Clinical Research Associate 2 – Multisponsor – South of Spain

## About the role Join us in our exciting journey!! We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division. As an experienced Clinical Research Associate, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with our development opportunities. At IQVIA, you’ll have training and development to plan and progress your career in the direction you choose; we do not believe in a 'career ceiling.' IQVIA is expanding in Spain - we currently have multiple exciting vacancies for Clinical Research Associates 2 to work Full Services model to work with our key pharmaceutical clients. If you have independent site monitoring experience as CRA and want to discover how a true partnership between the CRO and sponsor works, then this is the right opportunity for you! Our clients are pharmaceutical companies who are dedicated and passionate about improving the lives of patients across several therapeutic areas. ## Responsibilities - Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plans. - Administer protocol and related study training to assigned sites and establish regular lines of communication. - Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations – escalating quality issues as appropriate. - Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution. - Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans ## Requirements - In depth knowledge and skill in applying applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines - In depth therapeutic and protocol knowledge as provided in company training - Excellent organizational and problem-solving skills - Effective time management skills - Strong written and verbal communication skills including good command of English and Spanish - Bachelor's degree in a health care or other scientific discipline or educational equivalent - 2-4 years of independent on-site monitoring experience ## Nice to Have - None specified ## Benefits - Working with one of the TOP 5 sponsors globally on international projects. - Focus on quality, not quantity! We invest in keeping our teams stable, so workload is consistent. - The chance to work on cutting edge medicines right at the forefront of drug development. - Genuine career development opportunities for those who want to grow as part of the organization. - Flexible conditions and an attractive remuneration package. - Office or home-based roles available!