Medical

    • A fixed gross compensation ranging between 40 and 50 K€ a year as well as a variable part, both depending on your profile 
    • A pleasant work environment, with ideally located offices in the 6th district of Marseille offering a magnificent view upon Notre Dame de la Garde and the Mediterranean Sea. 
    • The possibility of working from home 2 days a week
    • Passionate colleagues that have the same goal in mind: improve patients’ lives
    • A corporate culture based on innovation, empowerment and collaboration.
    • An international environment that allows you to practice your best american accent
    • Prospects of ambitious evolutions with various internal mobilities
    • Regular team building events, breakfasts for gourmands and for the people enjoying sport activities, free weekly yoga classes and preferential rates for a gym subscription.
    • And more traditional advantages: a lunch voucher card (Swile), a good health insurance (Malakoff Humanis), a vacation bonus, RTTs in addition to paid vacation, as well as exceptional days of absence on top of those provided in the collective agreement (compensation hold in case of illness starting from 6 months of seniority, additional days for a sick child, moving leave, etc.) 

    • Join a company on a human scale, whose operations leave room for initiative and innovation in the service of patients.

🫀 Our recruitment process

    • Interview with the N+1
    • Technical test/Situational setting 
    • Reference Check
    • Culture fit interview with a member of the HR team and a Volta ambassador
The information that you provide is subject to personal data processing by Volta Medical as data controller for the purpose of managing your job application. 
The information provided is for the use of Volta Medical’s recruitment team as well as other recipients (individuals and organizations) involved in the recruitment for the position that you applied for. Your information will be stored for the duration of the processing of your application. If you are not selected for the position, your information will not be stored, unless you consented to being included in our applicant database. In this case, your information will be stored for 2 years from the date of the submission of your application to enable us to contact you for future opportunities. Nevertheless, you have the right to withdraw your consent at any time.
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