Associate Clinical Scientist

Clario; United Kingdom; Hybrid; GBP 40,000 - 65,000; Full time

Benefits offered by this job

Competitive compensation and incentives

Private health insurance

Flexible time off

Hybrid work options

Modern technology for remote collaboration

Remote collaboration tech

Job summary

A leading healthcare technology firm in the UK is seeking an Associate Clinical Scientist to join their eCOA team. This role involves shaping electronic clinical assessments for global clinical trials. Candidates should have a relevant degree and experience with assessment tools. The position allows for hybrid work and offers competitive compensation along with excellent benefits, including private health and flexible time off.

Qualifications

• Minimum 2 years administering standardized assessment tools and psychiatric rating scales.
• Knowledge of scale development and clinical assessment best practices.
• Basic understanding of Good Clinical Practice (GCP).
• Knowledge of scale development and clinical assessment best practices.
• Experience in clinical trials, research, or clinical settings preferred.
• Ability to work in fast-paced environment and manage multiple projects.
• Fluency in English; additional languages an asset.

Responsibilities

• Support development of clinical assessments from paper to eCOA formats.
• Conduct literature reviews and collaborate with subject matter experts.
• Coordinate to produce eCOA documentation for form builds.
• Assist in reviewing data from eCOA platforms to improve functionality.
• Maintain internal tracking for eCOA builds, documentation, and enhancements.
• Partner with operational teams during testing, validation, and issue resolution.
• Draft and update SOPs and process guidelines ensuring GCP compliance.
• Participate in team meetings and maintain communication with remote colleagues.

Skills

Administration of standardized assessment tools

Problem-solving skills

Collaborative teamwork

Fluency in English

Collaboration / teamwork

English fluency

Education

Bachelor’s degree in a relevant field

Graduate degree in psychology, social work or related field

Tools

MS Word

Excel

Adobe

Job description

As an Associate Clinical Scientist within our eCOA team, you will help shape the development of electronic clinical outcome assessments used in global clinical trials. This is an opportunity to apply your clinical assessment knowledge while working with innovative technology that improves data accuracy and enhances the patient experience. You’ll collaborate with experienced Clinical Scientists and cross‑functional teams to bring validated clinical instruments into digital formats that support high‑quality evidence and accelerated therapies.

What We Offer

• Competitive compensation and incentives
• Private health, pension, and life insurance
• Flexible time off and hybrid work options
• Engaging employee programmes
• Modern technology for remote collaboration

What You’ll Be Doing

• Support the development and migration of clinical assessments from paper to eCOA formats
• Conduct literature reviews and collaborate with internal and external subject matter experts
• Coordinate with internal teams to produce eCOA documentation for form builds
• Assist in reviewing data from eCOA platforms, usability testing, independent ratings, and surveys to improve functionality and clinical guidance
• Maintain internal tracking for eCOA builds, documentation, and enhancements
• Partner with operational teams during testing, validation, and issue resolution
• Draft and update work instructions, process guidelines, and SOPs that ensure compliance with GCP and internal standards
• Participate in team meetings and maintain consistent communication with remote colleagues

What We Look For

• Bachelor’s degree in a relevant field; graduate degree in psychology, social work, counselling, psychiatric nursing, or related field preferred
• Minimum 2 years administering standardized assessment tools, psychiatric symptom rating scales, and/or neurocognition scales (academic practicum from a terminal Master’s acceptable)
• Knowledge of scale development and clinical assessment best practices
• Experience in clinical trials, research, or clinical settings preferred
• Ability to work effectively in a fast‑paced environment and manage multiple projects
• Strong follow‑through, problem‑solving skills, and demonstrated initiative
• Ability to work collaboratively within multifunctional teams
• Fluency in English; additional languages an asset
• Basic understanding of Good Clinical Practice (GCP)
• Proficiency in MS Word, Excel, and Adobe
• Based in or able to work remotely from the United Kingdom

At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life‑changing therapies to patients faster.