About The Position

As a Principal Clinician – IR/IRev at Clario, you will play a critical role in ensuring the integrity and quality of clinical trial data. This position focuses on conducting independent reviews of psychiatric and neurocognitive assessments to support global clinical studies. You will work closely with site raters and internal teams to maintain compliance with Good Clinical Practice (GCP) and study protocols, helping accelerate the delivery of life-changing therapies to patients. 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. EEO Statement Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic. Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.

Requirements

  • Education: Master’s or Medical degree in Psychology, Social Work, Counseling, Psychiatric Nursing, or related healthcare discipline.
  • Experience: Minimum 2 years diagnosing/treating psychiatric or neurocognitive disorders; experience with standardized assessment tools preferred.
  • Skills: Strong communication, proficiency in MS Office, and knowledge of GCP guidelines.
  • Certifications: Relevant clinical certifications may be required based on study protocols.

Responsibilities

  • Independent Review (IR/IRev): Evaluate and score site assessments using standardized diagnostic and symptom rating scales.
  • Data Quality Assurance: Ensure compliance with GCP, study protocols, and SOPs.
  • Training & Calibration: Conduct training sessions for site raters and participate in calibration exercises.
  • Collaboration: Work closely with clinical operations and project teams to maintain protocol adherence.
  • Technology Utilization: Use remote assessment tools and submit accurate data.

Benefits

  • Competitive compensation
  • Medical, dental, and vision insurance beginning Day 1 of employment
  • Flexible work schedules
  • Attractive PTO plan
  • Engaging employee programs
  • Remote working

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What This Job Offers

Job Type

Full-time

Career Level

Principal

Number of Employees

1,001-5,000 employees

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