.Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world's most challenging health concerns. Our Clinical Research team, who powers our PPD clinical research portfolio, are part of our leading global contract research organization (CRO). Clinical Research Associate - Client-dedicated - Andalucia Who is PPD Clinical Research Services? PPD is a leading global contract research organization. Our purpose is to improve health. Our mission is to help customers deliver life-changing therapies. Our strategy is to bend the cost and time curve of drug development and optimize value for our customers. PPD is now part of Thermo Fisher Scientific. As the world leader in serving science, our Mission is to enable our customers to make the world healthier, cleaner and safer. We are excited about the opportunities this combination brings to enhance our comprehensive end-to-end offering, enabling customers to move rapidly from scientific idea to approved medicine. The PPD FSP Solution: PPD's Functional Service Provider division partners with and serves as an extension of our PPD team, supporting our customers' key functions. We cover customer needs on every level, allowing them to do more with less, with an uncompromising commitment to quality. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success. Joining within our PPD FSP functional area allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience. Responsibilities include but are not limited to: Monitoring independently different sites, including RBM. Participation in investigator meetings as necessary. Ensuring the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, SOPs, etc. Ensuring effective communication between investigational sites and internal/external stakeholders. Working on project work and initiatives for process improvement as required. Requirements: Education and Experience: Degree in pharmacy, life science or related field. Experience in a pharmaceutical, biotech or CRO company. Independent clinical monitoring experience - at least 1 year. Fluency in English and Spanish. Knowledge, Skills and Abilities: Demonstrated understanding of medical/therapeutic area knowledge and medical terminology. Management of regulatory and/or IEC questions. Development and preparation of the local informed consent form. Effective oral and written communication skills, with the ability to communicate effectively with medical personnel. Management of the delivery of study supplies. Strong customer focus. Effective interpersonal skills. Strong attention to detail. Effective organizational and time management skills