Cta 1 & 2, Portugal

**Join us in our exciting journey**: We currently require a motivated and enthusiastic clinical trials professional to join our rapidly growing international division as a Clinical Trials Assistant. **This position is office-based (flexible) and we offer a fixed-term contract for one year** Our client is one of the TOP 5 pharmaceutical companies who is dedicated and passionate about improving the lives of patients across several therapeutic areas. **The role: Responsibilities** Provide administrative support to clinical projects and update clinical systems and databases. Assists with general administrative functions, as required, in support of designated clinical team members. - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines. - Collaborate on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files and completeness. - Collaborate on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. - Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. - Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. - Assist in training and orienting new staff. May act as a mentor for less experienced CTAs. - May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval. - Perform assigned administrative tasks to support team members with clinical trial execution. - Previous experience with within CTA role, namely: study documents preparation, maintenance and archive. - Experience with study payments issues & regulatory submission is not mandatory but will be a plus. - Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. - Knowledge of applicable protocol requirements as provided in company training. - Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint - Effective written and verbal communication skills - Effective time management and organizational skills - Ability to establish and maintain effective working relationships with coworkers, managers and clients - Good command of English language **We invite you to join IQVIA** - Recognized by **Great Place to Work** as the second best company to work for in Spain (March 2019) - ** FORTUNE Magazine's World's Most Admired Companies** list for the third year in a row. - Recognized by the 2016 Scrip Awards as the **Best Full-service Provider Contract Research Organization** (CRO) - Awarded the 2016 Eagle Award from the Society for Clinical Research Sites (SCRS) for the fourth consecutive year. - A site-nominated award recognizing contract research organizations (CRO) and biopharmaceutical sponsors dedicated to **building positive relationships with research sites through leadership, professionalism and integrity**. - IQVIA named in The International Association of Outsourcing Professionals (IAOP) 2017 Global Outsourcing 100® List which recognizes the world’s best service providers across a range of industries. IQVIA is an **equal opportunity employer**. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status.“ We know that meaningful results require not only the right approach but also the right people. Regardless of your role, **we invite you to reimagine healthcare with us**. You will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there