Marie-Claude Morice, Andreas Grüntzig Ethica awardee

CERC is very proud to announce that its CEO Marie-Claude Morice, has received during EuroPCR 2021 the Andreas Grüntzig Ethica award, « in recognition of her outstanding ongoing contribution to training, education and clinical research in interventional cardiovascular medicine. » Relive this precious moment...

CERC at EuroPCR 2021

CERC is a long-standing partner of EuroPCR. In this year of change, there was no way we were going to miss the event! 2 CERC trials are presented: EBC MAIN (read pg. 2), a late-breaking trial, Wednesday, May 19, 10:20 – 10:40, Main Arena, « EBC MAIN – the European Bifurcation Club left main coronary bifurcation study” but also via a CERC interview with David Hildick-Smith, entitled « EBC Main: behind the curtain », available in the Videos On Demand section. Electroducer, a novel stimulation device (read pg. 3). This innovation was selected for the « Jon Dehaan Foundation Prize » competition. The presentation is available in an on-demand video entitled « Universal direct wire pacing (DWP) device to simplify THV and complex PC” and presented by Nicolas Dumonteil. Come and join us at EuroPCR...

Chronicle n°18, May 2021

Our latest studies and publications, our new services… Discover all the news for the first quarter of the year in the latest issue of our Chronicle. 👉Follow this...

Senior Regulatory Affairs Associate

Senior Regulatory Affairs Associate The European Center for Cardiovascular Research (CERC) is a CRO specialized in the design and management of international clinical trials dedicated to cardiovascular diseases. Chaired by four interventional cardiologists, actors of clinical research for over 20 years, the CERC conducted clinical studies directly in line with the issues of cardiologists practicing in private or public hospitals. CERC is currently supporting thirty studies for industrial promotions but also manages more than 10 “investigators initiated trials” whose purpose is the treatment of conditions / comorbidities for which there is no satisfactory therapeutic strategy. CERC is an Entreprise à Mission. CERC is currently looking for a Senior Regulatory Affairs Associate.   Job description You will be in charge of th Management of worldwide regulatory aspects of the CERC clinical studies and contribution to the maintenance of the CERC Quality and Process Management System, including: Ensuring that clinical studies applications are conducted according to local and international requirements/procedures Coordination and performance of the submission packages to CA and EC until approval Providing technical and regulatory expertise for the preparation of documents to be submitted Performance of regulatory intelligence, in collaboration with the Clinical Operations Manager Contribution to the maintenance of the CERC Quality and Process Management System Skills Degree in Scientific/Healthcare discipline Significant regulatory submission experience Professional English Good computer skill The position is available immediately and is based in Massy, Essonne (91), France 12 reasons for joining us👉 https://www.cerc-europe.org/12-reasons/     INTERESTED ? RESUME COVER...