At Medartis, we combine innovative solutions with skilled professionals to be the provider of choice in orthopaedics. Founded in 1997 and headquartered in Basel, Switzerland, the Medartis Group is one of the world’s leading manufacturers and providers of medical devices for the surgical fixation of bone fractures in the upper and lower extremities, as well as the craniomaxillofacial region. The company employs around 1,400 people across its 13 locations and sells its products in over 50 countries worldwide.
*Please note: The selected candidate will be required to relocate to Miami, Florida, by January 2028.*Your responsibilities Cultivate a portfolio of clinical research projects and a network of clinical research sites and investigators to support Medartis business and regulatory requirements Create new and maintain existing customer contacts to include visits, trainings and advice acting as the point of contact between internal and external partners Create new and maintain existing processes within the Medartis quality system ensuring that all processes comply with internal and external regulatory and legal requirements Select and support preclinical and clinical studies (including patient registries, retro- and prospective studies, case study reviews, pre-clinical modeling, possible PMA studies, etc.) byproactive engagement of study institutions and clinical researchers to participate in studiesdirecting communication with the study director from the conception phase until publication of the final report, providing support withwriting of study protocols contractual questions and follow up as requiredregulatory requirements (lRB, ethics committees, ICH-GCP, ISO 14155, SAE reporting)statistical analysis and scientific writing (written reviews for publication/ presentations)implementation of digital tools such as databases, EDC solutions, registries, (e)CRFs, etc. and training of study staff (nurses, PIs, etc.) on said toolssupplying study hardwarecoordination with CROspreparation and maintenance of TMF and ISFsupport of study site(s) and study nurse(s); e.g., with questions relating to data entryvisits and/or on-site monitoring of study sitestimely communication with all relevant regulatory bodies/lRBsstudy follow up and data collection with Responsible for the complete development of study protocols that meet FDA clearance standards, maintain the continuum of support documentation to further validate the proper ‘Indications for Use’ via education and training on the future and existing Medartis product offerings Conscientious, careful, punctual, and reliable work approach Fast comprehension and ability to quickly familiarize oneself with new subject areas Can work independently and motivated in a small group of specialized experts Willingness to take initiative and act autonomously Demonstrates assertiveness and patience in daily work Relationship development in settings of the field, labs, conferences, or dinner meetings Conscientious, precise communication Degree in a STEM field at a university level or equivalent professional experience/training; PhD and GCP certificate desirable Familiar with logistical and regulatory issues in the field of clinical studies Familiarity with the field of orthopedic surgery or orthopedic medical device design preferred Knowledge of statistics is advantageous Proficient in office applications Familiarity with EDC software solutions is advantageous Scientific, structured, rigorous, and strategic work approach Willingness to travel (up to 20%)Fluent (spoken and written) in English, other languages are advantageous
What we offer:
This is an integral, responsible and diversified role with a focus on quality and service provision in a rapidly growing, international company. For further information please visit our Website www.medartis.com.
