Who We AreWe’re a general, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why WorldwideWe believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join usWhat The Clinician Rater Does At Worldwide Clinical TrialsThe Clinician Rater is responsible for all aspects of assigned projects, including clinical assessment, training development, and data review for Worldwide Clinical Trials, Inc. (Worldwide). The Clinician works under the direction of the Director, Clinical Assessment Technologies (CAT).
What You Will DoThe Clinician is responsible for the clinical aspects of CAT projects as assignedApplies a working knowledge of clinical assessments to the development of training materialsReviews study‑specific assessment‑related data, as defined in the training plan,



to determine subject eligibility and contacts sites for data clarification and review outcomesTracks data reviews and provides monthly reporting to the sponsor and study teamReviews rater data to identify rater or data errors and is responsible for tracking, reporting, and reconciling errorsDemonstrates experience with clinical research and the utilization of clinical assessment measuresDevelops and manages training plans, data review plans, schedules, and timelinesDevelops and oversees data review activities and dissemination of data review findingsConducts research into scale acquisition and coordinates with Worldwide and sponsors to obtain licensesAssists in the review of electronic Clinical Outcome Assessment (eCOA) and electronic Patient‑Reported Outcome (ePRO) specifications and participates in User Acceptance Testing of equipment and programsResearches and contacts content experts to coordinate trainingsDevelops training materials under the guidance of the Director of Clinical Projects, CATDevelops and reviews presentations for adherence to template design and consistencyConducts remote scoring and assessments as appropriateCommunicates with study site staff regarding data quality issuesPrepares drafts of clinical content for training and qualification programs in clinical trials and reviews clinical deliverables as appropriateContributes to research effortsConducts patient interviews, prepares scoring rationale,



and coordinates the establishment of score rangesReviews and provides feedback on protocols and Case Report Forms (CRFs)Approves and ensures the quality of clinical contentAttends regular client meetings and Investigators’ Meetings to assist with the execution of training as appropriateTravels to sites for motivational visits and monitoring of clinical assessments as appropriateCollaborates internally and externally to ensure appropriate study designWrites and performs quality control reviews of final reports, white papers, and other scientific textsParticipates in training and ongoing synchronization of external Clinical ExpertsConducts training for Worldwide staff and investigators as appropriatePerform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all‑inclusive.
What You Will Bring To The RoleStrong organizational and management skillsClear understanding of best business practices related to rater training, methodologies, and corporate disciplineStrong planning, strategizing, managing, monitoring, scheduling, and critiquing skillsExcellent written and verbal communication skillsStrong interpersonal skills in a fast‑paced, deadline‑oriented, and changing environmentExcellent ability to manage multiple tasks and administrative details in a constantly changing environmentAbility to exercise sound judgment and make decisions independentlyStrong self‑motivation skillsProficiency in Microsoft Office applications, including Word, Excel, and PowerPointYour ExperienceMaster’s degree, M.
D., Ph.
D., PsyD, or Pharm.
D. in a healthcare‑related field with one year of clinical experience, including administration of psychiatric and/o

📌 Consultant, Clinician (Alcalá de Henares)
🏢 Worldwide Clinical Trials
📍 Alcalá de Henares