Job DescriptionCompany IntroductionOur client leads the pharmaceutical world markets by providing high-quality healthcare systems for a variety of customers in the United States. Their extensive experience enabled them to build long-lasting partnerships with major companies around the world while adapting their services to the needs of their clients. Since their foundation, innovation has been a driving force for the company thanks to their team's ability to always find and exploit innovative ideas.RoleJob Overview: You will be a key member of the pharmaceutical research department, working with a team to ensure that the company's services meet quality standards in the United States. You will also help monitor and regulate the efficiency of the department's services, ensuring an optimal pace for all core and ad-hoc activities.You will also be expected to work with other departments to meet research project requirements; Deal with information discrepancies, update research registries, procedures, and tools as well as provide reports about the progress of each project.Responsibilities and Duties:•Supervise study sites and activities to ensure adherence to appropriate industry protocols and terms of the study.•Collect and authenticate data collection forms otherwise known as case report forms.•Screen potential study participants through medical record reviews, interviews, and follow-ups with healthcare providers.•Coordinate with ethics committees to safeguard the rights, safety, and well-being of all research subjects and research activities.•Maintain specific records of research activity including regulatory forms, drug dispensation records, case reports, and consent forms.Profile Requirements•Fluency in English is a must; previous professional anglophone experience is a plus.•At least a bachelor's degree in pharmaceutics or any relevant discipline is necessary.•At least 5 years of work experience as a clinical research associate or a similar role.•Must possess superior analytical and creative thinking skills.•Excellent attention to detail and the ability to keep detailed, accurate records.•Strong written and verbal communication skills.If you are interested, kindly send your CV in English to: