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Clinician Rater, Contractor

Trabajo disponible en: Palma, Balearic Islands, España
Empresa: Worldwide Clinical Trials
Contrato puesto
Publicado en 2026-07-01
Especializaciones laborales:
  • Servicios Médicos
    Investigación clínica, Ciencia Médica
Rango Salarial o Referencia de la Industria: 40000 - 60000 EUR Anual EUR 40000.00 60000.00 YEAR
Descripción del trabajo
Who We Are
We’re a global, 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

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