Central Quality Reviewer - Digital Health Science

Signant Health; Galapagar; A distancia; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading company in digital health is seeking a Central Quality Reviewer to oversee data quality and ensure compliance with clinical standards. This role involves clinical analysis, training support, and collaboration with clinical teams to enhance study outcomes. Ideal candidates will possess advanced healthcare qualifications and demonstrate strong analytical and communication skills, thriving in a remote, multicultural environment.

Servicios

Competitive compensation and benefits

Remote working flexibility

Growth opportunities in a collaborative environment

Formación

• Master’s or similar qualification with clinical experience in psychiatric or cognitive scales.
• Excellent communication skills in English, both written and spoken.
• Ability to work effectively in a remote, multicultural environment.

Responsabilidades

• Conduct activities in compliance with Good Clinical Practice guidelines.
• Evaluate submitted data and provide feedback.
• Monitor and review the quality of CQR activities.

Conocimientos

Attention to detail

Analytical skills

Organizational skills

Problem-solving skills

Communication skills

Educación

Master’s Degree or similar healthcare-related qualification

Bachelor’s degree or RN with two years of relevant experience

Descripción del empleo

Central Quality Reviewer - Digital Health Science

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Want to do the Best Work of Your Life?

Working at Signant Health places you at the heart of a high-growth, dynamic sector within an innovative industry. We are transforming the clinical trial landscape through cutting-edge technology, innovation, and exceptional service delivery.

Where do you fit in?

The Central Quality Reviewer (CQR) is responsible for delivering services and tasks that meet defined requirements and align with company strategic objectives. The CQR oversees data quality for Signant Health’s Rater Training, Endpoint Reliability, and Quality Assurance programs. Responsibilities include clinical analysis of scales used as study endpoints, ensuring administration and scoring calibration adhere to training principles and best practices. The CQR may also conduct investigator communications, provide independent scoring of audio / video files, and support site training and calibration efforts.

Main responsibilities include :

• Conduct activities in compliance with Good Clinical Practice guidelines.
• Assist in training, calibration exercises, and quality control procedures.
• Evaluate submitted data, contact raters for clarification, and provide feedback.
• Ensure review consistency, resolve ambiguities collaboratively, and document review processes.
• Possibly interview study subjects or provide independent scoring based on audio / video review.
• Monitor and review the quality of CQR activities and performance indicators.
• Collaborate with the clinical team to prepare for study start-up, including onboarding and training materials.
• Identify and escalate potential issues proactively.
• Support site relationship development to ensure training and calibration standards.
• Communicate feedback and instructions effectively with site staff.

Qualifications required :

• Master’s Degree, M.D., Ph.D., Psy.D, Pharm.D., or similar healthcare-related qualification with at least one year of clinical experience involving psychiatric or cognitive scale administration, OR a Bachelor’s degree or RN with two years of relevant experience.
• Comfort with investigator and peer remediation.
• Strong attention to detail.
• Ability to work effectively in a remote, multicultural environment.
• Excellent analytical, organizational, and problem-solving skills.
• Deep knowledge of psychiatric and / or cognitive scales.
• Basic statistical knowledge and data interpretation skills.
• Excellent communication skills in English, both written and spoken.

Our ways of working for success :

• Problem-solving mindset with a positive attitude.
• Motivated by working in a fast-paced, global environment.
• Self-driven, eager to learn and grow.
• Excellent communication skills, able to articulate technical details clearly.
• Knowledge sharing to promote organizational learning.

Why join Signant Health?

• Contribute to clinical research innovation.
• Work in a collaborative, fast-paced environment with growth opportunities.
• Enjoy competitive compensation and benefits.
• Benefit from remote working flexibility.
• Join a global team dedicated to improving patient outcomes.

Ready to elevate your career? Apply today!

At Signant Health, we celebrate diversity and are committed to equal opportunity employment regardless of race, gender, age, disability, or background.

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