Clinical Trial Educator (France)

Job Overview Acts as a strategic partner to both external and internal stakeholders. Leads the relationship management and communication of medical and scientific information with health-care providers, patients, care givers. Essential Functions * Responsible for maintaining clinical competence in various disease areas and technical knowledge of specialty areas. * Provides Education to Healthcare professionals and their staff, reinforces study protocols as related to clinical trials. * May have direct interaction with patients to offer education on trial, disease, and/or device/medication. Partner with referral networks to identify potential trial subjects. * Maintain and analyse customer records to customize strategies to maximize patient pre-screening, screening, enrolment in trials. * Completes internal electronic reporting system records. * Coordinate, plan, and host group events designed to optimize program delivery. * Maintains organization's equipment safely and in a good state of repair Qualifications * Bachelor's Degree Bachelor's Degree Req * Excellent interpersonal and communication skills; * High flexibility to travel, * Team player for the good of the team; upholding values of IQVIA and the CTE group, empathy and awareness of cultural differences. * Works to develop and raise the skill level of others; mentors, * Takes on additional responsibilities beyond their normal role. * Collaborative mentality; * Strong customer service approach; * Ability to quickly gain an understanding of a situation and to have a solutions based approach to resolving problems; "can-do-attitude"; * Ability to coordinate and complete activities across multiple functions; * Ability to execute tasks with minimal oversight; prepared to make considered decisions on own initiative; We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing international medical affairs division as a clinical trial educator. As our specialist CTE, you will be able to accelerate patient enrolment, improve site performance and help streamline studies in ways no other team member can. You’ll often be your sites’ go-to person for information, advice and problem solving. You will also have the chance to work on studies featuring complex or non-traditional patient pathways often featuring compressed timelines for diagnosis and enrolment and complex protocols requiring intense initial education and ongoing reinforcement. It will be your role to help to navigate issues where intense competition exists for similar patient populations. You will also be needed to provide regular training and assistance for site staff and patients on issues such as drug administration and testing. This position is fully HOME-BASED and we offer a FIXED-TERM CONTRACT for one year! If you would enjoy the following:- * Having a dynamic role which changes as the clinical trial progresses * Engaging with and educate clinical trials investigators and patients * Help to improving patient care Does this sound like you? Do you have what it takes? Our clients are pharmaceutical companies who are dedicated and passionate about improving the lives of patients across several therapeutic areas. Responsibilities: * Provide practical support to study sites to maximize potential for patient enrolment. * Work with research sites to identify and address recruitment barriers – identify common site issues and work with the sponsor and relevant stakeholders to recommend creative options to overcome these barriers. * Provide on-going training and information on the clinical trial inclusion and exclusion criteria to the study team, where required conduct training for new study staff. * Act as a resource for healthcare professionals at clinical study sites by sharing best practices and strategies for patient identification and retention. * Conduct recruitment training sessions * Identify patient flow / pathway through site and work with identified departments to raise awareness of protocols and the potential for patient inclusion. QUALIFICATIONS * Experience working in a Clinical Trial Environment. * Ability to coordinate activities across multiple functions and drive them to completion. * Have a solutions based approach to addressing the identified barriers to recruitment. * Good Business and Commercial acumen. * English and the local language is essential! * Ability to make rapid and accurate assessments. * Excellent interpersonal and communication skills. * Highly motivated well organized and results oriented. * Flexibility to travel both nationally and internationally. * Driving License required. * Eligibility to work full-time in the country where the position is advertised * Experience in therapeutic areas such as Pulmonary Arterial Hypertension, Cardiovascular, respiratory, Renal disease, Oncology At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com