Who We Are

We'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 Worldwide We 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 us
What The Clinician Rater Does At Worldwide Clinical Trials The 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 Do The Clinician is responsible for the clinical aspects of CAT projects as assigned
Applies a working knowledge of clinical assessments to the development of training materials
Reviews study‐specific assessment‐related data,



as defined in the training plan, to determine subject eligibility and contacts sites for data clarification and review outcomes
Tracks data reviews and provides monthly reporting to the sponsor and study team
Reviews rater data to identify rater or data errors and is responsible for tracking, reporting, and reconciling errors
Demonstrates experience with clinical research and the utilization of clinical assessment measures
Develops and manages training plans, data review plans, schedules, and timelines
Develops and oversees data review activities and dissemination of data review findings
Conducts research into scale acquisition and coordinates with Worldwide and sponsors to obtain licenses
Assists 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 programs
Researches and contacts content experts to coordinate trainings
Develops training materials under the guidance of the Director of Clinical Projects, CAT
Develops and reviews presentations for adherence to template design and consistency
Conducts remote scoring and assessments as appropriate
Communicates with study site staff regarding data quality issues




Prepares drafts of clinical content for training and qualification programs in clinical trials and reviews clinical deliverables as appropriate
Contributes to research efforts
Conducts patient interviews, prepares scoring rationale, and coordinates the establishment of score ranges
Reviews and provides feedback on protocols and Case Report Forms (CRFs)
Approves and ensures the quality of clinical content
Attends regular client meetings and Investigators' Meetings to assist with the execution of training as appropriate
Travels to sites for motivational visits and monitoring of clinical assessments as appropriate
Collaborates internally and externally to ensure appropriate study design
Writes and performs quality control reviews of final reports, white papers, and other scientific texts
Participates in training and ongoing synchronization of external Clinical Experts
Conducts training for Worldwide staff and investigators as appropriate
Perform 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 Role Strong organizational and management skills
Clear understanding of best business practices related to rater training, methodologies, and corporate discipline
Strong planning, strategizing, managing, monitoring, scheduling, and critiquing skills
Excellent written and verbal communication skills
Strong interpersonal skills in a fast‐paced, deadline‐oriented, and changing environment
Excellent ability to manage multiple tasks and administrative details in a constantly changing environment
Ability to exercise sound judgment and make decisions independently
Strong self‐motivation skills
Proficiency in Microsoft Office appl

📌 Clinician Rater, Contractor (Palma)
🏢 Worldwide Clinical Trials
📍 Palma